รถพลังงานไฟฟ้า New 2021 MG EP (2021 เอ็มจี อีพี) มาพร้อมกับราคาค่าตัวที่ 988,000 บาท คำถามคือเงินก้อนประมาณ
2020 Proton X50 (โปรตอน เอ็กซ์50) กำลังถูกพูดถึงอย่างมากในมาเลเซีย ด้วยความเพียบพร้อมทั้งคุณภาพตัวรถ
MG V801.ภายใน MG V80 กว้างขวางจุดเด่น MG V80 ก็คือด้านความกว้างขวาง เนื่องจากตัวถังที่ค่อนข้างใหญ่ ถ้าเทียบกับคู่แข่งก็จะเห็นว่าความกว้างความยาวความสูงล้วนแต่มากกว่าแทบทุกจุด2
2021 MG EP (เอ็มจี อีพี) เปิดตัวโฉมไมเนอร์เชนจ์ในประเทศจีน ขายแล้วในชื่อ Roewe ei5 เปลี่ยนหน้าตาครั้งใหญ่
2020 MG HS PHEV (เอ็มจี เอชเอส พีเอชอีวี) เปิดตัวอย่างเป็นทางการด้วยราคาที่เรียกเสียงฮือในงานแถลงข่าวที่
หลังจาก 2020 MG Gloster (เอ็มจี กลอสเตอร์) ได้รับการเผยโฉมรุ่นต้นแบบโปรโตไทพ์ในอินเดียไปตั้งแต่เดือนกุมภาพันธ์ที่ผ่านมา
2020 MG ZS EV ในเมืองไทย2021 MG ZS EV (2021 เอ็มจี แซดเอส อีวี) รถพลังงานไฟฟ้าโฉมใหม่จ่อเปิดตัวในประเทศไทย
รถต้นแบบ MG E-Motionรถสปอร์ตพลังงานไฟฟ้ารุ่นแรกของ MG (เอ็มจี) ยุคใหม่เตรียมเปิดตัวครั้งแรกในโลกภายในช่วงปลายปีนี้
2021 MG EP (2021 เอ็มจี อีพี) รถแวกอนเปิดตัวอย่างเป็นทางการด้วยราคา 988,000 บาท ส่วนทางด้าน MG ZS EV
2021 MG EPNew 2021 MG EP (2021 เอ็มจี อีพี) เปิดตัวอย่างเป็นทางการแล้ว มาพร้อมระบบขับเคลื่อนพลังงานไฟฟ้าชาร์จเต็มหนึ่งครั้งวิ่งได้ไกลประมาณ
MG (เอ็มจี) แบรนด์รถยนต์น้องใหม่ประเทศไทย ประกาศขึ้นแท่นผู้นำตลาดเอสยูวีในครึ่งแรกของปี 2563 ด้วยยอดจำหน่ายรวม
MG (เอ็มจี) ได้รับรางวัลแบรนด์รถยนต์ที่ความคุ้มค่ายอดเยี่ยม (Best Value Brand 2020) จากการประกาศผลรางวัล
MG Motor ค่ายรถยนต์ที่กำลังมาแรงในขณะนี้ กำลังขยับขยายการผลิตด้วยการเพิ่มโมเดลรถยนต์ไฟฟ้าที่ราคาจับต้องได้
MG (เอ็มจี) ผู้นำด้านรถยนต์ไฟฟ้าในประเทศไทย ประกาศเดินหน้าแผนงานขยายสถานีประจุไฟฟ้า 500 แห่งทั่วประเทศ
MG ZS EV รถอเนกประสงค์พลังงานไฟฟ้าล้วน ที่ออกแบบเพื่อตอบโจทย์การใช้ชีวิตสไตล์คนเมือง ด้วยความจุแบตเตอรี่
2021 MG Marvel R (2021 เอ็มจี มาร์เวล อาร์) รถเอสยูวีไฟฟ้ารุ่นใหม่เตรียมเปิดตัวออกสู่ตลาดยุโรปเป็นแห่งแรก
MG V80 (เอ็มจี วี80)เป็นรถตู้โดยสารขนาด 11 ที่นั่งของค่าย MG ที่มีจุดเด่นในการวางเครื่องยนต์ด้านหน้า
2020 Proton X50 (โปรตอน เอ็กซ์50) เปิดตัวอย่างเป็นทางการแล้วในประเทศมาเลเซีย พร้อมกับกระแสข่าวว่าคอรถยนต์ชาวไทยจะได้ใช้กันแน่นอนภายในอีก
ว่า MG5 (เอ็มจี5) ใหม่อาจจะเข้ามาในไทย หรือที่ฮือฮากันใน Facebook ที่มีการปล่อยภาพโทรศัพท์พร้อมตรา MG
และต้องบอกเลยว่า MG กล้าหาญชาญชัยมากที่นำรถกระบะ MG EXTENDER (เอ็มจี เอกซ์เทนเดอร์) เข้ามาขายในประเทศไทย
2021 MP EPสิ่งหนึ่งที่มีความแน่นอนสำหรับผู้ที่สนใจและอยากได้รถยนต์ไฟฟ้า คือ นับจากนี้ไป ราคาจำหน่ายจะลดลงไปแปรผกผันกับความแพร่หลายในตัวเลือกที่จะมากขึ้น
ความสำเร็จของรถอเนกประสงค์ค่าย MG ทั้ง MG ZS (เอ็มจี แซดเอส) และ MG HS (เอ็มจี เอชเอส) แสดงให้เห็นว่าค่ายรถยนต์น้องใหม่สามารถโค่นแบรนด์ยักษ์อันเก่าแก่ลงได้หากเดินถูกทางยอดขายสะสมของรถอเนกประสงค์ขนาดซับคอมแพ็กต์อย่าง
MG Extender 2.0 Giant Cab D 6MT ราคา 619,000 บาท- MG Extender 2.0 Giant Cab GRAND D 6MT ราคา 659,000
MG (เอ็มจี) ประเทศไทย ขยับสายการผลิตเพิ่มการผลิต MG ZS (เอ็มจี แซดเอส) พวงมาลัยซ้าย เพื่อเริ่มการส่งออกไปยังตลาดเวียดนามภายในสิ้นปีนี้
MG HS (เอ็มจี เอชเอส) ถือเป็นรถอเนกประสงค์อีกรุ่นที่ได้รับความนิยมไม่แพ้ MG ZS ของค่ายเอ็มจีเลย ด้วยความโดดเด่นในด้านเทคโนโลยี
หลังจาก MG HS รถสไตล์รถครอบครัวจากแบรนด์จีนเปิดตัวก็ได้รับความสนใจล้นหลาม และก็กลายเป็น Compact SUV ที่มียอดขายดีในกลุ่มได้อย่างรวดเร็วด้วยชื่อ
แล้วตู้ชาร์จไฟในศูนย์การเรียนรู้แห่งนี้ถือว่าหลากหลายและมีความพร้อมมากที่สุดแห่งหนึ่ง โดยมีตู้ที่ผมเห็น 3 ตู้ ปล่อยกระแสไฟ 90, 50
2020 MG ZS (เอ็มจี แซดเอส) รถเอสยูวีโฉมใหม่ได้รับรองมาตรฐานความปลอดภัยระดับ 5 ดาวจาก Asean NCAP แต่คะแนนการทดสอบยังด้อยกว่า
เอ็มจี บริษัทรถยนต์ลูกครึ่งอังกฤษ-จีน นำเสนอ 2019 เอ็มจี เอชเอส (2019 MG HS) รถอเนกประสงค์เอสยูวีออกทำตลาดประเทศไทยทั้งหมด
MG (เอ็มจี) ลอนดอน ได้ทำการเปิดคอนเซปท์รถสปอร์ตคันใหม่ในนาม MG Cyberster แบบเปิดประทุน ก่อนที่จะมีรายละเอียดออกมาในงาน
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Sir mor lora jonor ALL ( Acute Lymphoblastic Leukemia a type of cancer) r maintenance chemotherapy soli ase, jar babe 6 MP tablet 50 mg khubei proyojon hoi ase. Sir anugraha kori mor lora jonor babe tablet tur bebostha kori diboloi apunak binomro anurodh jonaisu.
@ChouhanShivraj, @BhindCollector @SadhviPragya_MP @CMMadhyaPradesh सर मेरे पापा (senior citizen) मिहोना भिण्ड में रहते है उनको कुछ दवाइयां चाहिये जो की वहा नहीं मिल रही है जिनका नाम "Glizid-M Tablet" और "Losar 50 MG" मै अभी दिल्ली एनसीआर में हूँ कृपया करके सहयता करे
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Eighth manifestation of Dasmahavidyas or Ten Grand Wisdom Conferring Divine Mothers is called Baglamukhi. Bagla word is a deviation from the original Sanskrit word Valga meaning briddle. So this Divine Mother is, from the literal meaning, a Mother briddling the enemies. Hence this form of Grand Wisdom conferring Divine Mother is known as the dispeller of enemies. Baglamukhi originated as a result of the prayer of Devtas to God Vishnu when a demon named Madan had appeared as a storm in sea and challenged the former. So Baglamukhi is a shakti or essence of Lord Vishnu and thus also called as Pitambra or clad in yellow attire. Though she has a form of Shiva Mratiunjwshwar as her Bhairav. ( Image source: google) Baglamukhi sadhana is instant result giving forms of worship. Immediately She blesses the devotee with boon if pleased or with punishment if sadhana is not done properly. Like a current of electricity the devotee shall feel her influence in experience. Consequently, this is one of the most sought after Divine Mothers these days especially by the politicians, or those embroiled in legal and family troubles. However, this form of Divine Mother should not be invoked for frivolous purposes. You will get what you want but will have to bear a karmic cost. It is like 50 mg tablet which will instantly give you the relief from the fever but to have so powerful a drug at your own without the prescription of a doctor ( guru in this case) will have side effects of more fatal nature. Sadhana of Dasmahavidya including Baglamukhi has a systematic and specilised method. First it has to be initiated by a guru. Second, some innocently ignorant people and pundits start doing its sadhana with the thirty six lettered mantra. It is so powerful that devotee becomes enthusiastic and also greedy. But this mantra is the pinnacle of sadhana like syllabus of PhD. If a nursery class student is reading the PHD syllabus, he will not only fail but also destroy the development of his brain. Similarly, to have so much high pitch energy without being physically and mentally ready will have dire consequences like aggression, disorientation etc. Single letter mantra is a like a seed and the thirty six letter mantra told on TV channels by some astrologers is a fully developed tree. You will rip your self apart trying to embrace the tree without a proper seed being sowed by an adept master at the right time. Baglamukhi sadhana begins with guru giving the single lettered beej mantra first. This has to be recited in fixed number day cycles of pure and strict living called purshcharan for at least ten lakhs times to move to the second stage which is a four letter mantra. These pursharans are more effective on auspicious occassions like navratra, gupt navratra, festivals and eclipse period. But Divine Mother mantra recitation needs a protective environment so some mantras have to be chanted in order to have a protective cover at the place one is doing Sadhana. That is why it need guidance. In this way, the Divine Mother residing as Kundalini Shakti will become active. Then a ceremony called Shaktabhiskek is perfomed by Guru and the devotee is given new enhanced syllabus for sadhana. Turning Maa Bagla’s speciality towards our own internal enemies like misfortune, physical ailments, anger and greed and so many impurites blesses one with fastest spiritual growth as without these impurites being cleared, the divine cannot be experienced. With a genuine guru behind, the extraordinary energy of Maa Bagla will act as a ladder to growth and not as a cliff to fall. Why we use our powers is our own choice. Going this way Dasmahavidya is the shortest and surest way to realise our optimum power where Shakti as Kundalini power will merge into Shiva at the crown of head exactly the same way as a Yogi does it through meditation and a bhakt or devotee by the outpouring of love and compassion towards the names and forms of Hari. Rigveda says: Reality is one, however scholars call it by different names…Rigveda Note: With Her grace, I am a initiated shakt into Baglamukhi by a Kamakhya Tradition Master. Two famous Baglanukhi Temples: Pitambara Peeth at Datia MP Webpage of MP Goverment about more information. https://www.google.com/url?sa=t&source=web&rct=j&url=https://datia.nic.in/en/tourist-place/pitambara-peeth-datia/&ved=2ahUKEwjf-vLb9cjpAhWFzDgGHVh6C0AQFjALegQIBhAB&usg=AOvVaw19kPGB1lQ1TCIZD4-bFVuw&cshid=1590200420968 Baglamukhi Temple at Vankhandi( kangra) HP This is located on Chandigarh Kangra highway twenty kilometers behind Kangra at a place named Vankhandi.
Thanks for the a2a. No it isn't. This is an anabolic steroid called Stanozolol (Winstrol). There used to be a misconception that because it had weak anabolic and androgenic effect (making it useful only in a cutting phase, not for building mass), that it was less toxic. Unfortunately, the opposite seems to be true. Neurabol is just another brandname of stanozolol. The commonly known brand is Winstrol. Read about the negative effects in the article pasted below. HTH Update: Instead of pasting links, I’m pasting the entire article (including references) here. Credits go to Dan Gwartney, MD: Winstrol: Bad News and More Bad News Written by Dan Gwartney, MD Wednesday, 06 January 2010 In 1988, the sporting world was rocked by the announcement proclaiming that Ben Johnson, a Canadian sprinter who’d just shamed Carl Lewis in the Olympic 100-meter race, tested positive for anabolic steroid use. Johnson, who tested positive for stanozolol, was banned for several years from competition, losing his gold medal and an estimated $8.2 million in endorsements.1 Then, the Steroid Control Act of 1990 was passed and steroids became classified as a controlled substance. Little Potency, Lots of Danger Stanozolol, known classically by the trade name Winstrol, is a relatively mild steroid in terms of mass or strength gains, yet is extremely popular, particularly with bodybuilders and performance athletes.2 Winstrol (now sold under a variety of brand names and varying tablet strengths and concentrations) was originally available either as a low-strength tablet of two milligrams or as an aqueous suspension containing 50 milligrams per milliliter (mg/ml). Its use was commonly reserved for pre-competition phases for bodybuilders, as it aided in imparting a hardened appearance. In an audiotape series released in 1995 by the magazine Muscle Media 2000, one speaker suggested that a number of runners, particularly endurance runners, used a comparatively low dose of Winstrol to prevent muscle loss secondary to the catabolism experienced during long-distance training and competitions. Stanozolol is the generic name for the chemical 17-Methyl-5alpha-androstano(3,2-c)pyrazol-17beta-ol, identified as CAS registry number 302-96-5.3 Considered to be a highly anabolic steroid due to its impressive anabolic/androgenic ratio, it’s in fact a very mild steroid in terms of muscle or strength gains. The surprising lack of potency is explained by the fact that stanozolol is a very weak androgen and as an anabolic agent, is less effective than a comparable dose of testosterone.4 Despite its relatively low potency, stanozolol is still commonly abused, in part due to its reputation for being a “safe” steroid. While stanozolol does not have the more dramatic or obvious side effects seen with many of the highly androgenic steroids, it’s by no means safe. In fact, the published record of medical reports suggests stanozolol may be one of the most dangerous forms of steroids to use. State of Confusion The confusion surrounding stanozolol is understandable as its actions are complex and poorly understood. Stanozolol, based upon the highly androgenic, reduced form of testosterone, DHT, would seemingly be a potent androgen, responsible for increased aggression, hair loss and acne. In fact, stanozolol is a very weak androgen4 and rather than promoting aggression, it’s been found to suppress aggression in animals such that they will not even respond to physical provocation or the presence of a male intruder.5,6 Further, the male sex glands, specifically the seminal vesicles, do not respond to stanozolol as a testosterone substitute and rats maintained on stanozolol lose the ability to ejaculate,6,7 eventually eliminating all sexual behavior.8 A similar response is seen in female rats failing to become sexually receptive under the influence of estrogen.9 Thus, in terms of behavior, stanozolol appears to act more as an anti-androgen, rather than an androgen. If these results are applicable to humans, it would make an athlete less competitive and interfere with normal sexual relations. Complicating the social and psychological effects of stanozolol are the numerous reports demonstrating that stanozolol actively blocks normal brain function in a variety of receptor systems, and may interfere with anti-depressants and anxiety medications.10-12 Many steroid users describe a period of “depression” after completing a cycle of steroids and the findings from these studies suggest stanozolol may be exceptionally problematic for those who are subject to the psychological effects of steroid withdrawal. While stanozolol may be a less likely candidate to cause events described as “roid rage,” it may be a dangerous drug for anyone predisposed to suicide or other psychological trauma. Examined by Science Referring back to its chemical structure, as a DHT derivative, stanozolol is a reduced steroid, meaning it’s not a substrate for the enzyme aromatase, which is the enzyme responsible for converting most androgens into estrogens (female hormones). Indeed, few bodybuilders report estrogen-related side effects during or following a stanozolol-only cycle. However, the safety of stanozolol in this regard appears to be overstated; drawing upon an animal study, stanozolol was found to accelerate sexual maturation in female, pre-pubescent mice.13 This effect was prevented when an estrogen blocker was given to the mice prior to the stanozolol treatment. Interestingly, though stanozolol caused early changes in the vaginas of these mice, it was not strong enough at the dose studied to cause complete sexual maturation. While this study is inconclusive, it might suggest that stanozolol may be capable of acting as a partial-agonist for the estrogen receptor, similar to the more familiar Nolvadex (Tamoxifen). Though it may not be a substrate for aromatase, meaning it is resistant to being converted into an estrogenic (female) hormone, stanozolol can modestly stimulate aromatase activity, possibly adding to the potential for other androgens to be converted to estrogens.14 Another study, examining the effects of stanozolol on skin cells in a lab, discovered that some of the results produced by stanozolol were unique, not explained by its chemical relationship to testosterone.15 Stanozolol has been shown to increase collagen production,16 as well as certain prostaglandins and enzymes within the skin. Investigating this phenomenon, researchers discovered that in the skin fibroblast (an early, undeveloped skin cell), stanozolol could not be displaced (removed) by nortestosterone (an androgen), dexamethasone (a cortisol derivative) or estradiol (an estrogen). Rather, it was partially displaced by progesterone, another female hormone.15 Again, it was interesting to note that though progesterone could displace stanozolol from receptors in the skin cells, progesterone failed to cause the same response. The actions of stanozolol are unclear from this study. It may be possible that stanozolol is capable of interacting with many different receptors, either interfering with other hormones or acting as a weak substitute. None of these studies directly implicate stanozolol as an estrogenic or feminizing compound, and most users’ experiences with stanozolol would confirm that it is non-estrogenic, leading to a hardened appearance with minimal water retention and few reports of gynecomastia. However, the effect of stanozolol, when combined with other agents, may not be as worry free. Liver Toxicity Stanozolol is provided in both oral and injectable forms. The chemical is identical in both preparations, the practical difference being that the injectable suspension allows for a higher concentration, usually at a lower cost.2 Stanozolol may be taken orally due to the presence of a methyl group (a small side chain) added to the steroid structure. This addition of the methyl group makes stanozolol one of the 17-alkylated steroids, which are commonly known for being more toxic to the liver than the injectable steroid esters. The liver toxicity of stanozolol is often understated, with most users believing stanozolol is among the least toxic of steroids. In fact, the exact opposite may be closer to the truth. Oral stanozolol has been used for many years in the treatment of a variety of medical conditions, and new uses are being investigated.17-28 Even under conditions in which the drug is prescribed by a physician, dispensed from a legitimate pharmacy, and taken as directed, serious liver damage can occur. In some of the long-term studies reported, half or more of the subjects needed to have the dose lowered or even discontinue treatment due to elevations of the liver enzymes, a sign of cellular damage.22,26 However, most studies concluded that in nearly all cases, the signs and symptoms of liver damage went away with proper intervention and that stanozolol was felt to be a safe treatment alternative for certain conditions.18-20,22,25,27,28 The damaging effect of stanozolol upon the liver appears to be very common, and is of greater severity at higher doses. A binding protein has been discovered in rat and human liver specific for stanozolol and danazol, another steroid.29 Studies have proven stanozolol to be hepatotoxic (damaging to the liver).30-32 The effect of an extremely high level of stanozolol (400 times the recommended dose) upon liver cells failed to show any evidence of stanozolol causing or promoting cancer in those cells, even when exposed to other known carcinogens.33 This does not mean, however, that stanozolol is protective against cancer or risk-free, as these results would have to be confirmed and other chemicals may interact with stanozolol in a way that was not evaluated. A case report has been published detailing severe liver damage and acute renal failure in a bodybuilder following the use of stanozolol (i.m. 50 mg every other day) stacked with metandienone (10-50 mg/day) for 80 days.34 This 28-year-old man showed up jaundiced (yellow skin and eyes) three weeks after completing his cycle, and deteriorated for seven weeks until time and treatment allowed him to recover (at significant expense). More Bad News This is not the only reported case of serious health consequences associated with stanozolol. A brief literature search revealed two deaths due to heart attacks,35 two heart attack survivors,36,37 one dangerous cardiac rhythm38 and a life-threatening blood loss,39 all in young men. Few steroids are so commonly associated with serious events such as these, which suggests stanozolol is not yet fully understood. There are a number of other side effects and consequences associated with stanozolol use, but these are well known and generally accepted by the professional and athletic community. Briefly, stanozolol negatively affects the risk of heart attack or stroke by lowering the “good cholesterol” and raising the “bad cholesterol.”25,40,41 Women may experience masculinizing effects even at very low doses (2 mg/day).2,22,26,28 Stanozolol also increases the risk of serious bleeding, from the annoyance of nosebleeds to the life-threatening condition known as esophageal varices;23-25,31,39 may make tendons more prone to injury;42,43 is easily detected in hair and urine and remains detectable for several months following discontinuation;44-48 suppresses natural testosterone production;49,50 and dramatically lowers the carrier protein for androgens in the blood, called sex-hormone binding protein (SHBG).51,52 SHBG, which protects androgens from being metabolized and cleared from the body, is decreased by 50 percent with three days’ use of a low dose of stanozolol.51,52 At first glance, this may appear to be a positive effect, making what androgens are injected or swallowed less likely to be “bound” (prevented from stimulating muscle growth), instead allowing the steroid to float in the bloodstream as a “free” steroid, whereby it can interact with the muscle cell and cause hypertrophy. This is not such a benefit in the body, as SHBG protects androgens from rapid degradation and allows for the effect of testosterone or other androgens to persist for a longer period. SHBG lowers as a defense mechanism, allowing the body to shed excess androgens more quickly. Summing Up In conclusion, stanozolol, generally known as Winstrol, is a commonly abused steroid that’s felt by many users to be a very mild and safe anabolic. Though stanozolol doesn’t carry the risk of the more obvious and dramatic androgenic or estrogenic side effects of other drugs, it may be all the more dangerous for its subtle nature. Stanozolol appears to act upon many different systems in the body and brain, affecting many functions beyond androgen-stimulated hypertrophy of the muscle. It’d been shown to mimic the effects of estrogen and shares a binding site with progesterone (female hormones); decreases sexual drive, sexual function and aggression; may cause or interfere with the treatment of psychological disorders; is highly likely to cause liver damage (fortunately this appears to be reversible in most cases); and may be involved with the development of life-threatening or fatal events, including heart attacks and bleeding. It may cause the body to more rapidly clear androgens and is easily detectable for long periods in both hair and urine. Bodybuilders report using doses of 50-100 mg/day,2 yet doses as low as six to 10 mg/day have been shown to increase nitrogen retention greater than 200-300 milligrams of testosterone enanthate/week.53 This low dose has been used safely in studies monitored by physicians, though more than half of users, even at this low dose, need to have the dose lowered or discontinued due to liver damage or other side effects. Given that there are other steroids with fewer known risks, and that stanozolol is comparatively weak as both an androgen and an anabolic steroid, greater caution should be used by those considering stanozolol. References 1. Benjamin D. Shame of the Games. Available through Time Magazine online, http://www.time.com/time/daily/newsfiles/olympics/summer88/johnson.html accessed June 28, 2002. 2. Llewellyn W. Anabolics 2002. Molecular Nutrition Press, Patchogue NY, 2002 pp 177-80. 3. ChemIDPlus. Provided through the National Library of Medicine. Available at Chemical information with searchable synonyms, structures, and formulas accessed June 28, 2002. 4. Saartok T, Dahlberg E, et al. Relative binding affinity of anabolic-androgenic steroids: comparison of the binding to the androgen receptors in skeletal muscle and in prostate, as well as to sex hormone-binding globulin. Endocrinology 1984 Jun;114(6):2100-6. 5. McGinnis MY, Lumia AR, et al. Physical provocation potentiates aggression in male rats receiving anabolic androgenic steroids. Horm Behav 2002 Feb;41(1):101-10. 6. Clark AS, Barber DM. Anabolic-androgenic steroids and aggression in castrated male rats. Physiol Behav 1994 Nov;56(5):1107-13. 7. Clark AS, Harrold EV. Comparison of the effects of stanozolol, oxymetholone, and testosterone cypionate on the sexual behavior of castrated male rats. Behav Neurosci 1997 Dec;111(6):1368-74. 8. Clark AS, Harrold EV, et al. Anabolic-androgenic steroid effects on the sexual behavior of intact male rats. Horm Behav 1997 Feb;31(1):35-46. 9. Blasberg ME, Clark AS. Anabolic-androgenic steroid effects on sexual receptivity in ovariectomized rats. Horm Behav 1997 Dec;32(3):201-8. 10. Masonis AE, McCarthy MP. Direct interactions of the androgenic/anabolic steroids with the peripheral benzodiazepine receptor in rat brain: implications for the psychological and physiological manifestations of androgenic/anabolic steroid abuse. J Steroid Biochem Mol Biol 1996 Aug;58(5-6):551-5. 11. Masonis AE, McCarthy MP. Effects of the androgenic/anabolic steroid stanozolol on GABAA receptor function: GABA-stimulated 36Cl-influx and [35S] TBPS binding. J Pharmacol Exp Ther 1996 Oct;279(1):186-93. 12. Masonis AE, McCarthy MP. Direct effects of the anabolic/androgenic steroids, stanozolol and 17 alpha-methyltestosterone, on benzodiazepine binding to the gamma-aminobutyric acid(a) receptor. Neurosci Lett 1995 Apr 7;189(1):35-8. 13. Whitney AC, Clark AS. Effects of acute stanozolol treatment on puberty in female rats. Biol Reprod 2001 May;64(5):1460-5. 14. Roselli CE. The effect of anabolic-androgenic steroids on aromatase activity and androgen receptor binding in the rat preoptic area. Brain Res 1998 May 11;792(2):271-6. 15. Ellis AJ, Cawston TE, et al. The differential effects of stanozolol on human skin and synovial fibroblasts in vitro: DNA synthesis and receptor binding. Agents Actions 1994 Mar;41(1-2):37-43. 16. Falanga V, Greenberg AS, et al. Stimulation of collagen synthesis by the anabolic steroid stanozolol. J Invest Dermatol 1998 Dec;111(6):1193-7. 17. Revenga F, Aguilar C, et al. Cryofibrinogenaemia with a good response to stanozolol. Clin Exp Dermatol 2000 Nov;25(8):621-3. 18. Parsad D, Pandhi R, et al. Stanozolol in chronic urticaria. J Dermatol 2001 Jun;28(6):299-302. 19. Helfman T, Falanga V. Stanozolol as a novel therapeutic agent in dermatology. J Am Acad Dermatol 1995 Aug;33(2 Pt 1):254-8. 20. Daniel F, Rao DG, et al. A pilot study of stanozolol for advanced breast carcinoma. Cancer 1991 Jun 15;67(12):2966-8. 21. Cooper RG, Mitchell WS, et al. Fibrinolytic enhancement with stanozolol fails to improve symptoms and signs in patients with post-surgical back pain. Scand J Rheumatol 1991;20(6):414-8. 22. Sheffer AL, Fearon DT, et al. Hereditary angioedema: a decade of management with stanozolol. J Allergy Clin Immunol 1987 Dec;80(6):855-60. 23. Broekmans AW, Conard J, et al. Treatment of hereditary protein C deficiency with stanozolol. Thromb Haemost 1987 Feb 3;57(1):20-4. 24. Belch JJ, Madhok R, et al. The effect of increasing fibrinolysis in patients with rheumatoid arthritis: a double blind study of stanozolol. Q J Med 1986 Jan;58(225):19-27. 25. Kluft C, Preston FE, et al. Stanozolol-induced changes in fibrinolysis and coagulation in healthy adults. Thromb Haemost 1984 Apr 30;51(2):157-64. 26. Chesnut CH, Ivey JL, et al. Stanozolol in postmenopausal osteoporosis: therapeutic efficacy and possible mechanisms of action. Metabolism 1983 Jun;32(6):571-80. 27. Cicardi M, Bergamaschini L, et al. Morphologic evaluation of the liver in hereditary angioedema patients on long-term treatment with androgen derivatives. J Allergy Clin Immunol 1983 Sep;72(3):294-8. 28. Cicardi M, Bergamaschini L, et al. Long-term treatment of hereditary angioedema with attenuated androgens: a survey of a 13-year experience. J Allergy Clin Immunol 1991 Apr;87(4):768-73. 29. Luzardo OP, Machin RP, et al. Photoaffinity labeling identification of a specific binding protein for the anabolic steroids stanozolol and danazol: an oligomeric protein regulated by age, pituitary hormones, and ethyl estradiol. Endocrinology 2000 Sep;141(9):3377-87. 30. Boada LD, Zumbado M, et al. Evaluation of acute and chronic hepatotoxic effects exerted by anabolic-androgenic steroid stanozolol in adult male rats. Arch Toxicol 1999 Nov;73(8-9):465-72. 31. Harkin KR, Cowan LA, et al. Hepatotoxicity of stanozolol in cats. J Am Vet Med Assoc 2000 Sep 1;217(5):681-4. 32. Welder AA, Robertson JW, et al. Toxic effects of anabolic-androgenic steroids in primary rat hepatic cell cultures. J Pharmacol Toxicol Methods 1995 Aug;33(4):187-95. 33. Ghia M, Mereto E. Assay of stanozolol for tumor initiating and promoting activity in two rat liver foci bioassays. Cancer Lett 1992 Apr 30;63(3):203-9. 34. Habscheid W, Abele U, et al. Severe cholestasis with kidney failure from anabolic steroids in a bodybuilder. Dtsch Med Wochenschr 1999 Sep 10;124(36):1029-32. 35. Fineschi V, Baroldi G, et al. Anabolic steroid abuse and cardiac sudden death: a pathologic study. Arch Pathol Lab Med 2001 Feb;125(2):253-5. 36. Mewis C, Spyridopoulos I, et al. Manifestations of severe coronary heart diease after anabolic drug abuse. Clin Cardiol 1996 Feb;19(2):153-5. 37. Goldstein DR, Dobbs T, et al. Clenbuterol and anabolic steroids: a previously unreported cause of myocardial infarction with normal coronary angiograms. South Med J 1998 Aug;91(8):780-4. 38. Sullivan ML, Martinez CM, et al. Atrial fibrillation and steroids. J Emer Med 1999 Sep-Oct;17(5):851-7. 39. Winwood PJ, Robertson DA, et al. Bleeding oesophageal varices associated with anabolic steroid use in an athlete. Postgrad Med J 1990 Oct;66(780):864-5. 40. Thompson PD, Cullinane EM, et al. Contrasting effects of testosterone and stanozolol on serum lipoprotein levels. JAMA 1989 Feb 24;261(8):1165-8. 41. Bausserman LL, Saratelli AL, et al. Effects of short-term stanozolol administration on serum lipoproteins in hepatic lipase deficiency. Metabolism 1997 Sep;46(9):992-6. 42. Inhofe PD, Grana WA, et al. The effects of anabolic steroids on rat tendon. An ultrastructural, biomechanical, and biochemical analysis. Am J Sports Med 1995 Mar-Apr;23(2):227-32. 43. Miles JW, Grana WA, et al. The effect of anabolic steroids on the biomechanical and histological properties of rat tendon. J Bone Joint Surg Am 1992 Mar;74(3):411-22. 44. Cirimele V, Kintz P, et al. Testing of anabolic stanozolol in human hair by gas chromatography-negative ion chemical ionization mass spectrometry. J Chromatogr B Biomed Sci Appl 2000 Apr 14;740(2):265-71. 45. Schanzer W, Opfermann G, et al. Metabolism of stanozolol: identification and synthesis of urinary metabolites. J Steroid Biochem 1990 Jun;36(1-2)):153-74. 46. Choo HY, Kwon OS, et al. Quantitative determination of stanozolol and its metabolite in urine by gas chromatography/mass spectrometry. J Anal Toxicol 1990 Mar-Apr;14(2):109-12. 47. Schanzer W, Delahaut P, et al. Long-term detection and identification of metandienone and stanozolol abuse in athletes by gas chromatography-high-resolution mass spectrometry. J Chromatogr B Biomed Appl 1996 Dec 6;687(1):93-108. 48. Dumestre-Toulet V, Cirimele V, et al. Hair analysis of seven bodybuilders for anabolic steroids, ephedrine, and clenbuterol [In Process Citation] J Forensic Sci 2002 Jan;47(1):211-4. 49. Ballarin E, Guglielmini C, et al. Unmodified performance in runners following anabolic steroid administration. Int J Sports Med 1986 Dec;7(6):302-6. 50. Small M, Beastall GH, et al. Alteration of hormone levels in mormal males given the anabolic steroid stanozolol. Clin Endocrinol (Oxf) 1984 Jul;21(1):49-55. 51. Sinnecker GH, Hiort O, et al. Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene. German Collaborative Intersex Study Group. Eur J Pediatr 1997 Jan;156(1):7-14. 52. Sinnecker G, Kohler S. Sex hormone-binding globulin response to the anabolic steroid stanozolol: evidence for its suitability as a biological androgen sensitivity test. J Clin Endocrinol Metab 1989 Jun;68(6):1195-200. 53. Fryburg DA, Weltman A, et al. Short-term modulation of the androgen milieu alters pulsatile, but not exercise- or growth hormone (GH)-releasing hormone-stimulated GH secretion in healthy men: impact of gonadal steroid and GH secretory changes on metabolic outcomes. J Clin Endocrinol Metab 1997 Nov;82(11):3710-9.
Anaemia Normal Hb range- The normal ranges for hemoglobin depend on the age and, beginning in adolescence, the gender of the person. The normal ranges are: • Newborns: 17 to 22 gm/dL • One (1) week of age: 15 to 20 gm/dL • One (1) month of age: 11 to 15gm/dL • Children: 11 to 13 gm/dL • Adult males: 14 to 18 gm/dL • Adult women: 12 to 16 gm/dL • Men after middle age: 12.4 to 14.9 gm/dL • Women after middle age: 11.7 to 13.8 gm/dL PS. LEGEND SAYS----Black grapes, dried under the SUN, absorb divine energy and shrink. Dried raisins possess latent energy to be released by overnight soaking under water. If taken as stipulated, bone morrow & spleen are activated to produce new RBC. Time tested + highly effective measures:- Anemia*/Anaemia*Iron deficiency in blood-How to detect? The causes of anemia may be classified as impaired red blood cell (RBC) production, increased RBC destruction (hemolytic anemias), blood loss, and fluid overload (hypervolemia). Several of these may interplay to cause anemia. The most common cause of anemia is blood loss, but this usually does not cause any lasting symptoms unless a relatively impaired RBC production develops, in turn, most commonly by iron deficiency.  Just open up the lower eyelid and observe the color. Dark red reveals normal Hb levels. White/Pale red color reveals anemia. To prove it further a simple Hb test or CBP/CBC test is sufficient. 1. Anaemia— (Lack or poverty of blood/iron deficiency in blood); Anaemia of a destructive type is called pernicious anemia—CF 3x alone; if it fails mixture of CF 3x, CP 3x or 12x, FP 12x KM 3x, KP 3x, KS 3x, MP 3x, MM 3x and NP 3x failing which add NS 3x and S 12x. This is wonderful. This cures even pernicious anemia. To increase red corpuscles in blood give NM 3x. Take one tomato in the morning and one in the evening. China 30 thrice daily or Zinc Met 30 twice daily often cures. Mr. M. Hitaishi, the cashier of Allahabad University reports that his wife had been suffering from anemia for one year, she used to become unconscious and remain so for 2 or 3 days. He had given her the best Allopathic treatment, but it did no good. His neighbor Dr. Raizada, Lecturer in the University gave this mixture and within half an hour, she became conscious and never became unconscious again and her pain in the body disappeared at once. 2. Anemia— Spasms and pain caused by anemia—CP 3x. Dosage*: 2 grains t.d.s. • All these biochemical salts/Homeo medicines available @ local Homoeo shops are safe and with side benefits. Don’t swallow medicine. The medicine to be dissolved on/under the tongue. Don’t take anything 10 minutes before and 10 minutes after medication. You can take water. 3. • Deficiency of Blood (Anaemia) Nutrilage Plus & 1 Cap in the morning & evening. Neruri XT & 1 Cap twice a day after meals. Triphala Tab & 2 Caps twice a day after meals. Hb Xtrong & 1 capsule after lunch and dinner. • Patented Ayurveda Food & Nutrition Supplements manufactured in India and USA, approved by USFDA, KOSHER, HALAL, GMP, ISO, ETC., and made available at Stores in your vicinity in 40 countries all over the globe. No Side Effects. 4. a. Aloe Vera Juice [30 ml + 1 tsp of honey t.i.d.] b. Wheat Grass Powder: 1 cup of hot water + 1 tsp of honey + 1 tsp of WG powder morning and evening. c. 1. Treatment for increasing hemoglobin: Take black dried raisins as may be required daily. Soak them in half a cup of water overnight. Eat these black raisins as mentioned below and drink the water. Morning Afternoon Evening Day 1 1 1 1 Day 2 2 2 2 Day 3 3 3 3 Day 4 4 4 4 Day 5 4 4 4 Day 6 4 4 4 Day 7 3 3 3 Day 8 2 2 2 Day 9 1 1 1 2. Check the hemoglobin level of the blood. If necessary, repeat as above after 8/10 days and continue in the same way, till the hemoglobin level is satisfactory. This treatment may also be given to all the patients of cancer, T. B., paralysis, arthritis, and brain problem or having a chronic problem and also to the children who have a deficiency of hemoglobin. 3. Check if the parents have a deficiency of haemo¬globin and if so ask them to take treatment. 4. Take Iron rod weighing 60 gms. from a local foundry. Put it 8 glasses of plain water. Boil it until reduced to 2 glasses. Take it hot, hot by storing in a thermos flask throughout the day for 10 days. Iron-rich foods: There are two variants of iron - non-heme and heme iron. For instance, chicken, eggs, and meat are the most reliable sources of heme iron which is well-absorbed by the body and can support good health. Plant-based iron-rich foods contain non-heme iron, but they are not absorbed easily by the body. If you are a vegetarian, then you should take adequate amounts of Vitamin C while taking cereals, bread, fruits, and vegetables. Foods that improve hemoglobin: Consume iron-rich food products: According to the National Anaemia Action Council, lack of iron is the most common cause behind low hemoglobin levels. To improve iron content in your blood, you can take asparagus, tofu, almonds, oysters, fortified breakfast cereals, liver, red meat, shrimp, spinach, dates, and lentils. However, consult your doctor for the right intake, as too much consumption of iron may be harmful to your health. Improve your vitamin C intake: Absorption of iron is improved if vitamin C is taken in adequate quantities. Lemon, tomatoes, papaya, oranges, strawberries, bell peppers, broccoli, grapefruit, etc. are some of the fruits that are rich in vitamin C. In fact, if there is a deficiency of vitamin C in our blood, hemoglobin levels go down. You may also take vitamin supplements to improve hemoglobin in your body, but consult a doctor first. Focus on food items rich in folic acid: This acid is basically a vitamin B complex, which is required to make red blood cells. Food products that are rich in folic acid include rice, liver, breakfast cereals, sprouts, dried beans, wheat germ, peanuts, etc. A diet comprising 200-400 milligrams of foliates is enough to supplement your Vitamin B needs. Include beetroot as a part of your diet: Rich in iron, folic acid, fibers and potassium, beetroot helps in augmenting hemoglobin levels. Drinking beetroot juice daily increases the iron content in your red blood cells. Have apples: They are rich in iron and if you have an apple daily, then your hemoglobin level will improve significantly. If possible, take a green apple with its skin. Apple juice mixed with beetroot juice has a marked effect on hemoglobin levels. You can also add some ginger or lemon juice to this mixture and have the concoction twice a day. Eat blackstrap molasses: This food is rich in iron, vitamin, folic acid, etc and improves the hemoglobin level in your blood. Take 2 tablespoons of blackstrap molasses and apple cider vinegar each, mix them in a cup of water and drink this concoction once a day. Diet Restrictions: Here are some foods you should avoid with your pro-anemia diet: 1-Beware of Tannins: These naturally occurring substances are found in many plant-based foods, and interfere with the absorption of iron from non-heme (a form of iron found in plants and fortified foods) sources, particularly leafy, vegetable sources. Representative food sources include grapes, and black, green, and rooibos tea. However, these teas need not be avoided entirely. You must simply switch consumption from meal times to between meals. Also, they do not inhibit iron absorption in heme (a form of iron found in meat, poultry, and seafood) sources. 2-Limit your Coffee and Alcohol: Not only do the tannins in coffee and wine inhibit iron absorption, but taking any of these drinks in excess also greatly inhibits folate absorption, which is also necessary for manufacturing new red blood cells. However, you can still take coffee at least 1 hour before or after a meal, as it only affects absorption when consumed simultaneously with iron and folate foods. 3-Watch the Gluten: Those suffering from celiac disease are unable to absorb the protein gluten, which in turn damages the intestinal wall. Celiac disease is also a major cause of anemia, which is why people with both celiac disease and anemia should avoid gluten-containing foods at all costs. Some examples of foods rich in the protein include wheat, barley, rye, oats, and foods that are made of or contain gluten; even in trace amounts. 4-Be Phytate Aware: Phytates and phytic acid are antioxidant compounds found in foods that are high in fiber. They bind with iron when ingested together with iron-containing items, rendering them unusable by the body. In fact, as little as 5-10 mg of phytates can interfere with the absorption of iron by 50%. However, soaking phytate-containing foods before cooking can help remove or reduce their iron-binding properties. Some of the most popular phytate foods include white and brown rice, white flour, whole-grain wheat, legumes, and nuts. 5-Avoid Calcium with Iron: Dairy products like milk, cheese, and yogurt are high in calcium, may be necessary for good bone-strength, but can be detrimental to someone with anemia. This is because calcium limits the amount of iron that can be absorbed by the body, particularly when consumed alongside iron. However, calcium foods are necessary for overall health, and should, therefore, be consumed at different times of the day separately from iron-rich foods. Other food sources of calcium include beef, fish, beans, and calcium-fortified bread. 6-Avoid Soy: Along with being high in calcium, this popular alternative health food also contains phytic acid, and a protein-like molecule exclusive to soy. All three of these factors make soy highly dangerous for someone with anemia, and should, therefore, be avoided entirely. However, like tannin, soy, and soy food products only affect the absorption of non-heme iron obtained from plant and vegetable sources. Following are the traditional uses of honey, according to ayurveda: 1. Prevents anemia: Honey contains high amounts of iron, manganese and copper which are very essential for building haemoglobin. According to ancient texts, honey is a traditional cure as well as prevention for anemia as it helps in maintaining the optimum level of red blood corpuscles and haemoglobin. 2. Promotes eye health: Honey has been used to treat various eye diseases since ancient times. It is known to improve vision with daily application. It is an effective cure against diseases like conjunctivitis, trachoma or even something as minor as eye itching. It is also beneficial to treat glaucoma in the early stages. 3. Skin care: Ancient texts on ayurveda mention that external application of honey is effective in curing sores or other wounds. It works like an antiseptic and helps to soothe pain and hastens the healing process. It is also used to treat skin burns or carbuncles. 4. Cure for coughs: Honey is extremely useful in treating coughs. It works as a demulcent which aids in soothing the swollen mucous membrane present on the upper respiratory tract. It relieves you from irritating coughs and associated symptoms like frequent spurts of cough while talking and difficulty in swallowing. It is a chief ingredient in ayurvedic cough syrups for the same reason. You can also try honey gargles to relieve pain from throat inflammation.