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Results 1 - 10 of 38 for AG 85
  1. Renal and urological disorders 
    ... Practice . 10th ed. Philadelphia, PA: Elsevier; 2023:chap 85. Gharavi AG, Landry DW. Approach to the patient with renal ...
    https://medlineplus.gov/ency/article/001265.htm - Medical Encyclopedia
  2. Complement component 2 deficiency 
    ... md.0000152371.22747.1e. Citation on PubMed Sjoholm AG, Jonsson G, Braconier JH, Sturfelt G, Truedsson L. Complement deficiency and disease: an update. Mol Immunol. 2006 Jan;43(1-2):78-85. doi: 10.1016/j.molimm.2005.06.025. ...
    https://medlineplus.gov/.../complement-component-2-deficiency - Genetics
  3. Anabolic Steroids and Other Appearance and Performance Enhancing Drugs (APEDs) From the National Institutes of Health (National Institute on Drug Abuse)  
    Anabolic Steroids/Learn More ... Anabolic Steroids ... National Institute on Drug Abuse ... Anabolic steroids are synthetic variations of the male sex hormone testosterone. ...
    https://nida.nih.gov/research-topics/anabolic-steroids - External Health Links
  4. BSND gene 
    ... S, Fischer M, Ahmed ZM, Khan SY, Janssen AG, Zafar AU, Scholl U, Husnain T, Belyantseva IA, Friedman PL, Riazuddin S, Friedman TB, Fahlke C. Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. Am J Hum Genet. 2009 Aug;85(2):273-80. doi: 10.1016/j.ajhg. ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  5. Autosomal recessive congenital stationary night blindness 
    ... GA, Devery S, Moore AT, Holder GE, Robson AG, Webster AR. Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. Am J Hum Genet. 2009 Nov;85(5):711-9. doi: 10.1016/j.ajhg. ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
  6. TRPM1 gene 
    ... GA, Devery S, Moore AT, Holder GE, Robson AG, Webster AR. Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. Am J Hum Genet. 2009 Nov;85(5):711-9. doi: 10.1016/j.ajhg. ...
    https://medlineplus.gov/genetics/gene/trpm1 - Genetics
  7. Coffin-Lowry syndrome 
    ... J Pediatr Orthop. 2007 Jan-Feb;27(1):85-9. doi: 10.1097/01.bpo.0000187994.94515.9d. Citation on PubMed Hunter AG. Coffin-Lowry syndrome: a 20-year follow-up ...
    https://medlineplus.gov/genetics/condition/coffin-lowry-syndrome - Genetics
  8. EDNRB gene 
    ... 6273(03)00730-x. Citation on PubMed Baynash AG, Hosoda K, ... neurons. Cell. 1994 Dec 30;79(7):1277-85. doi: 10.1016/0092-8674(94)90018-3. ...
    https://medlineplus.gov/genetics/gene/ednrb - Genetics
  9. RET gene 
    ... cytogfr.2005.05.010. Citation on PubMed Baynash AG, Hosoda K, ... neurons. Cell. 1994 Dec 30;79(7):1277-85. doi: 10.1016/0092-8674(94)90018-3. ...
    https://medlineplus.gov/genetics/gene/ret - Genetics
  10. EDN3 gene 
    ... PubMed ENDOTHELIN 3; EDN3 ... for development of epidermal melanocytes and enteric neurons. Cell. 1994 Dec 30;79(7):1277-85. doi: 10.1016/0092-8674(94)90018-3. ...
    https://medlineplus.gov/genetics/gene/edn3 - Genetics
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