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Results 1 - 10 of 17 for aria syndrome
  1. Crigler-Najjar syndrome 
    Crigler-Najjar syndrome is a very rare inherited disorder in which bilirubin cannot be broken down. Bilirubin is a substance made by the liver.
    https://medlineplus.gov/ency/article/001127.htm - Medical Encyclopedia
  2. SALL4 gene 
    ... 2006 Jan 3. Citation on PubMed Paradisi I, Arias S. IVIC syndrome is caused by a c.2607delA mutation in ...
    https://medlineplus.gov/genetics/gene/sall4 - Genetics
  3. Rotor syndrome 
    ... PubMed Central Wolkoff AW, Wolpert E, Pascasio FN, Arias IM. Rotor's syndrome. A distinct inheritable pathophysiologic entity. Am J Med. ...
    https://medlineplus.gov/genetics/condition/rotor-syndrome - Genetics
  4. Smith-Kingsmore syndrome 
    ... for Rare Disorders (NORD) ClinicalTrials.gov SMITH-KINGSMORE SYNDROME; SKS PubMed Gordo G, Tenorio J, Arias P, Santos-Simarro F, Garcia-Minaur S, Moreno ...
    https://medlineplus.gov/genetics/condition/smith-kingsmore-syndrome - Genetics
  5. Simpson-Golabi-Behmel syndrome 
    ... ajmg.a.31822. Citation on PubMed Tenorio J, Arias P, Martinez-Glez V, Santos F, Garcia-Minaur S, Nevado J, Lapunzina P. Simpson-Golabi-Behmel syndrome types I and II. Orphanet J Rare Dis. ...
    https://medlineplus.gov/.../condition/simpson-golabi-behmel-syndrome - Genetics
  6. Dubin-Johnson syndrome 
    ... 2012 Oct 12. Citation on PubMed Erlinger S, Arias IM, Dhumeaux ... Neonatal Dubin-Johnson syndrome: long-term follow-up and MRP2 mutations study. ...
    https://medlineplus.gov/genetics/condition/dubin-johnson-syndrome - Genetics
  7. MTOR gene 
    ... MTOR NCBI Gene ClinVar ... V, Lapunzina P. mTOR mutations in Smith-Kingsmore syndrome: Four additional patients and a review. Clin Genet. ...
    https://medlineplus.gov/genetics/gene/mtor - Genetics
  8. Golimumab Injection 
    Simponi® Aria ... or could not be tolerated. Golimumab injection (Simponi Aria) is also used to relieve the symptoms of ... vision, speech, and bladder control) or Guillain Barre syndrome (weakness, tingling, and possible paralysis due to sudden ...
    https://medlineplus.gov/druginfo/meds/a610010.html - Drugs and Supplements
  9. ATP1A3 gene 
    ... the variant causes the specific features of CAPOS syndrome. AT1A3_HUMAN ATPase, ... Blanco-Arias P, Einholm AP, Mamsa H, Concheiro C, Gutierrez- ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics
  10. Premenstrual Syndrome (PMS) (Department of Health and Human Services, Office on Women's Health)  
    Premenstrual Syndrome/Start Here ... Premenstrual Syndrome ... Department of Health and Human Services, Office on Women's Health
    https://www.womenshealth.gov/menstrual-cycle/premenstrual-syndrome - External Health Links
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