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Results 1 - 10 of 48 for Pathophysiology
  1. OPA1 gene 
    ... G, Reynier P. OPA1-associated disorders: phenotypes and pathophysiology. Int J Biochem Cell Biol. 2009 Oct;41( ... Diversity of clinical expression, modes of inheritance and pathophysiology. Neurobiol Dis. 2016 Jun;90:20-6. doi: ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  2. EPOR gene 
    ... Hodges VM, Rainey S, Lappin TR, Maxwell AP. Pathophysiology of anemia and erythrocytosis. Crit Rev Oncol Hematol. ...
    https://medlineplus.gov/genetics/gene/epor - Genetics
  3. SLC25A13 gene 
    ... Jalil MA, Begum L, Li MX. Pathogenesis and pathophysiology of citrin (a mitochondrial aspartate glutamate carrier) deficiency. ...
    https://medlineplus.gov/genetics/gene/slc25a13 - Genetics
  4. SLC22A5 gene 
    ... 5030. Citation on PubMed Tein I. Carnitine transport: pathophysiology and metabolism of known molecular defects. J Inherit ...
    https://medlineplus.gov/genetics/gene/slc22a5 - Genetics
  5. HSD17B3 gene 
    ... JE, Wilson JD, Russel DW. Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency. J ...
    https://medlineplus.gov/genetics/gene/hsd17b3 - Genetics
  6. MITF gene 
    ... Jimbow K. Elucidation of Melanogenesis Cascade for Identifying Pathophysiology and Therapeutic Approach of Pigmentary Disorders and Melanoma. ...
    https://medlineplus.gov/genetics/gene/mitf - Genetics
  7. COL3A1 gene 
    ... Beridze N, Frishman WH. Vascular Ehlers-Danlos syndrome: pathophysiology, diagnosis, and prevention and treatment of its complications. ...
    https://medlineplus.gov/genetics/gene/col3a1 - Genetics
  8. NPC2 gene 
    ... SL, Patterson MC, Balch W, Liscum L. The pathophysiology and mechanisms of NP-C disease. Biochim Biophys ...
    https://medlineplus.gov/genetics/gene/npc2 - Genetics
  9. SCN9A gene 
    ... SD, Yang Y, Waxman SG. Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes. ...
    https://medlineplus.gov/genetics/gene/scn9a - Genetics
  10. SLC6A8 gene 
    ... X-linked creatine transporter deficiency: clinical aspects and pathophysiology. J Inherit Metab Dis. 2014 Sep;37(5): ...
    https://medlineplus.gov/genetics/gene/slc6a8 - Genetics
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