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Results 1 - 10 of 53 for Indian
  1. North American Indian childhood cirrhosis is a rare liver disorder that occurs in children. The liver malfunction causes yellowing of the ... it is treated with liver transplantation, North American Indian childhood cirrhosis typically causes life-threatening complications including ...
  2. ... gene has been found to cause North American Indian childhood cirrhosis, a chronic liver disease identified in ... Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification ...
  3. ... the Understanding of Autism Spectrum Disorder: Historical Perspective. Indian J Pediatr. 2017 Jan;84(1):44-52. ... Mukherjee SB. Autism Spectrum Disorders - Diagnosis and Management. Indian J Pediatr. 2017 Apr;84(4):307-314. ...
  4. ... studies in X-linked myotubular myopathy in three Indian families. Indian J Pediatr. 2010 Apr;77(4):431-3. ...
  5. ... Makitie O, Phadke SR. COL1A1 mutation in an Indian child with Caffey disease. Indian J Pediatr. 2011 Jul;78(7):877-9. ...
  6. ... Dowling-Degos Disease with Mottled Hypopigmentation in an Indian Family. Indian J Dermatol. 2014 Sep;59(5):476-80. ...
  7. ... Dowling-Degos Disease with Mottled Hypopigmentation in an Indian Family. Indian J Dermatol. 2014 Sep;59(5):476-80. ...
  8. ... as the Infallible Signature of Skin: An Overview. Indian J Dermatol. 2021 Nov-Dec;66(6):649- ...
  9. ... Shivananda, Christopher R, Kumar P. Type I hyperprolinemia. Indian J Pediatr. 2000 Jul;67(7):541-3. ...
  10. ... Familial exudative vitreoretinopathy (FEVR). Clinical profile and management. Indian J Ophthalmol. 2003 Dec;51(4):323-8. ...
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