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  1. ... Other investigations chronic kidney disease in childhood with nephronophthisis; may have flank pain or haematuria with polycystic ... in PKD; retinitis pigmentosa in some forms of nephronophthisis; polydactyly in Bardet-Biedl syndrome urinalysis: usually acellular; ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
  2. ... Other investigations chronic kidney disease in childhood with nephronophthisis; may have flank pain or hematuria with polycystic ... in PKD; retinitis pigmentosa in some forms of nephronophthisis; polydactyly in Bardet-Biedl syndrome urinalysis: usually acellular; ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
  3. ... urinary tract obstruction. • Cerebral haemorrhage, stroke, and childhood nephronophthisis may be associated with cystic kidney disease. • Insulin ... Exa m chronic kidney disease in childhood with nephronophthisis; may have flank pain or haematuria with polycystic ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  4. ... urinary tract obstruction. • Cerebral hemorrhage, stroke, and childhood nephronophthisis may be associated with cystic kidney disease. • Insulin ... Exa m chronic kidney disease in childhood with nephronophthisis; may have flank pain or hematuria with polycystic ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  5. ... urinary tract obstruction. Cerebral haemorrhage, stroke, and childhood nephronophthisis may be associated with cystic kidney disease. Insulin ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  6. ... urinary tract obstruction. Cerebral hemorrhage, stroke, and childhood nephronophthisis may be associated with cystic kidney disease. Insulin ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  7. ... diagnosed until the later development of diabetes mellitus. Joubert syndrome: a rare condition usually inherited in an autosomal ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  8. ... 2018. All rights reserved. BASICS Retinitis pigmentosa Basics • Joubert syndrome: a rare condition usually inherited in an autosomal ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk