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27. [Treatment of various forms of icterus or cholestasis with phenobarbital (author's transl)]. Stiehl A Z Gastroenterol; 1977 Jun; 15(6):404-16. PubMed ID: 888491 [TBL] [Abstract][Full Text] [Related]
32. [The first case of Crigler-Najjar syndrome in the Czech Republic]. Vítek L; Bosma P; de Boer A; Jirsa M; Brodanová M; Kotal P Cas Lek Cesk; 1996 Feb; 135(4):114-6. PubMed ID: 8625381 [TBL] [Abstract][Full Text] [Related]
33. [Comparison of three methods evaluating the saturation of serum bilirubin transporters in children with type I Crigler Najjar disease]. Francoual J; Myara A; Trivin F; Leluc R; Odièvre M Arch Fr Pediatr; 1990 Dec; 47(10):721-3. PubMed ID: 2082845 [TBL] [Abstract][Full Text] [Related]
34. Gilbert-Meulengracht's syndrome and pharmacogenetics: is jaundice just the tip of the iceberg? Strassburg CP Drug Metab Rev; 2010 Feb; 42(1):168-81. PubMed ID: 20070246 [TBL] [Abstract][Full Text] [Related]
35. [Considerations on a case of congenital nonhemolytic familial jaundice of the Crigler-Najjar type]. SALVIOLI GP Clin Pediatr (Bologna); 1962 Sep; 44():588-99. PubMed ID: 13991245 [No Abstract] [Full Text] [Related]
36. Familial nonhemolytic unconjugated hyperbilirubinemia (Crigler Najjar syndrome) with kernicterus - report of a case in Zambian child. Gupta K; Chintu C East Afr Med J; 1982 Mar; 59(3):225-9. PubMed ID: 7140605 [No Abstract] [Full Text] [Related]
37. [Crigler-Najjar syndrome. Report of one case with a long term follow up]. Besa S; Calvo CI; Harris PR Rev Med Chil; 2014 Jan; 142(1):109-13. PubMed ID: 24861123 [TBL] [Abstract][Full Text] [Related]
38. [Meulengracht's disease]. Scheurlen M Dtsch Med Wochenschr; 1989 Nov; 114(45):1767. PubMed ID: 2806109 [No Abstract] [Full Text] [Related]
39. Concurrence of Robinow syndrome and Crigler-Najar syndrome in two offspring of first cousins. Nazer H; Gunasekaran TS; Sakati NA; Nyhan WL Am J Med Genet; 1990 Dec; 37(4):516-8. PubMed ID: 2260598 [TBL] [Abstract][Full Text] [Related]
40. Retrovirus-mediated expression of HUG Br1 in Crigler-Najjar syndrome type I human fibroblasts and correction of the genetic defect in Gunn rat hepatocytes. Askari F; Hitomi E; Thiney M; Wilson JM Gene Ther; 1995 May; 2(3):203-8. PubMed ID: 7614251 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]