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7. [Hereditary hepatic hyperbilirubinemias]. Vest M Ergeb Inn Med Kinderheilkd; 1969; 28():1-53. PubMed ID: 4896115 [No Abstract] [Full Text] [Related]
15. [Differential diagnosis of jaundice]. Heinrich K; Heinrich G Med Klin; 1966 Oct; 61(41):1630-4. PubMed ID: 5919990 [No Abstract] [Full Text] [Related]
17. The jaundiced patient. Axon AT Br J Hosp Med; 1979 May; 21(5):464-77. PubMed ID: 486831 [TBL] [Abstract][Full Text] [Related]
18. VPS33B mutation with ichthyosis, cholestasis, and renal dysfunction but without arthrogryposis: incomplete ARC syndrome phenotype. Bull LN; Mahmoodi V; Baker AJ; Jones R; Strautnieks SS; Thompson RJ; Knisely AS J Pediatr; 2006 Feb; 148(2):269-71. PubMed ID: 16492441 [TBL] [Abstract][Full Text] [Related]
19. Neonatal cholestasis, hyperferritinemia, hypoglycemia and deafness: a diagnostic challenge. van Westering-Kroon E; Heijligers M; Hütten MC BMJ Case Rep; 2019 Dec; 12(11):. PubMed ID: 31791989 [TBL] [Abstract][Full Text] [Related]
20. Pathogenic classification of jaundice. Orellana-Alcalde JM Rev Int Hepatol; 1968; 18(1):75-82. PubMed ID: 5678585 [No Abstract] [Full Text] [Related] [Next] [New Search]