These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome. Aggarwal V; Seth A; Sharma S; Aneja S; Sammarco P; Fabiano C Pediatr Blood Cancer; 2010 Apr; 54(4):627-8. PubMed ID: 19953640 [TBL] [Abstract][Full Text] [Related]
7. Studies of glucuronidation in 3 infants with familial congenital nonhemolytic jaundice. HOLMAN GH; GOLUBOFF N J Pediatr; 1962 Aug; 61():303-4. PubMed ID: 13908495 [No Abstract] [Full Text] [Related]
8. Congenital familial nonhemolytic jaundice with kernicterus; a new clinical entity. CRIGLER JF; NAJJAR VA AMA Am J Dis Child; 1952 Feb; 83(2):259-60. PubMed ID: 14884759 [No Abstract] [Full Text] [Related]
9. [A FURTHER CASE OF CRIGLER-NAJJAR DISEASE]. LEVYMDE L; PORTELA R Rev Port Pediatr Pueric; 1965; 28():25-33. PubMed ID: 14293207 [No Abstract] [Full Text] [Related]
10. [A case with type I Crigler-Najjar syndrome]. Nong SH; Xie YM; Chen GR; Zhang BT Zhonghua Er Ke Za Zhi; 2003 May; 41(5):382. PubMed ID: 14751073 [No Abstract] [Full Text] [Related]
11. Prolonged neonatal jaundice: a manifestation of heterozygote state for Crigler--Najjar syndrome? Odièvre M; Luzeau R; Alagille D J Pediatr Gastroenterol Nutr; 1982; 1(2):239-41. PubMed ID: 6821110 [TBL] [Abstract][Full Text] [Related]
13. Beyond plasma bilirubin: the effects of phototherapy and albumin on brain bilirubin levels in Gunn rats. Cuperus FJ; Schreuder AB; van Imhoff DE; Vitek L; Vanikova J; Konickova R; Ahlfors CE; Hulzebos CV; Verkade HJ J Hepatol; 2013 Jan; 58(1):134-40. PubMed ID: 22922094 [TBL] [Abstract][Full Text] [Related]
14. [Clinical and diagnostic value of determining bile pigments]. Tsirkina AS Lab Delo; 1984; (9):569-71. PubMed ID: 6210416 [No Abstract] [Full Text] [Related]
15. Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes. Sampietro M; Iolascon A Haematologica; 1999 Feb; 84(2):150-7. PubMed ID: 10091414 [TBL] [Abstract][Full Text] [Related]
16. [Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases]. Aloulou H; Ben Thabet A; Khanfir S; Ben Mansour L; Chabchoub I; Labrune P; Kammoun T; Hachicha M Tunis Med; 2010 Oct; 88(10):707-9. PubMed ID: 20890816 [TBL] [Abstract][Full Text] [Related]
17. Management of Crigler-Najjar Syndrome type I. Al-Shurafa HA; Bassas AF; Broering DC; Rogiers XG; Wali SH; Burdelski MM Saudi Med J; 2001 Jun; 22(6):486-9. PubMed ID: 11426237 [TBL] [Abstract][Full Text] [Related]
18. Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome. Minucci A; Ruggiero A; Canu G; Maurizi P; De Bonis M; Concolino P; De Luca D; Capoluongo E Pediatr Blood Cancer; 2015 Sep; 62(9):1680-1. PubMed ID: 25822733 [No Abstract] [Full Text] [Related]
19. A CASE OF CRIGLER-NAJJAR'S DISEASE TREATED BY LIGHT IRRADIATION. SALAZARDESOUSA C Clin Pediatr (Bologna); 1964 Sep; 46():797-806. PubMed ID: 14266399 [No Abstract] [Full Text] [Related]