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22. [Gilbert's syndrome in patients with splenomegaly]. de Magalhães AF; Sevá-Pereira A Arq Gastroenterol; 1982; 19(4):187-9. PubMed ID: 7186402 [TBL] [Abstract][Full Text] [Related]
23. [Clinical Characteristics and Gene Mutations of Gilbert Syndrome Complicated with Myeloproliferative Neoplasm]. Li XX; Shi J; Huang ZD; Shao YQ; Nie N; Zhang J; Ge ML; Huang JB; Zheng YZ Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Apr; 25(2):567-571. PubMed ID: 28446312 [TBL] [Abstract][Full Text] [Related]
24. Gilbert syndrome and the development of antiretroviral therapy-associated hyperbilirubinemia. Rotger M; Taffe P; Bleiber G; Gunthard HF; Furrer H; Vernazza P; Drechsler H; Bernasconi E; Rickenbach M; Telenti A; J Infect Dis; 2005 Oct; 192(8):1381-6. PubMed ID: 16170755 [TBL] [Abstract][Full Text] [Related]
25. Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect. Yildiz D; Alan S; Kilic A; Yaman A; Erdeve O; Kuloglu Z; Atasay B; Arsan S Genet Couns; 2013; 24(3):273-7. PubMed ID: 24341141 [TBL] [Abstract][Full Text] [Related]
26. Intractable neonatal jaundice due to hereditary spherocytosis and Gilbert's syndrome. Ismail AQ; Gandhi A; El-Shimy N BMJ Case Rep; 2011 Jul; 2011():. PubMed ID: 22689841 [TBL] [Abstract][Full Text] [Related]
27. Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency. Kaplan M J Perinatol; 2001 Dec; 21 Suppl 1():S30-4; discussion S35-9. PubMed ID: 11803413 [TBL] [Abstract][Full Text] [Related]
28. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. Kadakol A; Ghosh SS; Sappal BS; Sharma G; Chowdhury JR; Chowdhury NR Hum Mutat; 2000 Oct; 16(4):297-306. PubMed ID: 11013440 [TBL] [Abstract][Full Text] [Related]
29. Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese. Akaba K; Kimura T; Sasaki A; Tanabe S; Wakabayashi T; Hiroi M; Yasumura S; Maki K; Aikawa S; Hayasaka K J Hum Genet; 1999; 44(1):22-5. PubMed ID: 9929972 [TBL] [Abstract][Full Text] [Related]
30. [Bromsulphalein clearance and hyperbilirubinemia in Gilbert's syndrome]. Cartei G; Chisesi T; Cazzavillian M; Barbui T; Battista R; Dini E Dtsch Z Verdau Stoffwechselkr; 1975; 35(4):169-73. PubMed ID: 1227811 [No Abstract] [Full Text] [Related]
31. Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening. Berrueco R; Alonso-Saladrigues A; Martorell-Sampol L; Català-Temprano A; Ruiz-Llobet A; Toll T; Torrebadell M; Naudó M; Camós M; Rives S Pediatr Blood Cancer; 2015 Jul; 62(7):1195-201. PubMed ID: 25855413 [TBL] [Abstract][Full Text] [Related]
32. [Inherited disorders of bilirubin metabolism]. Rossi F; Francese M; Iodice RM; Falcone E; Vetrella S; Punzo F; De Vita S; Perrotta S Minerva Pediatr; 2005 Apr; 57(2):53-63. PubMed ID: 15985997 [TBL] [Abstract][Full Text] [Related]