Results 271 to 280 of about 57,539 (299)

The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

New England Journal of Medicine, 1995
Jayanta Roy Chowdhury, Dick Lindhout, Guido N J Tytgat   +2 more
exaly  

Idiopathic Unconjugated Hyperbilirubinemia (Gilbert's Syndrome)

New England Journal of Medicine, 1967
Barbara H Billing
exaly  

Gilbert's disease.

Bulletin of the New York Academy of Medicine, 2000
openaire   +1 more source

Mice with hyperbilirubinemia due to Gilbert’s syndrome polymorphism are resistant to hepatic steatosis by decreased serine 73 phosphorylation of PPARα

American Journal of Physiology - Endocrinology and Metabolism, 2017
Terry D Hinds, Peter A Hosick, Shujuan Chen   +2 more
exaly  

Gamma Glutamyl Transferase Activity in Gilbert's Disease

Endoscopy, 2006
RA Raja Ali, FM Stevens, H Grimes
openaire   +1 more source

Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases

Clinica Chimica Acta, 2016
Manu Jamwal, Anu Aggarwal, Man Updesh Singh Sachdeva   +2 more
exaly  

[Observations on Gilbert-Behçet disease].

Bericht uber die Zusammenkunft. Deutsche Ophthalmologische Gesellschaft, 1966
J, Wollensak, W, Frenger
openaire   +1 more source

[Familial case of Gilbert's disease].

Nihon rinsho. Japanese journal of clinical medicine, 1967
S, Takamatsu, H, Hiraga, T, Soejima, K, Nagamura, T, Yonetani   +4 more
openaire   +1 more source

Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome)

Bailliere's Best Practice and Research in Clinical Gastroenterology, 2010
Christian P Strassburg
exaly  

Decreased oxidation susceptibility of plasma low density lipoproteins in patients with Gilbert's syndrome

Journal of Gastroenterology and Hepatology (Australia), 2008
Muhittin A Serdar, Kemal Dağalp
exaly