Results 151 to 160 of about 1,143,701 (190)

Educational Case: Glucose-6-phosphate dehydrogenase (G6PD) deficiency anemia. [PDF]

Acad Pathol
Bussing K, Brehl N, Inman A, Davidson D.
europepmc   +1 more source

From bilirubin to breakthroughs: Contemporary outcomes in pediatric liver transplantation for cystic fibrosis. [PDF]

J Pediatr Gastroenterol Nutr
Leung DH.
europepmc   +1 more source

UGT1A1 genotype testing for irinotecan: A guideline developed by the UK Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI-PGx). [PDF]

Br J Clin Pharmacol
Chauhan D, Dello Russo C, Thompson J, Hughes DA, Payne K, Tsakiroglou M, Ross P, Chauhan R, Jenkinson S, Keen J, Harding S, Lau E, Braun M, Agarwal R, Adams R, Rolf E, Al-Sheikhli F, Mitchell S, Hammond R, Roberts R, Cairns L, Heggarty S, Graham J, Mencel J, Pirmohamed M.   +24 more
europepmc   +1 more source

Hepatic Safety of Orforglipron in Adults With Obesity or Overweight and/or Type 2 Diabetes: A Pooled Analysis of the Orforglipron Phase 3 Clinical Trials. [PDF]

Diabetes Obes Metab
Wharton S, Stefanski A, Chen J, Rao G, Twum EA, Denning M.   +5 more
europepmc   +1 more source

Gilbert's syndrome is not associated with HELLP syndrome

BJOG: An International Journal of Obstetrics & Gynaecology, 2001
The HELLP syndrome has been associated with postpartum unconjugated hyperbilirubinaemia. Several types of disorders cause unconjugated hyperbilirubinaemia, Gilbert's syndrome being the most common. In Caucasians a genetic defect in the TATA box of the promotor region of the gene encoding for bilirubin UDP‐glucuronyltransferase is tightly associated ...
Zusterzeel, P L, te Morsche, R, Raijmakers, M, Peters, W H, Steegers, E A   +4 more
openaire   +5 more sources

Neonatal hyperbilirubinemia and Gilbert's syndrome

Journal of Perinatal Medicine, 2002
The role of Gilbert's syndrome (GS) in neonatal hyperbilirubinemia, characterized by bilirubin levels higher than 223 microMol/L during the first seven days of life, has been investigated, evaluating the frequency of GS genotype (A(TA)7TAA polymorphism in the promoter of the gene encoding UGT1).
LAFORGIA N, FAIENZA MF, RINALDI A, D'AMATO G, RINALDI G, IOLASCON, ACHILLE   +5 more
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Gilbert syndrome

Orvosi Hetilap, 2008
Az ismert familiáris, nem konjugált hyperbilirubinaemiák közé tartozó Gilbert-szindróma az átlagpopuláció 7–10%-át érintő benignus kórkép. Tünetei rendszerint aspecifikusak, egyedül az esetlegesen előforduló sárgaság, továbbá az enyhén emelkedett nem konjugált bilirubin szintje utal a rendellenességre.
Bernadett, Faragó, Béla, Melegh
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Gilbert’s syndrome revisited

Journal of Hepatology, 2023
Gilbert's syndrome, also known as benign hyperbilirubinaemia, was described more than 100 years ago. It has usually been considered a physiological abnormality characterised by a mild elevation of the systemic level of unconjugated bilirubin, in the absence of any underlying liver or overt haemolytic disease.
Libor Vítek, Claudio Tiribelli
openaire   +2 more sources

Gilbert's syndrome

BMJ, 2011
A 22 year old man presents with a resolving episode of mild jaundice after an influenza-like illness. He reports a previous episode after an appendicectomy, which also resolved spontaneously, but he is worried about the implications of this recurrence. Biochemical records from his surgical admission show a slightly raised bilirubin concentration of 48 ...
Lee C, Claridge, Matthew J, Armstrong, Caroline, Booth, Paramjit S, Gill   +3 more
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Gilbert's syndrome

Baillière's Clinical Gastroenterology, 1989
While Gilbert's syndrome is extremely common and benign, its pathogenesis may not be as straightforward as once believed. It has been used as a model to examine aberrations of virtually every step in bilirubin metabolism. The clinical hallmarks are of a hereditary, chronic, mild unconjugated hyperbilirubinaemia.
K J, Watson, J L, Gollan
openaire   +2 more sources