Results 101 to 110 of about 1,401 (195)

POPULATION STUDIES ΟΝ UNCONJUGATED HYPERBILIRUBINAEMIA - GILBERT'S SYNDROME

, 2015
Σκοπός της εργασίας ήταν η μελέτη της συχνότητας της εμφάνισης του συνδρόμου Gilbert στου πληθυσμό μιας αγροτικής κοινότητας. Εξετάσθηκε η χολερυθρίνη του ορού σε 283 άτομα, ηλικίας 5-87 ετών, αφού κατατάχθηκαν σε τρεις ομάδες.
ΜΑΛΤΕΖΟΣ, Ε., ΠΑΠΑΪΩΑΚΕΙΜ, Μ., ΓΚΟΤΣΗΣ, Ν., ΡΑΖΗΣ-ΑΛΕΞΑΝΔΡΑΤΟΣ, Ν., ΚΑΜΠΟΥΡΟΜΥΤΗ, Γ., ΑΝΤΩΝΙΑΔΗΣ, Α.   +5 more
core  

A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome. [PDF]

Intern Med, 2023
Nato Y, Kageyama Y, Suzuki K, Shimojima Yamamoto K, Kanno H, Miyashita H.   +5 more
europepmc   +1 more source

A case of congenital dyserythropoietic anemia type II, Gilbert's syndrome and malleolar trophic ulcers

, 2002
A case of a woman with congenital dyserythropoietic anemia type II (CDA-II), Gilbert's syndrome (GS) and trophic malleolar ulceration is described.
BORDI B, BORDI E, GUARIGLIA R, ROSARIA D'AMICO M, CAPOBIANCO G, TIRELLI, Armando   +5 more
core   +1 more source

Serum free fatty acids and bilirubin concentration during fasting in patients with Gilbert's syndrome and normal controls

, 1987
The increments in serum concentrations of unconjugated bilirubin and free fatty acids (FFA) were measured 24 and 48 h after reduction of the caloric intake (400 cal/day) in 17 patients with Gilbert's syndrome (GS) and in 12 healthy control subjects.
Baldini, G, Orzes, N, Mangiarotti, Ma, Sottocasa, Gl, Tamaro, G, Parco, S, Lunazzi, Gc, TIRIBELLI, CLAUDIO   +7 more
core  

Bilirubin, platelet activation and heart disease: A missing link to cardiovascular protection in Gilbert's syndrome?

, 2015
Gilbert's syndrome (GS) is a relatively common condition, inducing a benign, non-hemolytic, unconjugated hyperbilirubinemia. Gilbert's Syndrome is associated with mutation in the Uridine Glucuronosyl Transferase 1A1 (UGT1A1) gene promoter, reducing ...
Kundur, Avinash R, Bulmer, Andrew C, Singh, Indu, Bulmer, Andrew, Kundur, Avinash   +4 more
core   +1 more source

(TA)(8) allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome

, 1999
BACKGROUND AND OBJECTIVE: Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinemia, is caused by a reduction in the activity of hepatic bilirubin UDP-glucuronosyltransferase (UGT1A1).
Centra, M, Savoia, A, Storelli, S, Faienza, MF, Iolascon, A, Zelante, L   +5 more
core   +1 more source

[Gilbert's syndrome: hyperbilirubinemia enemy or friend]. [PDF]

Zhonghua Gan Zang Bing Za Zhi, 2021
Xiang GQ, Sun FR, Wang BY.
europepmc   +1 more source

A Case of Gilbert’s Syndrome

, 1970
A middle aged lady presented with recurrent jaundice with normal SGPT, serum alkaline phosphatase, serum albumin and prothrombin time. Haemolysis was excluded by normal haemoglobin, peripheral blood film and reticulocyte count and finally she was ...
A Wazib, JK Saha, SS Hossain, SB Shahid, MZ Hossain, KA Al-Mamun   +5 more
core   +1 more source

Gilbert's Syndrome, Bilirubin Level and UGT1A1∗28 Genotype in Men of North-West Region of Russia. [PDF]

J Clin Exp Hepatol, 2021
Ivanov A, Semenova E.
europepmc   +1 more source

An Unusual Presentation of Gilbert Syndrome

ACG Case Reports Journal
ABSTRACT Unconjugated hyperbilirubinemia arises from elevated bilirubin production, impaired hepatic uptake, or reduced bilirubin conjugation, the latter often attributed to hereditary factors such as Gilbert syndrome involving mutations in the diphosphoglucuronate-glucuronosyltransferase 1A1 gene.
Chilakala, Akhila, Davis, Brenton G., Goldman, Max, Mukhtar, Nizar A.   +3 more
openaire   +2 more sources