Works about GILBERT disease

Results: 65

The molecular basis of jaundice: An old symptom revisited.

Published in:

Liver International, 2017, v. 37, n. 8, p. 1094, doi. 10.1111/liv.13351

By:

Gazzin, Silvia;
Masutti, Flora;
Vitek, Libor;
Tiribelli, Claudio

Publication type:

Article

Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.

Published in:

Liver International, 2015, v. 35, n. 8, p. 2050, doi. 10.1111/liv.12785

By:

Shiu, Tzu ‐ Yue;
Huang, Hsin ‐ Hung;
Lin, Hsuan ‐ Hwai;
Shih, Yu ‐ Lueng;
Chu, Heng ‐ Cheng;
Chang, Wei ‐ Kuo;
Hsieh, Tsai ‐ Yuan

Publication type:

Article

Olfactory reference plus Truman symptoms in one patient with Gilbert syndrome and antiphospholipid antibodies (Hughes disease) secondary to probable chronic Lyme neuroborreliosis.

Published in:

2023

By:

Almeida e Melo, João;
Gama Marques, João

Publication type:

Letter

Mildly elevated unconjugated bilirubin is associated with reduced platelet activation-related thrombogenesis and inflammation in Gilbert’s syndrome.

Published in:

Platelets, 2017, v. 28, n. 8, p. 779, doi. 10.1080/09537104.2017.1280146

By:

Kundur, Avinash R.;
Santhakumar, Abishek B.;
Bulmer, Andrew C.;
Singh, Indu

Publication type:

Article

Unconjugated bilirubin inhibits collagen induced platelet activation.

Published in:

Platelets, 2014, v. 25, n. 1, p. 45, doi. 10.3109/09537104.2013.764405

By:

Kundur, Avinash R.;
Bulmer, Andrew C.;
Singh, Indu

Publication type:

Article

Unconjugated hyperbilirubinemia in a blood donor: Chance finding due to unusual plasma discoloration.

Published in:

Asian Journal of Transfusion Science, 2018, v. 12, n. 1, p. 8, doi. 10.4103/ajts.AJTS_34_17

By:

Jain, Ashish;
Khetan, Dheeraj

Publication type:

Article

Genetics of Drug-Induced Hepatotoxicity Toxicity in Gilbert's Syndrome.

Published in:

American Journal of Gastroenterology (Springer Nature), 2013, v. 108, n. 12, p. 1936, doi. 10.1038/ajg.2013.293

By:

Raza, Ali;
Vierling, John;
Hussain, Khozema B

Publication type:

Article

Painless obstructive jaundice leading to diagnosis of extrahepatic cholangiocarcinoma: a case study and review.

Published in:

Gastrointestinal Nursing, 2019, v. 17, p. S22, doi. 10.12968/gasn.2019.17.Sup10.S22

By:

Clark, Deborah

Publication type:

Article

Dynamic thiol/disulfide homeostasis and myeloperoxidase levels in Gilbert's syndrome with mild hyperbilirubinemia.

Published in:

Gastroenterology & Hepatology from Bed to Bench, 2024, v. 17, n. 3, p. 270, doi. 10.22037/ghfbb.v17i3.2968

By:

Furkan Demir, Burak;
Topcuoglu, Canan;
Turhan, Turan;
Altiparmak, Emin;
Yilmaz, Nisbet;
Ateç, ihsan

Publication type:

Article

Relationship between elevated bilirubin level and subclinical atherosclerosis as well as oxidative stress in Gilbert syndrome.

Published in:

Gastroenterology & Hepatology from Bed to Bench, 2020, v. 13, n. 2, p. 133

By:

Copur, Busra;
Yilmaz, Nisbet;
Topcuoglu, Canan;
Kiziltunc, Emrullah;
Cetin, Mustafa;
Turhan, Turan;
Demir, Burak Furkan;
Altiparmak, Emin;
Ates, Ihsan

Publication type:

Article

Frequency of the UGT1A1*28 Polymorphism in a Romanian Cohort of Gilbert Syndrome Individuals.

Published in:

Journal of Gastrointestinal & Liver Diseases, 2017, v. 26, n. 1, p. 25, doi. 10.15403/jgld.2014.1121.261.ugt

By:

Radoi, Viorica E.;
Ursu, Radu I.;
Poenaru, Elena;
Arsene, Cosmin;
Bohiltea, Camil L.;
Bohiltea, Roxana

Publication type:

Article

Atherosclerosis, lipids and lipoproteins.

Published in:: Clinical Chemistry & Laboratory Medicine, 2015, v. 53, p. s291, doi. 10.1515/cclm-2015-5006
Publication type:: Article

Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2014, v. 27, n. 8, p. 844, doi. 10.3109/14767058.2013.837879

By:

Žaja, Orjena;
Tiljak, Mirjana Kujundžić;
Štefanović, Mario;
Tumbri, Jasna;
Jurčić, Zvonko

Publication type:

Article

Perioperative Anesthetic Management of Patients Having Liver Transplantation for Uncommon Conditions.

Published in:

2018

By:

Bonavia, Anthony;
Pachuski, Justin;
Bezinover, Dmitri

Publication type:

journal article

The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome.

Published in:

Journal of Clinical & Diagnostic Research, 2016, v. 10, n. 11, p. 5, doi. 10.7860/JCDR/2016/19004.8810

By:

ALAEE, EHSAN;
BAZRAFSHAN, BEHNAZ;
AZAMINEJAD, ALI REZA;
FOULADINEJAD, MAHNAZ;
SHAHBAZI, MAJID

Publication type:

Article

Pregnancy with Gilbert Syndrome – A Case Report.

Published in:

2014

By:

MOHAN, MINI;
SAILAJA P., LAKSHMI;
NARASIMHA REDDY, PEDDIREDDY VIJAYA

Publication type:

Case Study

Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects.

Published in:

Journal of Clinical & Diagnostic Research, 2014, v. 8, n. 3, p. 63, doi. 10.7860/JCDR/2014/6674.4108

By:

ZAHEDPASHA, YADOLLAH;
AHMADPOUR, MOUSA;
NIAKI, HALEH AKHAVAN;
ALAEE, EHSAN

Publication type:

Article

Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.

Published in:

2018

By:

Gailite, Linda;
Rots, Dmitrijs;
Pukite, Ieva;
Cernevska, Gunta;
Kreile, Madara

Publication type:

journal article

Interleukin-2-induced reversible hyperbilirubinemia and cholestasis in a patient with Gilbert's syndrome.

Published in:

2002

By:

Engin, Hüseyin;
Oksüzoğlu, Cakmak Berna;
Altundağ, Kadri

Publication type:

Case Study

Gilbert's syndrome.

Published in:

2012

By:

Chandra, Alka;
Banavaliker, Jayant Nagesh;
Dixit, R. Madhubala

Publication type:

Case Study

Differentiating Gilbert Syndrome from Crigler Najjar Syndrome Type 2 by Phenobarbitone Test.

Published in:

Journal of Nepal Paediatric Society, 2015, v. 35, n. 1, p. 82, doi. 10.3126/jnps.v35i1.10620

By:

Sinha, R.;
Dalal, S.;
Sodhi, K.

Publication type:

Article

The Burden of Pathological Neonatal Jaundice and Its Determinants in Ethiopia: Systematic Review and Meta-Analysis.

Published in:

Journal of Neonatology, 2023, v. 37, n. 2, p. 108, doi. 10.1177/09732179231164520

By:

Tsehay, Binalfew;
Afework, Mekbeb

Publication type:

Article

Gilbert or Crigler–Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity.

Published in:

Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01251-4

By:

Cozzi, Laura;
Nuti, Federica;
Degrassi, Irene;
Civeriati, Daniela;
Paolella, Giulia;
Nebbia, Gabriella

Publication type:

Article

Do you really know what you get: the benefits and doubts of domino liver transplantation.

Published in:

Transplant International, 2018, v. 31, n. 11, p. 1198, doi. 10.1111/tri.13339

By:

Bechstein, Wolf O.;
Schnitzbauer, Andreas A.

Publication type:

Article

Gilbert syndrome in patients with type 1 diabetes-Prevalence, glycemic control, and microalbuminuria.

Published in:

Pediatric Diabetes, 2017, v. 18, n. 8, p. 803, doi. 10.1111/pedi.12488

By:

Singer, Sigal;
Pilpel, Nurit;
Pinhas‐Hamiel, Orit

Publication type:

Article

Accommodation Paralysis after Pheniramine Maleate Injection: A Case Report.

Published in:

Neuro-Ophthalmology, 2013, v. 37, n. 6, p. 257, doi. 10.3109/01658107.2013.830227

By:

Bingol Kiziltunc, Pinar;
Atilla, Huban;
Yalcindag, F. Nilufer

Publication type:

Article

Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome.

Published in:

2001

By:

Kaplan, Michael;
Hammerman, Cathy;
Beutler, Ernest;
Kaplan, M;
Hammerman, C;
Beutler, E

Publication type:

commentary

A case of anorexia nervosa with hyperbilirubinaemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene.

Published in:

1999

By:

Maruo, Y.;
Wada, S.;
Yamamoto, K.;
Sato, H.;
Yamano, T.;
Shimada, M.

Publication type:

journal article

Gilbert's syndrome: protective effect on endothelial dysfunction.

Published in:

Turkish Journal of Biochemistry / Turk Biyokimya Dergisi, 2016, v. 41, n. 6, p. 451, doi. 10.1515/tjb-2016-0150

By:

Sertoğlu, Erdim;
Tapan, Serkan;
Doğru, Teoman;
Acar, Ramazan;
Doğan, Tolga;
İnce, Selami;
Bilgi, Cumhur

Publication type:

Article

Pruritic and Painful Red Nodules and Papules.

Published in:: Clinical Infectious Diseases, 2017, v. 65, n. 11, p. 1952, doi. 10.1093/cid/cix580
Publication type:: Article

Low Left Ventricular Mass Index in Gilbert Syndrome? Arterial Stiffness Might Be the Missing Piece of the Puzzle.

Published in:

2023

By:

Şener, Yusuf Ziya

Publication type:

Letter to the Editor

Endothelial Dysfunction and Endocan Levels in Patients with Gilbert Syndrome and Moderate Hyperbilirubinemia.

Published in:

Angiology, 2022, v. 73, n. 10, p. 920, doi. 10.1177/00033197211057692

By:

Zengin, Oguzhan;
Sahiner, Enes Seyda;
Inan, Osman;
Topcuoglu, Canan;
Turhan, Turan;
Altiparmak, Emin;
Yilmaz, Nisbet;
Ates, Ihsan

Publication type:

Article

Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution.

Published in:

BioMed Research International, 2019, p. 1, doi. 10.1155/2019/6272174

By:

Mi, Xiao-xiao;
Yan, Jian;
Ma, Xiao-jie;
Zhu, Ge-li;
Gao, Yi-dan;
Yang, Wen-jun;
Kong, Xiao-wen;
Chen, Gong-ying;
Shi, Jun-ping;
Gong, Ling

Publication type:

Article

Nutrition in Gilbert's Syndrome—A Systematic Review of Clinical Trials According to the PRISMA Statement.

Published in:

Nutrients, 2024, v. 16, n. 14, p. 2247, doi. 10.3390/nu16142247

By:

Goluch, Zuzanna;
Wierzbicka-Rucińska, Aldona;
Książek, Ewelina

Publication type:

Article

High-colored plasma: a red signal for transfusion.

Published in:

2018

By:

Malhotra, Sheetal;
Negi, Gita;
Goyal, Bela;
Dhar, Minakshi

Publication type:

journal article

A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing.

Published in:

PLoS Computational Biology, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pcbi.1003825

By:

Chen, Yun-Ching;
Douville, Christopher;
Wang, Cheng;
Niknafs, Noushin;
Yeo, Grace;
Beleva-Guthrie, Violeta;
Carter, Hannah;
Stenson, Peter D.;
Cooper, David N.;
Li, Biao;
Mooney, Sean;
Karchin, Rachel

Publication type:

Article

Influence of Gilbert's syndrome on the formation of ethyl glucuronide.

Published in:

International Journal of Legal Medicine, 2015, v. 129, n. 5, p. 1005, doi. 10.1007/s00414-015-1157-7

By:

Huppertz, Laura;
Gunsilius, Leonie;
Lardi, Christelle;
Weinmann, Wolfgang;
Thierauf-Emberger, Annette

Publication type:

Article

Homozygous Mutation on the β -Globin Polyadenylation Signal in a Tunisian Patient with β -Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome.

Published in:

2017

By:

Haddad, Faten;
Trabelsi, Nawel;
Chaouch, Leila;
Darragi, Imen;
Oueslati, Meriem;
Boudriga, Imen;
Chaouachi, Dorra;
El-Borgi, Wijdene;
Hafsia, Raouf;
Abbes, Salem;
Ouragini, Houyem

Publication type:

Case Study

Serum Bilirubin Concentrations and the Prevalence of Gilbert Syndrome in Elite Athletes.

Published in:

Sports Medicine - Open, 2022, v. 8, n. 1, p. 1, doi. 10.1186/s40798-022-00463-6

By:

Woronyczová, Jana;
Nováková, Miroslava;
Leníček, Martin;
Bátovský, Miloš;
Bolek, Emil;
Cífková, Renata;
Vítek, Libor

Publication type:

Article

UGT1A1 gene linkage analysis: application of polymorphic markers rs4148326/rs4124874 in the Iranian population.

Published in:

Iranian Journal of Basic Medical Sciences, 2017, v. 20, n. 8, p. 880, doi. 10.22038/IJBMS.2017.9109

By:

Nadeali, Zakiye;
Vallian, Sadeq

Publication type:

Article

Prolonged Jaundice in a Premature Breastfed Infant With Gilbert's Syndrome.

Published in:

Journal of Human Lactation, 2024, v. 40, n. 2, p. 270, doi. 10.1177/08903344241227226

By:

Strobl, Frances;
Theurich, Melissa Ann

Publication type:

Article

Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India.

Published in:

Molecular Biology Reports, 2018, v. 45, n. 6, p. 2733, doi. 10.1007/s11033-018-4305-6

By:

Chiddarwar, Ashish S.;
D’Silva, Selma Z.;
Colah, Roshan B.;
Ghosh, Kanjaksha;
Mukherjee, Malay B.

Publication type:

Article

Hyperbilirubinemia following lenalidomide administration.

Published in:

2018

By:

Azmy, Veronica;
Neparidze, Natalia

Publication type:

Case Study

A familial Mediterranean fever girl due to MEFV N679H mutation with Gilbert's syndrome.

Published in:

2021

By:

Fujimaki, Yuki;
Soutome, Takehiko;
Tanaka, Takayuki;
Shiba, Takeshi;
Watanabe, Misa

Publication type:

Case Study

A Gilbert syndrome-associated haplotype protects against fatty liver disease in humanized transgenic mice.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65481-4

By:

Landerer, Steffen;
Kalthoff, Sandra;
Paulusch, Stefan;
Strassburg, Christian P.

Publication type:

Article

Gilbert's syndrome and fluorouracil toxicity in colorectal cancer patients: which correlation?

Published in:

2015

By:

Mandalà, M.;
Cremonesi, M.;
Cazzaniga, M.;
Rezzani, C.;
Ghilardi, M.;
Mary, C.;
Ferretti, G.;
Barni, S.

Publication type:

Letter to the Editor

GILBERT SYNDROME: A CASE SERIES.

Published in:

2017

By:

Mane, Sushant;
Ronghe, Ashwini

Publication type:

Case Study

UGT1A1 polymorphisms in cancer: impact on irinotecan treatment.

Published in:

Pharmacogenomics & Personalized Medicine, 2017, v. 10, p. 61, doi. 10.2147/PGPM.S108656

By:

Masashi Takano;
Toru Sugiyama

Publication type:

Article

Effect of hyperbilirubinaemia on neurocognitive, renal, bone and cardiovascular markers in HIV infection treated with boosted protease inhibitors.

Published in:

Journal of the International AIDS Society, 2014, v. 17, p. n/a, doi. 10.7448/IAS.17.4.19827

By:

Barber, Tristan J;
Moyle, Graeme;
Hill, Andrew;
Jagjit Singh, Gurmit;
Boffito, Marta;
Nelson, Mark

Publication type:

Article

The effect of zinc sulphate supplementation on atazanavir/ritonavir-associated hyperbilirubinemia.

Published in:

Journal of the International AIDS Society, 2012, v. 15, p. 1, doi. 10.7448/IAS.15.6.18305

By:

Jackson, A;
Else, L;
Back, D;
Yapa, M;
Seymour, N;
Ringner-Nackter, L;
Gazzard, B;
Boffito, M;
Moyle, G

Publication type:

Article