Search Results

Cholelithiasis in thalassemia major

Authors: Origa, Raffaella; Galanello, Renzo; Perseu, Lucia; Tavazzi, Dario; Domenica Cappellini, M.; Terenzani, Laura; Forni, Gian Luca; Quarta, Giovanni; Boetti, Tatiana; Piga, Antonio

Source: European Journal of Haematology, Volume 82, Number 1, January 2009 , pp. 22-25(4)

Publisher: Blackwell Publishing

Schizophrenia and Idiopathic Unconjugated Hyperbilirubinemia (Gilbert's Syndrome)

Authors: Miyaoka, Tsuyoshi; Wake, Rei; Hayashida, Maiko; Horiguchi, Jun

Source: Central Nervous System Agents in Medicinal Chemistry(Formerly Current Medicinal, Volume 8, Number 4, December 2008 , pp. 257-259(3)

Publisher: Bentham Science Publishers

Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosis

Authors: Amendola, Giovanni; Di Concilio, Rosanna; D'Urzo, Giovanna; Danise, Paolo; Parisi, Giuseppe; della Ragione, Fulvio; Rossi, Francesca; Nobili, Bruno; Perrotta, Silverio

Source: British Journal of Haematology, Volume 143, Number 4, November 2008 , pp. 593-595(3)

Publisher: Blackwell Publishing

Pharmacogenetics of Gilbert's syndrome

Author: Strassburg, Christian P

Source: Pharmacogenomics, Volume 9, Number 6, June 2008 , pp. 703-715(13)

Publisher: Future Medicine

Combined UGT1A1 and UGT1A7 variant alleles are associated with increased risk of Gilbert's syndrome in Taiwanese adults

Authors: Teng; Huang; Tang; Yang; Tseng

Source: Clinical Genetics, Volume 72, Number 4, October 2007 , pp. 321-328(8)

Publisher: Blackwell Publishing

Camptothecin and Podophyllotoxin Derivatives: Inhibitors of Topoisomerase I and II – Mechanisms of Action, Pharmacokinetics and Toxicity Profile

Authors: Hartmann, Jörg T.; Lipp, Hans-Peter

Source: Drug Safety, Volume 29, Number 3, 2006 , pp. 209-230(22)

Publisher: Adis International

Schizophrenia and Idiopathic Unconjugated Hyperbilirubinemia (Gilbert's Syndrome)

Authors: Miyaoka, Tsuyoshi; Horiguchi, Jun

Source: Current Psychiatry Reviews, Volume 1, Number 2, June 2005 , pp. 133-138(6)

Publisher: Bentham Science Publishers

Stimulation of transcriptional expression of human UDP-glucuronosyltransferase 1A1 by dexamethasone

Authors: Masanobu Kanou; Toru Usui; Hisao Ueyama; Hiroshi Sato; Iwao Ohkubo; Takaharu Mizutani

Source: Molecular Biology Reports, Volume 31, Number 3, September 2004 , pp. 151-158(8)

Publisher: Springer

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

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

Source: Colorectal Disease, Volume 6, Number 2, March 2004 , pp. 129-130(2)

Publisher: Blackwell Publishing

Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler–Najjar syndrome type I and Gilbert's syndrome

Authors: Maruo Y.; Poon K-H.; Ito M.; Iwai M.; Takahashi H.; Mori A.; Sato H.; Takeuchi Y.

Source: Clinical Genetics, Volume 64, Number 5, November 2003 , pp. 420-423(4)

Publisher: Blackwell Publishing

Elevated Bilirubin and Visual Perception in Pilots

Authors: Goerres, Hans-Peter; Weber, Frank

Source: Aviation, Space, and Environmental Medicine, Volume 74, Number 3, March 2003 , pp. 278-280(3)

Publisher: Aerospace Medical Association

Clinical features of schizophrenia associated with idiopathic unconjugated hyperbilirubinemia (Gilbert's Syndrome)

Authors: Tsuyoshi Miyaoka; Rei Yasukawa; Sohichi Mizuno; Tsuruhei Sukegawa; Takuji Inagaki; Jun Horiguchi

Source: International Journal of Psychiatry in Clinical Practice, Volume 7, Number 3, September 2003 , pp. 199-203(5)

Publisher: Informa Healthcare

Pharmacokinetics of morphine are not altered in subjects with Gilbert's syndrome

Authors: Skarke C.; Schmidt H.; Geisslinger G.; Darimont J.; Lötsch J.

Source: British Journal of Clinical Pharmacology, Volume 56, Number 2, August 2003 , pp. 228-231(4)

Publisher: Blackwell Publishing

Familial Neurofibromatosis-1 and Gilbert Syndrome

Authors: Kocer U.; Uysal A.; Sungur N.; Karaaslan O.; Kankaya Y.; Tiftikcioglu Y.

Source: Dermatologic Surgery, Volume 29, Number 7, July 2003 , pp. 759-765(7)

Publisher: Blackwell Publishing

A Case of Congenital Dyserythropoietic Anemia Type II, Gilbert's Syndrome and Malleolar Trophic Ulcers

Authors: Bordi, Bruno; Rosaria D'Amico, Maria; Guariglia, Roberto; Capobianco, Gaetana; Bordi, Emilio; Tirelli, Angelo

Source: Hematology, Volume 7, Number 3, January 2002 , pp. 197-199(3)

Publisher: Maney Publishing

Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome

Authors: Sutomo R.; Laosombat V.; Sadewa A.H.; Yokoyama N.; Nakamura H.; Matsuo M.; Nishio H.

Source: Pediatrics International, Volume 44, Number 4, August 2002 , pp. 427-432(6)

Publisher: Blackwell Publishing

Severe Jaundice in a Patient with a Previously Undescribed Glucose-6-phosphate Dehydrogenase (G6PD) Mutation and Gilbert Syndrome

Authors: Beutler E.; Gelbart T.; Miller W.

Source: Blood Cells, Molecules, and Diseases, Volume 28, Number 2, 2002 , pp. 104-107(4)

Publisher: Academic Press

Identification of a Defect in the UGT1A1 Gene Promoter and Its Association with Hyperbilirubinemia

Authors: Sugatani J.; Yamakawa K.; Yoshinari K.; Machida T.; Takagi H.; Mori M.; Kakizaki S.; Sueyoshi T.; Negishi M.; Miwa M.

Source: Biochemical and Biophysical Research Communications, Volume 292, Number 2, March 2002 , pp. 492-497(6)

Publisher: Academic Press

Role of UGT1A1 mutation in fasting hyperbilirubinemia

Authors: Ishihara, Tomoaki; Kaito, Masahiko; Takeuchi, Keisuke; Gabazza, Esteban C; Tanaka, Yuji; Higuchi, Kunihiro; Ikoma, Jiro; Watanabe, Shozo; Sato, Hiroshi; Adachi, Yukihiko

Source: Journal of Gastroenterology and Hepatology, Volume 16, Number 6, June 2001 , pp. 678-682(5)

Publisher: Blackwell Publishing

Pharmacogenetics: A Tool for Individualising Antineoplastic Therapy

Authors: Innocenti F.; Iyer L.; Ratain M.J.

Source: Clinical Pharmacokinetics, Volume 39, Number 5, November 2000 , pp. 315-325(11)

Publisher: Adis International