ジルベール症候群 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ジルベール症候群" in Japanese language version.

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29nih.gov

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1hematologylibrary.org

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bmj.com

jmg.bmj.com

“Population studies on Gilbert's syndrome”. Journal of Medical Genetics: 152-156. (1975). doi:10.1136/jmg.12.2.152.

cnn.com

“Gilbert's syndrome”. Gilbert's (zheel-BAYRZ) syndrome typically is harmless and doesn't require treatment

dailymail.co.uk

Thornton, M. (2009年7月3日). “How our last Final hero, Henry 'Bunny' Austin, became an outcast for 40 years”. Daily Mail (London)

doi.org

“Gilbert症候群と血液疾患”. 日本小児血液学会雑誌. 6 18: 606. (2004年12月). doi:10.11412/jjph1987.18.6_601.
“Population studies on Gilbert's syndrome”. Journal of Medical Genetics: 152-156. (1975). doi:10.1136/jmg.12.2.152.
New insights in bilirubin metabolism and their clinical implications.. 19. (Oct 2013). p. 6401. doi:10.3748/wjg.v19.i38.6398. PMID 24151358.
Bancroft JD, Kreamer B, Gourley GR (1998). “Gilbert syndrome accelerates development of neonatal jaundice”. Journal of Pediatrics 132 (4): 656–60. doi:10.1016/S0022-3476(98)70356-7. PMID 9580766.
Cappellini MD, Di Montemuros FM, Sampietro M, Tavazzi D, Fiorelli G (1999). “The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels”. British journal of haematology 104 (4): 928–9. doi:10.1111/j.1365-2141.1999.1331a.x. PMID 10192462.
Marcuello E, Altés A, Menoyo A, Del Rio E, Gómez-Pardo M, Baiget M (2004). “UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer”. Br J Cancer 91 (4): 678–82. doi:10.1038/sj.bjc.6602042. PMC 2364770. PMID 15280927.
Rauchschwalbe S, Zuhlsdorf M, Wensing G, Kuhlmann J (2004). “Glucuronidation of acetaminophen is independent of UGT1A1 promotor genotype”. Int J Clin Pharmacol Ther 42 (2): 73–7. doi:10.5414/cpp42073. PMID 15180166.
Kohle C, Mohrle B, Munzel PA, Schwab M, Wernet D, Badary OA, Bock KW (2003). “Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians”. Biochem Pharmacol 65 (9): 1521–7. doi:10.1016/S0006-2952(03)00074-1. PMID 12732365.
Esteban A, Pérez-Mateo M (1999). “Heterogeneity of paracetamol metabolism in Gilbert's syndrome”. European journal of drug metabolism and pharmacokinetics 24 (1): 9–13. doi:10.1007/BF03190005. PMID 10412886.
Schwertner Harvey A; Vítek Libor (2008). “Gilbert syndrome, UGT1A1*28 allele, and cardiovascular disease risk: possible protective effects and therapeutic applications of bilirubin”. Atherosclerosis 198 (1): 1–11. doi:10.1016/j.atherosclerosis.2008.01.001. PMID 18343383.
Vítek L, Jirsa M, Brodanová M, and others (2002). “Gilbert syndrome and ischemic heart disease: a protective effect of elevated bilirubin levels”. Atherosclerosis 160 (2): 449–56. doi:10.1016/S0021-9150(01)00601-3. PMID 11849670.
Lin JP, O’Donnell CJ, Schwaiger JP, and others (2006). “Association between the UGT1A1*28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study”. Circulation 114 (14): 1476–81. doi:10.1161/CIRCULATIONAHA.106.633206. PMID 17000907.
Olsson R, Bliding A, Jagenburg R, Lapidus L, Larsson B, Svärdsudd K, Wittboldt S. (1988). “Gilbert's syndrome—does it exist? A study of the prevalence of symptoms in Gilbert's syndrome”. Acta Med Scandinavia 224 (5): 485–490. doi:10.1111/j.0954-6820.1988.tb19615.x. PMID 3264448.
Bailey A, Robinson D, Dawson AM. (1977). “Does Gilbert's disease exist?”. Lancet 1 (8018): 931–3. doi:10.1016/S0140-6736(77)92226-7. PMID 67389.
Larissa K. F. Temple, Robin S. McLeod, Steven Gallinger, James G. Wright (2001). “Defining Disease in the Genomics Era”. Science Magazine 293 (5531): 807–808. doi:10.1126/science.1062938. PMID 11486074.
Raijmakers MT, Jansen PL, Steegers EA, Peters WH (2000). “Association of human liver bilirubin UDP-glucuronyltransferase activity, most commonly due to a polymorphism in the promoter region of the UGT1A1 gene”. Journal of Hepatology 33 (3): 348–351. doi:10.1016/S0168-8278(00)80268-8. PMID 11019988.
Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN et al. (1995). “The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome”. New England Journal of Medicine 333 (18): 1171–5. doi:10.1056/NEJM199511023331802. PMID 7565971.
Monaghan G, Ryan M, Seddon R, Hume R, Burchell B (1996). “Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome”. Lancet 347 (9001): 578–81. doi:10.1016/S0140-6736(96)91273-8. PMID 8596320.
J L Gollan, C Bateman, B H Billing (1976). “Effect of dietary composition on the unconjugated hyperbilirubinaemia of Gilbert's syndrome”. Gut 17 (5): 335–340. doi:10.1136/gut.17.5.335. PMC 1411132. PMID 1278716.
N Carulli, M Ponz de Leon, E Mauro, F Manenti, A Ferrari (1976). “Alteration of drug metabolism in Gilbert's syndrome”. Gut 17 (8): 581–587. doi:10.1136/gut.17.8.581. PMC 1411334. PMID 976795.

elsevier.com

linkinghub.elsevier.com

Vítek L, Jirsa M, Brodanová M, and others (2002). “Gilbert syndrome and ischemic heart disease: a protective effect of elevated bilirubin levels”. Atherosclerosis 160 (2): 449–56. doi:10.1016/S0021-9150(01)00601-3. PMID 11849670.

gilbertssyndrome.com

GilbertsSyndrome.com

google.co.jp

books.google.co.jp

Shmaefsky, Brian (2006). “5”. Biotechnology 101. Greenwood Publishing Group. pp. 175. ISBN 978-0-313-33528-0

hematologylibrary.org

bloodjournal.hematologylibrary.org

del Giudice EM, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A (October 1999). “Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis”. Blood 94 (7): 2259–62. PMID 10498597.

liverfoundation.org

“Gilbert Syndrome”. American liver foundation. 2016年6月19日閲覧。

mayoclinic.com

http://www.mayoclinic.com/health/gilberts-syndrome/DS00743

medscape.com

emedicine.medscape.com

Gilbert Syndrome - eMedicine

nhs.uk

http://www.nhs.uk/conditions/gilbertssyndrome/Pages/Introduction.aspx

nih.gov

pubmed.ncbi.nlm.nih.gov

New insights in bilirubin metabolism and their clinical implications.. 19. (Oct 2013). p. 6401. doi:10.3748/wjg.v19.i38.6398. PMID 24151358.
Bancroft JD, Kreamer B, Gourley GR (1998). “Gilbert syndrome accelerates development of neonatal jaundice”. Journal of Pediatrics 132 (4): 656–60. doi:10.1016/S0022-3476(98)70356-7. PMID 9580766.
Cappellini MD, Di Montemuros FM, Sampietro M, Tavazzi D, Fiorelli G (1999). “The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels”. British journal of haematology 104 (4): 928–9. doi:10.1111/j.1365-2141.1999.1331a.x. PMID 10192462.
Marcuello E, Altés A, Menoyo A, Del Rio E, Gómez-Pardo M, Baiget M (2004). “UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer”. Br J Cancer 91 (4): 678–82. doi:10.1038/sj.bjc.6602042. PMC 2364770. PMID 15280927.
Rauchschwalbe S, Zuhlsdorf M, Wensing G, Kuhlmann J (2004). “Glucuronidation of acetaminophen is independent of UGT1A1 promotor genotype”. Int J Clin Pharmacol Ther 42 (2): 73–7. doi:10.5414/cpp42073. PMID 15180166.
Kohle C, Mohrle B, Munzel PA, Schwab M, Wernet D, Badary OA, Bock KW (2003). “Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians”. Biochem Pharmacol 65 (9): 1521–7. doi:10.1016/S0006-2952(03)00074-1. PMID 12732365.
Esteban A, Pérez-Mateo M (1999). “Heterogeneity of paracetamol metabolism in Gilbert's syndrome”. European journal of drug metabolism and pharmacokinetics 24 (1): 9–13. doi:10.1007/BF03190005. PMID 10412886.
Ladislav Novotnýc and Libor Vítek (2003). “Inverse Relationship Between Serum Bilirubin and Atherosclerosis in Men: A Meta-Analysis of Published Studies”. Experimental Biology and Medicine 228 (5): 568–571. PMID 12709588.
Schwertner Harvey A; Vítek Libor (2008). “Gilbert syndrome, UGT1A1*28 allele, and cardiovascular disease risk: possible protective effects and therapeutic applications of bilirubin”. Atherosclerosis 198 (1): 1–11. doi:10.1016/j.atherosclerosis.2008.01.001. PMID 18343383.
Vítek L, Jirsa M, Brodanová M, and others (2002). “Gilbert syndrome and ischemic heart disease: a protective effect of elevated bilirubin levels”. Atherosclerosis 160 (2): 449–56. doi:10.1016/S0021-9150(01)00601-3. PMID 11849670.
Lin JP, O’Donnell CJ, Schwaiger JP, and others (2006). “Association between the UGT1A1*28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study”. Circulation 114 (14): 1476–81. doi:10.1161/CIRCULATIONAHA.106.633206. PMID 17000907.
Olsson R, Bliding A, Jagenburg R, Lapidus L, Larsson B, Svärdsudd K, Wittboldt S. (1988). “Gilbert's syndrome—does it exist? A study of the prevalence of symptoms in Gilbert's syndrome”. Acta Med Scandinavia 224 (5): 485–490. doi:10.1111/j.0954-6820.1988.tb19615.x. PMID 3264448.
Bailey A, Robinson D, Dawson AM. (1977). “Does Gilbert's disease exist?”. Lancet 1 (8018): 931–3. doi:10.1016/S0140-6736(77)92226-7. PMID 67389.
Larissa K. F. Temple, Robin S. McLeod, Steven Gallinger, James G. Wright (2001). “Defining Disease in the Genomics Era”. Science Magazine 293 (5531): 807–808. doi:10.1126/science.1062938. PMID 11486074.
del Giudice EM, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A (October 1999). “Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis”. Blood 94 (7): 2259–62. PMID 10498597.
Horsfall LJ, Nazareth I, Pereira SP, Petersen I. (2013 Oct;28). “Gilbert's syndrome and the risk of death: a population-based cohort study.”. Journal of Gastroenterology and Hepatology 28 (10): 1643–1647. PMID 23701650.
Raijmakers MT, Jansen PL, Steegers EA, Peters WH (2000). “Association of human liver bilirubin UDP-glucuronyltransferase activity, most commonly due to a polymorphism in the promoter region of the UGT1A1 gene”. Journal of Hepatology 33 (3): 348–351. doi:10.1016/S0168-8278(00)80268-8. PMID 11019988.
Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN et al. (1995). “The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome”. New England Journal of Medicine 333 (18): 1171–5. doi:10.1056/NEJM199511023331802. PMID 7565971.
Monaghan G, Ryan M, Seddon R, Hume R, Burchell B (1996). “Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome”. Lancet 347 (9001): 578–81. doi:10.1016/S0140-6736(96)91273-8. PMID 8596320.
J L Gollan, C Bateman, B H Billing (1976). “Effect of dietary composition on the unconjugated hyperbilirubinaemia of Gilbert's syndrome”. Gut 17 (5): 335–340. doi:10.1136/gut.17.5.335. PMC 1411132. PMID 1278716.
N Carulli, M Ponz de Leon, E Mauro, F Manenti, A Ferrari (1976). “Alteration of drug metabolism in Gilbert's syndrome”. Gut 17 (8): 581–587. doi:10.1136/gut.17.8.581. PMC 1411334. PMID 976795.
Foulk, WT; Butt, HR; Owen, CA, Jr; Whitcomb, FF, Jr; Mason, HL (1959). “Constitutional hepatic dysfunction (Gilbert's disease): its natural history and related syndromes”. Medicine (Baltimore) 38 (1): 25–46. PMID 13632313.