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579 results

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Page 1
A genetic study of Wilson's disease in the United Kingdom.
Coffey AJ, Durkie M, Hague S, McLay K, Emmerson J, Lo C, Klaffke S, Joyce CJ, Dhawan A, Hadzic N, Mieli-Vergani G, Kirk R, Elizabeth Allen K, Nicholl D, Wong S, Griffiths W, Smithson S, Giffin N, Taha A, Connolly S, Gillett GT, Tanner S, Bonham J, Sharrack B, Palotie A, Rattray M, Dalton A, Bandmann O. Coffey AJ, et al. Among authors: tanner s. Brain. 2013 May;136(Pt 5):1476-87. doi: 10.1093/brain/awt035. Epub 2013 Mar 21. Brain. 2013. PMID: 23518715 Free PMC article.
A study of Wilson disease mutations in Britain.
Curtis D, Durkie M, Balac (Morris) P, Sheard D, Goodeve A, Peake I, Quarrell O, Tanner S. Curtis D, et al. Among authors: tanner s. Hum Mutat. 1999;14(4):304-11. doi: 10.1002/(SICI)1098-1004(199910)14:4<304::AID-HUMU5>3.0.CO;2-W. Hum Mutat. 1999. PMID: 10502777
Wilson's Disease in Children: A Position Paper by the Hepatology Committee of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition.
Socha P, Janczyk W, Dhawan A, Baumann U, D'Antiga L, Tanner S, Iorio R, Vajro P, Houwen R, Fischler B, Dezsofi A, Hadzic N, Hierro L, Jahnel J, McLin V, Nobili V, Smets F, Verkade HJ, Debray D. Socha P, et al. Among authors: tanner s. J Pediatr Gastroenterol Nutr. 2018 Feb;66(2):334-344. doi: 10.1097/MPG.0000000000001787. J Pediatr Gastroenterol Nutr. 2018. PMID: 29341979
Wilson disease: lessons from an island population.
Tanner S. Tanner S. J Pediatr Gastroenterol Nutr. 2012 Jan;54(1):6-7. doi: 10.1097/MPG.0b013e3182301328. J Pediatr Gastroenterol Nutr. 2012. PMID: 21832954 No abstract available.
Glycogen storage disease type IX: High variability in clinical phenotype.
Beauchamp NJ, Dalton A, Ramaswami U, Niinikoski H, Mention K, Kenny P, Kolho KL, Raiman J, Walter J, Treacy E, Tanner S, Sharrard M. Beauchamp NJ, et al. Among authors: tanner s. Mol Genet Metab. 2007 Sep-Oct;92(1-2):88-99. doi: 10.1016/j.ymgme.2007.06.007. Epub 2007 Aug 3. Mol Genet Metab. 2007. PMID: 17689125
Diagnosis and phenotypic classification of Wilson disease.
Ferenci P, Caca K, Loudianos G, Mieli-Vergani G, Tanner S, Sternlieb I, Schilsky M, Cox D, Berr F. Ferenci P, et al. Among authors: tanner s. Liver Int. 2003 Jun;23(3):139-42. doi: 10.1034/j.1600-0676.2003.00824.x. Liver Int. 2003. PMID: 12955875 Review.
Portal vein cavernoma associated with goldenhar syndrome.
Stringer MD, Tovar JA, McKiernan PJ, Tanner S. Stringer MD, et al. Among authors: tanner s. J Pediatr Gastroenterol Nutr. 2005 Sep;41(3):368-70. doi: 10.1097/01.mpg.0000174333.85463.4f. J Pediatr Gastroenterol Nutr. 2005. PMID: 16132000 No abstract available.
579 results