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Page 1
Exchangeable copper: a reflection of the neurological severity in Wilson's disease.
Poujois A, Trocello JM, Djebrani-Oussedik N, Poupon J, Collet C, Girardot-Tinant N, Sobesky R, Habès D, Debray D, Vanlemmens C, Fluchère F, Ory-Magne F, Labreuche J, Preda C, Woimant F. Poujois A, et al. Among authors: sobesky r. Eur J Neurol. 2017 Jan;24(1):154-160. doi: 10.1111/ene.13171. Epub 2016 Oct 14. Eur J Neurol. 2017. PMID: 27739240
Long term results of liver transplantation for Wilson's disease: experience in France.
Guillaud O, Dumortier J, Sobesky R, Debray D, Wolf P, Vanlemmens C, Durand F, Calmus Y, Duvoux C, Dharancy S, Kamar N, Boudjema K, Bernard PH, Pageaux GP, Salamé E, Gugenheim J, Lachaux A, Habes D, Radenne S, Hardwigsen J, Chazouillères O, Trocello JM, Woimant F, Ichai P, Branchereau S, Soubrane O, Castaing D, Jacquemin E, Samuel D, Duclos-Vallée JC. Guillaud O, et al. Among authors: sobesky r. J Hepatol. 2014 Mar;60(3):579-89. doi: 10.1016/j.jhep.2013.10.025. Epub 2013 Nov 6. J Hepatol. 2014. PMID: 24211743
Rapid and reliable diagnosis of Wilson disease using X-ray fluorescence.
Kaščáková S, Kewish CM, Rouzière S, Schmitt F, Sobesky R, Poupon J, Sandt C, Francou B, Somogyi A, Samuel D, Jacquemin E, Dubart-Kupperschmitt A, Nguyen TH, Bazin D, Duclos-Vallée JC, Guettier C, Le Naour F. Kaščáková S, et al. Among authors: sobesky r. J Pathol Clin Res. 2016 Jun 6;2(3):175-86. doi: 10.1002/cjp2.48. eCollection 2016 Jul. J Pathol Clin Res. 2016. PMID: 27499926 Free PMC article.
Liver transplantation as a rescue therapy for severe neurologic forms of Wilson disease.
Poujois A, Sobesky R, Meissner WG, Brunet AS, Broussolle E, Laurencin C, Lion-François L, Guillaud O, Lachaux A, Maillot F, Belin J, Salamé E, Vanlemmens C, Heyd B, Bellesme C, Habes D, Bureau C, Ory-Magne F, Chaine P, Trocello JM, Cherqui D, Samuel D, de Ledinghen V, Duclos-Vallée JC, Woimant F. Poujois A, et al. Among authors: sobesky r. Neurology. 2020 May 26;94(21):e2189-e2202. doi: 10.1212/WNL.0000000000009474. Epub 2020 May 12. Neurology. 2020. PMID: 32398357
Pediatric Wilson's Disease: Phenotypic, Genetic Characterization and Outcome of 182 Children in France.
Couchonnal E, Lion-François L, Guillaud O, Habes D, Debray D, Lamireau T, Broué P, Fabre A, Vanlemmens C, Sobesky R, Gottrand F, Bridoux-Henno L, Dumortier J, Belmalih A, Poujois A, Jacquemin E, Brunet AS, Bost M, Lachaux A. Couchonnal E, et al. Among authors: sobesky r. J Pediatr Gastroenterol Nutr. 2021 Oct 1;73(4):e80-e86. doi: 10.1097/MPG.0000000000003196. J Pediatr Gastroenterol Nutr. 2021. PMID: 34091542
Non-invasive diagnosis and follow-up of rare genetic liver diseases.
Sobesky R, Guillaud O, Bouzbib C, Sogni P, Poujois A, Woimant F, Duclos-Vallée JC, Bourlière M, de Lédinghen V, Ganne-Carrié N, Bureau C. Sobesky R, et al. Clin Res Hepatol Gastroenterol. 2022 Jan;46(1):101768. doi: 10.1016/j.clinre.2021.101768. Epub 2021 Jul 29. Clin Res Hepatol Gastroenterol. 2022. PMID: 34332127
Peripheral Arrangement of Steatosis Microvacuoles in Wilson's Disease.
Laurent-Bellue A, Sobesky R, Guettier C. Laurent-Bellue A, et al. Among authors: sobesky r. Clin Gastroenterol Hepatol. 2022 Apr;20(4):A17. doi: 10.1016/j.cgh.2021.08.005. Epub 2021 Aug 5. Clin Gastroenterol Hepatol. 2022. PMID: 34365001 No abstract available.
ATP7B variant spectrum in a French pediatric Wilson disease cohort.
Couchonnal E, Bouchard S, Sandahl TD, Pagan C, Lion-François L, Guillaud O, Habes D, Debray D, Lamireau T, Broué P, Fabre A, Vanlemmens C, Sobesky R, Gottrand F, Bridoux-Henno L, Belmalih A, Poujois A, Brunet AS, Lachaux A, Bost M. Couchonnal E, et al. Among authors: sobesky r. Eur J Med Genet. 2021 Oct;64(10):104305. doi: 10.1016/j.ejmg.2021.104305. Epub 2021 Aug 13. Eur J Med Genet. 2021. PMID: 34400371
Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64(10) (2021) 104305].
Couchonnal E, Bouchard S, Sandahl TD, Pagan C, Lion-François L, Guillaud O, Habes D, Debray D, Lamireau T, Broué P, Fabre A, Vanlemmens C, Sobesky R, Gottrand F, Bridoux-Henno L, Belmalih A, Poujois A, Brunet AS, Lachaux A, Bost M. Couchonnal E, et al. Among authors: sobesky r. Eur J Med Genet. 2021 Nov;64(11):104341. doi: 10.1016/j.ejmg.2021.104341. Epub 2021 Sep 20. Eur J Med Genet. 2021. PMID: 34544667 Free article. No abstract available.
Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64 (10) (October 2021) 104305].
Couchonnal E, Bouchard S, Sandahl TD, Pagan C, Lion-François L, Guillaud O, Habes D, Debray D, Lamireau T, Broué P, Fabre A, Vanlemmens C, Sobesky R, Gottrand F, Bridoux-Henno L, Belmalih A, Poujois A, Collet C, Francou B, Brunet AS, Lachaux A, Misrahi M, Bost M. Couchonnal E, et al. Among authors: sobesky r. Eur J Med Genet. 2022 Mar;65(3):104453. doi: 10.1016/j.ejmg.2022.104453. Epub 2022 Feb 16. Eur J Med Genet. 2022. PMID: 35183456 No abstract available.
48 results