Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Eduardo Couchonnal"'
Autor:
Peter Ott, Thomas Sandahl, Aftab Ala, David Cassiman, Eduardo Couchonnal-Bedoya, Rubens Gisbert Cury, Anna Czlonkowska, Gerald Denk, Renata D’Inca, Francisco de Assis Aquino Gondim, Joanna Moore, Aurelia Poujois, Carlos Alexandre Twardowschy, Karl Heinz Weiss, Massimo Zuin, C.Omar F. Kamlin, Michael L. Schilsky
Publikováno v:
JHEP Reports, Vol 6, Iss 8, Pp 101115- (2024)
Background & Aims: Wilson disease (WD) is caused by accumulation of copper primarily in the liver and brain. During maintenance therapy of WD with D-penicillamine, current guidelines recommend on-treatment ranges of urinary copper excretion (UCE) of
Externí odkaz:
https://doaj.org/article/90b27145c7244d369bafae9917758cfd
Autor:
Olivier Guillaud, Alain Lachaux, Justin Mbala, Abdelouahed Belmalih, Eduardo Couchonnal Bedoya
Publikováno v:
BMJ Open Gastroenterology, Vol 10, Iss 1 (2023)
Introduction Wilson’s disease (WD) is a copper metabolism disorder characterised by a progressive accumulation of this metal mainly in the liver and the brain. Treatment is based on the removal of copper operated by the chelators, among which, D-pe
Externí odkaz:
https://doaj.org/article/a4f75c2e3d9448a49fc9da5ad472a786
Publikováno v:
Diagnostics, Vol 13, Iss 2, p 256 (2023)
Wilson disease and alpha1-antitrypsin deficiency are two rare genetic diseases that may impact predominantly the liver and/or the brain, and the liver and/or the lung, respectively. The early diagnosis of these diseases is important in order to initi
Externí odkaz:
https://doaj.org/article/988a984f95d84b2b843928e603e148a6
Autor:
Abbassi, Nadia, Bourrahouat, Aicha, Bedoya, Eduardo Couchonnal, Pagan, Cécile, Qabli, Meriem El, Maidoumi, Sana, Belmalih, Abdelouahed, Guillaud, Olivier, Kissani, Najib, Abkari, Abdelhak, Chahid, Imane, Rafai, Mohammed Abdoh, Mouane, Nezha, Kriouile, Yamna, Aidi, Saadia, Hida, Moustpha, Idrissi, Mounia Lakhdar, Belahsen, Mohammed Faouzi, Abkari, Mohammed El, Rkain, Maria, Ismaili, Zahi, Sedki, Azeddine, Bost, Muriel, Aboussair, Nisrine, Lachaux, Alain
Publikováno v:
In Clinics and Research in Hepatology and Gastroenterology May 2024 48(5)
Autor:
Michael L Schilsky, Anna Czlonkowska, Massimo Zuin, David Cassiman, Carlos Twardowschy, Aurelia Poujois, Francisco de Assis A Gondim, Gerald Denk, Rubens G Cury, Peter Ott, Joanna Moore, Aftab Ala, Renata D'Inca, Eduardo Couchonnal-Bedoya, Koenraad D'Hollander, Nicolas Dubois, C Omar F Kamlin, Karl Heinz Weiss, Uyen To, Amar Patel, Daksshi Hettiarachchi, Alessia Giorgini, Sara Monico, Tomasz Litwin, Agnieszka Piechal, Marta Skowronska, Alain Lachaux, Abdelouahed Belmalih, Alexandra Boogers, Isabelle Mohr, Andrea Langel, Christian Freitas, Egberto Reis Barbosa, Thomas D Sandahl, Lisbet Gerdes, Alexandre Obadia, Djamila Rahli, Jeremy Cosgrove
Publikováno v:
CHELATE trial investigators 2022, ' Trientine tetrahydrochloride versus penicillamine for maintenance therapy in Wilson disease (CHELATE) : a randomised, open-label, non-inferiority, phase 3 trial ', The Lancet Gastroenterology and Hepatology, vol. 7, no. 12, pp. 1092-1102 . https://doi.org/10.1016/S2468-1253(22)00270-9
Background: Wilson disease is an inherited disorder of copper transport. Whereas penicillamine is used therapeutically to re-establish copper balance, trientine is indicated for patients with penicillamine intolerance. We aimed to compare penicillami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc08a6d996987fd1d2dba0c63b14f359
https://pure.au.dk/portal/da/publications/trientine-tetrahydrochloride-versus-penicillamine-for-maintenance-therapy-in-wilson-disease-chelate(ba317b8b-40a9-4b06-9881-6e93f059c2ea).html
https://pure.au.dk/portal/da/publications/trientine-tetrahydrochloride-versus-penicillamine-for-maintenance-therapy-in-wilson-disease-chelate(ba317b8b-40a9-4b06-9881-6e93f059c2ea).html
Autor:
Dany Hermann Ngwanou, Eduardo Couchonnal, François Parant, Abdelouahed Belmalih, Olivier Guillaud, Jérôme Dumortier, Muriel Bost, Alain Lachaux
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 75(4)
Determining 24-hour urinary copper excretion (UCE) levels is useful for diagnosing Wilson's disease (WD) and for treatment monitoring. Exchangeable copper (ExC) is a novel potential marker, but its long-term changes have never been described in patie
Autor:
Eduardo Couchonnal, Sophie Bouchard, Thomas Damgaard Sandahl, Cecile Pagan, Laurence Lion-François, Olivier Guillaud, Dalila Habes, Dominique Debray, Thierry Lamireau, Pierre Broué, Alexandre Fabre, Claire Vanlemmens, Rodolphe Sobesky, Frederic Gottrand, Laure Bridoux-Henno, Abdelouahed Belmalih, Aurelia Poujois, Corinne Collet, Micheline Misrahi, Bruno Francou, Anne Sophie Brunet, Alain Lachaux, Muriel Bost
Publikováno v:
Couchonnal, E, Bouchard, S, Sandahl, T D, 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, A S, Lachaux, A & Bost, M 2021, ' Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64(10) (2021) 104305] ', European Journal of Medical Genetics, vol. 64, no. 11, pp. 104341 . https://doi.org/10.1016/j.ejmg.2021.104341
European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2021, 64 (11), pp.104341. ⟨10.1016/j.ejmg.2021.104341⟩
European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2021, 64 (11), pp.104341. ⟨10.1016/j.ejmg.2021.104341⟩
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34a648abc67dca1b7458242e2fc0865d
http://hdl.handle.net/20.500.12278/123774
http://hdl.handle.net/20.500.12278/123774
Autor:
Mbala, Justin, Belmalih, Abdelouahed, Guillaud, Olivier, Lachaux, Alain, Bedoya, Eduardo Couchonnal
Publikováno v:
BMJ Open Gastroenterology; 2023, Vol. 10 Issue 1, p1-4, 4p
Autor:
Guillaume Petit, Paul Jaulent, Eduardo Couchonnal-Bedoya, Olivier Guillaud, Stéphane Thobois, Chloé Laurencin
Publikováno v:
Revue neurologique. 178(4)
Autor:
Pierre Broué, Anne Sophie Brunet, Dominique Debray, Alain Lachaux, Muriel Bost, Abdelouahed Belmalih, Thierry Lamireau, Eduardo Couchonnal, Olivier Guillaud, Claire Vanlemmens, Dalila Habes, Frédéric Gottrand, Laurence Lion-François, Aurélia Poujois, Jérôme Dumortier, Emmanuel Jacquemin, Alexandre Fabre, Rodolphe Sobesky, Laure Bridoux-Henno
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, ⟨10.1097/mpg.0000000000003196⟩
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, ⟨10.1097/mpg.0000000000003196⟩
OBJECTIVES To describe a cohort of Wilson disease (WD) pediatric cases, and to point out the diagnostic particularities of this age group and the long-term outcome. METHODS Clinical data of 182 pediatric patients included in the French WD national re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aab9f3bd34236e7e2308481f18d82264
http://hdl.handle.net/20.500.12278/109258
http://hdl.handle.net/20.500.12278/109258