Les Centres Maladies Rares en Neurologie ont-ils changé les pratiques et la prise en charge de la maladie de Wilson ?
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference16 articles.
1. Molecular analysis of Wilson patients: Direct sequencing and MLPA analysis in the ATP7B gene and Atox1 and COMMD1 gene analysis;Bost;J Trace Elem Med Biol,2012
2. Late neurological presentations of Wilson disease patients in French population and identification of 8 novel mutations in the ATP7B gene;Chappuis;J Trace Elem Med Biol,2007
3. Determination of ultrafiltrable and exchangeable copper in plasma: stability and reference values in healthy subjects;El Balkhi;Anal Bioanal Chem,2009
4. Relative exchangeable copper: a new highly sensitive and highly specific biomarker for Wilson's disease diagnosis;El Balkhi;Clin Chim Acta,2011
5. Elucidation of the ATP7B N-domain Mg2+-ATP coordination site and its allosteric regulation;Hercend;PLoS One,2011
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Monitoring of Medical Therapy and Copper End Points;Wilson Disease;2019
2. L’observance dans la maladie de Wilson : intérêt d’un suivi rapproché au long cours;La Revue de Médecine Interne;2018-03
3. Unidades multidisciplinarias en hospitales de referencia para mejorar la atención de los pacientes con enfermedad de Wilson;Gastroenterología y Hepatología;2016-11
4. Multidisciplinary units in tertiary referral hospitals to improve management of Wilson disease;Gastroenterología y Hepatología (English Edition);2016-11
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