Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Nadège Girardot"'
Publikováno v:
Current treatment options in neurology. 20(11)
The aim of this article was to review the different sleep disorders associated with Wilson’s disease (WD), their mechanisms and their treatments. Some of these disorders such as REM sleep behavior disorder or sleepiness can appear as a prodromal ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dc57a5694c98aab3186cebaf89996c3
https://pubmed.ncbi.nlm.nih.gov/30259205
https://pubmed.ncbi.nlm.nih.gov/30259205
Publikováno v:
Revue neurologique. 174(9)
In brief, the classic form of Wilson's disease (WD) is an autosomal-recessive condition with hepatic, neurologic, psychiatric and systemic manifestations. However, the diagnosis should not be excluded because of a family history consistent with autos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0c13fc304569220c0555b419d1a012d
https://pubmed.ncbi.nlm.nih.gov/30249412
https://pubmed.ncbi.nlm.nih.gov/30249412
Publikováno v:
Revue Neurologique. 175:S123-S124
Introduction La maladie de Wilson se manifeste par divers symptomes hepatiques ou extrahepatiques avec un âge moyen de diagnostic de 18,5 ± 11 ans d’apres le registre Wilson France. Peu de donnees existent sur les formes a debut tardif. Objectifs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef47b22448e018377b640aa18040bdc0
https://doi.org/10.1016/j.neurol.2019.01.326
https://doi.org/10.1016/j.neurol.2019.01.326
Autor:
Jean-Marc Trocello, Karima Osmani, Michaela Pernon, Gérard Chevaillier, Claire de Brugière, Pascal Remy, Emilie Wenisch, Catherine Cousin, Nadège Girardot-Tinant, France Woimant
Publikováno v:
Dysphagia. 30:489-495
Hypersialorrhea, corresponding to excessive salivation is a symptom frequently reported in Wilson's disease, especially in its neurological form. The prevalence of this frequent complaint has not been often evaluated. During a 7-month period, 87 cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b66e3b26f62f4c01feaa60e5e05dbd7
https://doi.org/10.1007/s00455-015-9627-0
https://doi.org/10.1007/s00455-015-9627-0
Autor:
Aurélia Poujois, France Woimant, Solène Samson, Pascal Chaine, Nadège Girardot-Tinant, Philippe Tuppin
Publikováno v:
Clinics and research in hepatology and gastroenterology. 42(1)
Summary Background and aims Only a few epidemiological studies on the incidence and prevalence of Wilson's disease (WD) have been performed to date, and the results vary widely according to the reports. The aim of the study was to investigate the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec569967a49a399d6bf8887d1a1e488d
https://pubmed.ncbi.nlm.nih.gov/28648494
https://pubmed.ncbi.nlm.nih.gov/28648494
Autor:
Aurélia Poujois, Nouzha Djebrani-Oussedik, Nadège Girardot, Pascal Chaine, Joël Poupon, France Woimant
Publikováno v:
Revue Neurologique. 174:S121-S122
Introduction La maladie de Wilson (MW) entraine une surcharge en cuivre hepatique puis multisystemique si elle n’est pas traitee a vie. Une carence en cuivre (CaCu) par depletion therapeutique est possible. Objectifs Determiner la frequence des car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1074c1a08e08432a5122ac8fc63ef782
https://doi.org/10.1016/j.neurol.2018.01.275
https://doi.org/10.1016/j.neurol.2018.01.275
Publikováno v:
Revue Neurologique. 175:S111
Introduction La maladie de Wilson (MW) est une affection genetique rare due a une accumulation systemique de cuivre. Un registre national permet de collecter les donnees rares et precieuses des patients. Objectifs Decrire la cohorte de patients Wilso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2143a6cb35a8c5fd61f765006d10a1d1
https://doi.org/10.1016/j.neurol.2019.01.294
https://doi.org/10.1016/j.neurol.2019.01.294
Autor:
Jean-Marc Trocello, Souleiman El Balkhi, France Woimant, Nadège Girardot-Tinant, Philippe Chappuis, Carla Lloyd, Joël Poupon
Publikováno v:
Movement Disorders. 29:558-562
Background Family screening is a main step for the diagnosis in Wilson disease. This study was undertaken to evaluate the value of relative exchangeable copper for family screening. Methods Data from family screening were collected from the French Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::051472d763b7ddbfbf0ba6044cddf6b5
https://doi.org/10.1002/mds.25763
https://doi.org/10.1002/mds.25763
Autor:
Nadège Girardot-Tinant, Maud Bezier, Marc Polivka, Michel Ribojad, Pascal Chaine, Aurélia Poujois, France Woimant
Publikováno v:
Revue Neurologique. 173:S143-S144
Introduction Les manifestations cutanees associees a la maladie de Wilson (MW) et en particulier les anomalies des fibres elastiques (FE) ont fait l’objet de quelques cases reports. Objectifs Evaluer la frequence et decrire les elastopathies cutane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed97bd677b3c30d9b360aee92ccff81
https://doi.org/10.1016/j.neurol.2017.01.260
https://doi.org/10.1016/j.neurol.2017.01.260
Autor:
Frédéric Checler, Peter St George-Hyslop, Nadège Girardot, Raphaëlle Pardossi-Piquard, Jean Sevalle, Bruno Vincent, Toshitaka Kawarai, Claire Sunyach, Cristine Alves da Costa
Publikováno v:
Current Alzheimer Research. 4:423-426
Amyloid beta-peptide (Abeta), which plays a central role in Alzheimer Disease, is generated by presenilin-dependent and presenilin-independent gamma-secretase cleavages of beta-amyloid precursor protein (betaAPP). We report that the presenilins (PS1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd96e80d3d62d017d1aa05938d0b1461
https://doi.org/10.2174/156720507781788945
https://doi.org/10.2174/156720507781788945