Deciphering the natural history of SCA7 in children

Autor: Bruno Leheup, Anneke J.A. Kievit, Y. Capri, Cécile Cazeneuve, P. Comet‐Didierjean, Claire Ewenczyk, David Devos, Delphine Héron, Diana Rodriguez, M. Barathon, M. Carneiro, C. Barondiot, I. Strubi‐Villaume, G. Lesca, Isabelle Audo, R. van Minkelen, Agnese Suppiej, F. Dubois, A. Curie, N. Allani‐Essid, M. G. Bah, L. Ratbi, Cyril Mignot, F. Klapczynski, Joel Victor Fluss, Alexandra Durr, C. Gitiaux, Fanny Mochel, Isabelle Meunier, J. Do Cao, Perrine Charles, S. Pichard, D. Gras, Agathe Roubertie

Publikováno v: EUROPEAN JOURNAL OF NEUROLOGY
EUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 (11), pp.2267-2276. ⟨10.1111/ene.14405⟩
European Journal of Neurology, 27(11), 2267-2276. Wiley-Blackwell Publishing Ltd
European Journal of Neurology, Vol. 27, No 11 (2020) pp. 2267-2276

International audience; BACKGROUND AND PURPOSE: Childhood-onset autosomal dominant cerebellar ataxia type 7 (SCA7) is a severe disease which leads to premature loss of ambulation and death. Early diagnosis of SCA7 is of major importance for genetic c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7c82cd877098db1f920ca565b3591e3
https://hal.science/hal-03939353

Maturation par bêtaméthasone au cours d'une grossesse de femme présentant un diabète compliqué: le mieux est-il l'ennemi du bien?

Autor: G.-A. Sery, R. Vieux, M. Floriot, Olivier Morel, C. Barondiot, Jean-Michel Hascoet

Publikováno v: Archives de Pédiatrie. 14:989-992

Diabetic pregnancy is a precarious situation, both for mother and fetus, because it increases the risk of prematurity and respiratory distress. We report 3 cases of severe acute complications following antenatal betamethasone treatment in mothers pre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c6c1188f7a0b29a40eb6186a515af9f5
https://doi.org/10.1016/j.arcped.2007.03.025

Age-related features of HHV-6 central nervous system infection

Autor: H. Jeulin, B. Girard, C. Bilbault, H. Mecili, C. Barondiot, E. Raffo, E. Schmitt

Publikováno v: European Journal of Paediatric Neurology. 21:e122

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::28ad3066c1b825150f840161e69fe7e0
https://doi.org/10.1016/j.ejpn.2017.04.980

[Specific remedial therapy in a specialist unit: evaluation of 31 children with severe, specific language or reading disorders over one academic year]

Autor: D, Coste-Zeitoun, F, Pinton, C, Barondiot, B, Ducot, J, Warszawski, C, Billard

Publikováno v: Revue neurologique. 161(3)

Up to 3 percent of the children in France present severe and specific language and/or reading disorders, despite regular remedial therapies. Few studies have measured the effectiveness of treatment administered in a specialist unit.The aims of this s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2e28484dd7341e532292ffc2c1265f3b
https://pubmed.ncbi.nlm.nih.gov/15800451

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