Kolexia
Walther-Louvier Ulrike
Pédiatrie
Hôpital Gui de Chauliac
Montpellier, France
63 Activités
5 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Dystrophies musculaires Maladies musculaires Myopathie de Duchenne Cardiomyopathies Défaillance cardiaque Amyotrophie spinale Atrophie Amyotrophie Amyotrophies spinales infantiles

Industries

Novartis
8 collaboration(s)
Dernière en 2023
Sanofi
4 collaboration(s)
Dernière en 2021
Roche
4 collaboration(s)
Dernière en 2023
Ipsos (France)
2 collaboration(s)
Dernière en 2023

Dernières activités

Effect of nusinersen after 3 years of treatment in 57 young children with SMA in terms of SMN2 copy number or type.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie   21 décembre 2023
OPALE: Observatoire Des Patients Atteints de Laminopathies et Emerinopathies (Observatory for PAtients With Laminopathies and Emerinopathies)
Essai Clinique (Hôpital Pitie Salpetriere)   13 décembre 2023
Confirmatory validation of the french version of the Duchenne Muscular Dystrophy module of the pediatric quality of life inventory (PedsQL 3.0DMDfv).
BMC pediatrics   15 novembre 2023
Long-term follow-up of 64 children with classical infantile-onset Pompe disease since 2004: A French real-life observational study.
European journal of neurology   10 juin 2023
HINT1-Neuropathy in France: Let’s expand genotypic and phenotypic spectrum
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference   01 mai 2023
A new score combining compound muscle action potential (CMAP) amplitudes and motor score is predictive of motor outcome after AVXS-101 (Onasemnogene Abeparvovec) SMA therapy.
Neuromuscular disorders : NMD   11 février 2023
HINT1 neuropathy: Expanding the genotype and phenotype spectrum.
Clinical genetics   16 août 2022
Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis: The French Experience.
Neurology   21 mars 2022
Association between prophylactic angiotensin-converting enzyme inhibitors and overall survival in Duchenne muscular dystrophy-analysis of registry data
FCPC 2020-2021   01 septembre 2021
An Integrated Clinical-Biological Approach to Identify Interindividual Variability and Atypical Phenotype-Genotype Correlations in Myopathies: Experience on A Cohort of 156 Families.
Genes   31 juillet 2021