Kolexia
Lazaro Leila Pédiatrie
Lazaro Leila
Pédiatrie
Centre Hospitalier de la Côte Basque
Bayonne, France
38 Activités
0 Followers
Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Accident vasculaire cérébral Maladies musculaires Encéphalopathies Épilepsie Infarctus Encéphalopathie ischémique Paralysie Accident vasculaire cérébral ischémique Infarctus cérébral

Collaborateurs

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Odent Sylvie
Odent Sylvie
Hôpital Sud Rennes, Rennes, France
Ferreiro-Sieiro Ana
Ferreiro-Sieiro Ana
Hôpital Pitie Salpetriere, Paris, France
Rivera Serge
Rivera Serge
Centre Hospitalier de la Côte Basque, Bayonne, France
Goizet Cyril
Goizet Cyril
Hôpital Pellegrin, Bordeaux, France

Industries

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Sanofi
2 collaboration(s)
Dernière en 2023
THE SURGICAL COMPANY SAS
1 collaboration(s)
Dernière en 2022
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Dernières activités

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"Helping Those in Need" Mrs. International Abu Dhabi 2023 ... - Facebook
Facebook   31 janvier 2023
Poster No: 64b
Abstracts of the 2022 Peripheral Nerve Society Annual Meeting   11 juillet 2022
From Negative to Positive Diagnosis: Structural Variation Could Be the Second Mutation You Are Looking for in a Recessive Autosomal Gene.
Journal of personalized medicine   03 février 2022
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families.
Genetics in medicine : official journal of the American College of Medical Genetics   07 juillet 2021
Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency.
Journal of medical genetics   18 mars 2021
Early-onset epileptic encephalopathy related to germline PIGA mutations: A series of 5 cases.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society   28 juin 2020
Congenital Titinopathy: Comprehensive characterization and pathogenic insights.
Annals of neurology   12 août 2019
Delineating syndrome: From congenital microcephaly to hyperkinetic encephalopathy.
Neurology. Genetics   07 novembre 2018
Loss-of-function mutation of TRIP4 causes a novel form of congenital muscle disease and reveals the transcription coactivator ASC-1 as a new regulator of skeletal myogenesis
21st International Congress of the World Muscle Society   01 octobre 2016
Multimodal Outcome at 7 Years of Age after Neonatal Arterial Ischemic Stroke.
The Journal of pediatrics   09 mars 2016