Kolexia
Petit Francois Pharmacien
Petit Francois
Pharmacien
Centre Antoine Lacassagne
Nice, France
76 Activités
0 Followers
Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Glycogénose Maladies musculaires Glycogénose de type III Glycogénose de type V Faiblesse musculaire Délétion de segment de chromosome Maladies métaboliques Glycogénose de type VII Myalgie

Collaborateurs

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Laforet Pascal
Laforet Pascal
Hôpital Raymond-Poincaré, Garches, France
Labrune Philippe
Labrune Philippe
Hôpital Antoine-Béclère, Clamart, France
Eymard Bruno
Eymard Bruno
Hôpital Pitie Salpetriere, Paris, France
Tachdjian Gerard
Tachdjian Gerard
Hôpital Antoine-Béclère, Clamart, France

Industries

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AstraZeneca
1 collaboration(s)
Dernière en 2021
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Dernières activités

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Objective evaluation of clinical actionability for genes involved in myopathies: 63 genes with a medical value for patient care
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
French recommendations for the management of glycogen storage disease type III.
European journal of medical research   24 juillet 2023
Targeting Harvey rat sarcoma viral oncogene homolog in head and neck cancer: how to move forward?
Current opinion in oncology   17 mars 2023
Glycogénose de type I
HAS Publications   13 décembre 2022
Management of copy number variants associated with incomplete penetrance and variable expressivity-Results of a French survey.
Clinical genetics   09 novembre 2022
Objective Evaluation of Clinical Actionability for Genes Involved in Myopathies: 63 Genes with a Medical Value for Patient Care.
International journal of molecular sciences   31 juillet 2022
VINILO: PHASE I-II STUDY OF VINBLASTINE IN COMBINATION WITH NILOTINIB IN CHILDREN, ADOLESCENTS, AND YOUNG ADULTS WITH REFRACTORY OR RECURRENT LOW-GRADE GLIOMA
Essai Clinique (Gustave-Roussy)   24 mai 2022
First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15.
Taiwanese journal of obstetrics & gynecology   04 avril 2022
Objective evaluation of clinical actionnability for genes involved in myopathies: 51 promising genes
Abstracts from the 54th European Society of Human Genetics (ESHG) Conference   01 avril 2022
Whole-body muscle MRI in McArdle disease.
Neuromuscular disorders : NMD   05 août 2021