Kolexia
Stojkovic Tanja
Neurologie
Hôpital Pitie Salpetriere
Paris, France
205 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Maladies musculaires Dystrophies musculaires Dystrophies musculaires des ceintures Dystrophie myotonique Syndromes myasthéniques congénitaux Maladies neuromusculaires Maladie de Charcot-Marie-Tooth Maladies des dents Myopathies distales

Industries

B3TSI
77 collaboration(s)
Dernière en 2023
EXAFIELD
37 collaboration(s)
Dernière en 2023
Schlesinger Group France
27 collaboration(s)
Dernière en 2023
Biogen
12 collaboration(s)
Dernière en 2023

Dernières activités

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
P283 Natural history of limb girdle muscular dystrophy R9: one-year follow-up of a European cohort
Neuromuscular disorders : NMD   01 octobre 2023
P166 Deciphering the genetic cause of oculopharyngodistal myopathy in a French cohort using Cas9-targeted long-read sequencing
Neuromuscular disorders : NMD   01 octobre 2023
P351 Rhabdomyolysis and muscle biopsy outcomes: a single center retrospective cohort
Neuromuscular disorders : NMD   01 octobre 2023
P125 Quantitative MRI in upper limb muscles of patients with dysferlinopathy: 6-months and 12-months longitudinal data from the natural history Jain COS 2 project
Neuromuscular disorders : NMD   01 octobre 2023
P156 Muscle biopsy findings in a large cohort of patients affected by valosin containing protein disease: preliminary analysis of the international multicentric VCP study
Neuromuscular disorders : NMD   01 octobre 2023
P281 Quality of life in adults with dysferlinopathy: international clinical outcome study of dysferlinopathy
Neuromuscular disorders : NMD   01 octobre 2023
P69 Scoping review on the assessment tools used on SMA adolescent and adult patients
Neuromuscular disorders : NMD   01 octobre 2023
VP429 Impaired skeletal muscle strength in adult patients with laminopathies
Neuromuscular disorders : NMD   01 octobre 2023
P158 Heterozygous SPTAN1 frameshift mutations cause distal myopathy with neurogenic features
Neuromuscular disorders : NMD   01 octobre 2023