Jean Pouget - Concepedia

Author

Jean Pouget

Also Known As

E. Salort-Campana, Emilien Delmont, Hacer Durmus, J POUGET, J Pouget, J. Pouget, Jean Pouget, Jean-Pascal Lefaucheur, POUGET J., Pouget, Jean

350

Publications

11.1K

Citations

H-Index

190

Concepts

All Affiliations

Hôpital de la Timone Inserm Sorbonne Université Centre National de la Recherche Scientifique Pitié-Salpêtrière Hospital

About

Jean Pouget is an author at Hôpital de la Timone specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	76	4.9K
2	Health Sciences	16	23	1.3K
3	Engineering	2	2	230
4	Natural Sciences	2	2	563
5	Public Health	2	2	89

Jean Pouget

143

Publications

10.1K

Citations

H-Index

Page 1

	Year	Citations
Nonmotor fluctuations in Parkinson’s disease Tatiana Witjas, Elsa Kaphan, J.-P. Azulay, Neurology	2002	624
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2 Maria-Ceù Moreira, Sandra Klur, Andrea H. Németh, Nature Genetics Yeast Rna HelicaseNatural SciencesGeneticsRna BiologyMolecular Biology	2004	518
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Brain Motor Neuron DiseaseGeneticsMitochondrial MyopathyAlzheimer's DiseaseMitochondrial Origin	2014	490
Visual control of locomotion in Parkinson's disease J.-P. Azulay, Serge Mesure, B. Amblard, Brain	1999	331
Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose study Ole B. Suhr, Teresa Coelho, Juan Buades, Orphanet Journal of Rare Diseases	2015	316
Phenotypic Study in 40 Patients With Dysferlin Gene Mutations Karine Nguyen, Guillaume Bassez, Martin Krahn, Archives of Neurology	2007	262
Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (PATH): a randomised, double-blind, placebo-controlled, phase 3 trial Ivo N. van Schaik, Vera Bril, Nan van Geloven, The Lancet Neurology Subcutaneous ImmunoglobulinAutoimmune DiseaseChronic InflammatoryMaintenance TreatmentImmunotherapy	2017	258
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients Mathieu Anheim, B. Monga, Marie‐Céline Fleury, Brain	2009	242
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, Brain Mitochondrial MyopathyGenome InstabilityMfn2 GeneMitochondrial FunctionOphthalmology	2011	234
Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy Johann Böhm, Frédéric Chevessier, A. Maues de Paula, The American Journal of Human Genetics MechanobiologyEngineeringConstitutive ActivationPhysiologyCytoskeleton	2013	208

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