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C Verny

Showing results (41-50 of 57) with videos related to

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Cancer Chemotherapy and Pharmacology|January 29, 2019
Cyclophosphamide dose adjustment based on body weight and albuminemia in elderly patients treated with R-mini-CHOPE Baudry, S Huguet, A L Couderc, et al.
Neurology|July 7, 2010
High insulinlike growth factor I is associated with cognitive decline in Huntington diseaseN Saleh, S Moutereau, J-P Azulay, et al.
Journal Des Maladies Vasculaires|January 1, 1989
[Popliteal venous aneurysm revealed by recurring pulmonary embolism. Echographic, phlebographic, x-ray computed tomographic and nuclear magnetic resonance aspects]C De Gennes, C Verny, I Ankri, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Annales D'Urologie|January 1, 1990
[Prostatic location as the manifestation of lymphoma]C de Gennes, J M Ziza, C Verny, et al.
Neuropathology and Applied Neurobiology|July 21, 2020
STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brainP Codron, F Letournel, S Marty, et al.
Neuroimage|August 1, 2006
Distribution of grey matter atrophy in Huntington's disease patients: a combined ROI-based and voxel-based morphometric studyG Douaud, V Gaura, M-J Ribeiro, et al.
Human Molecular Genetics|February 7, 2001
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth diseaseA Guilbot, A Williams, N Ravisé, et al.
Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Neuromolecular Medicine|June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth diseaseO Dubourg, H Azzedine, C Verny, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Cancer Chemotherapy and Pharmacology|January 29, 2019
Cyclophosphamide dose adjustment based on body weight and albuminemia in elderly patients treated with R-mini-CHOPE Baudry, S Huguet, A L Couderc, et al.
Neurology|July 7, 2010
High insulinlike growth factor I is associated with cognitive decline in Huntington diseaseN Saleh, S Moutereau, J-P Azulay, et al.
Journal Des Maladies Vasculaires|January 1, 1989
[Popliteal venous aneurysm revealed by recurring pulmonary embolism. Echographic, phlebographic, x-ray computed tomographic and nuclear magnetic resonance aspects]C De Gennes, C Verny, I Ankri, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Annales D'Urologie|January 1, 1990
[Prostatic location as the manifestation of lymphoma]C de Gennes, J M Ziza, C Verny, et al.
Neuropathology and Applied Neurobiology|July 21, 2020
STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brainP Codron, F Letournel, S Marty, et al.
Neuroimage|August 1, 2006
Distribution of grey matter atrophy in Huntington's disease patients: a combined ROI-based and voxel-based morphometric studyG Douaud, V Gaura, M-J Ribeiro, et al.
Human Molecular Genetics|February 7, 2001
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth diseaseA Guilbot, A Williams, N Ravisé, et al.
Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Neuromolecular Medicine|June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth diseaseO Dubourg, H Azzedine, C Verny, et al.
Pageof 6