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T Maisonobe

Showing results (101-110 of 122) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|September 7, 2001
Severe perturbations of the blood T cell repertoire in polymyositis, but not dermatomyositis patientsO Benveniste, P Chérin, T Maisonobe, et al.
Revue Neurologique|July 31, 1998
[Multifocal motor neuropathies with conduction blocks. 39 cases]N Le Forestier, B Chassande, A Moulonguet, et al.
Heart (British Cardiac Society)|July 16, 2004
Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic surveyP Charron, E Villard, P Sébillon, et al.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathyR Zemmouri, H Azzedine, S Assami, et al.
La Revue De Medecine Interne|November 26, 2016
[Neurosarcoidosis: Diagnosis and therapeutic issues]F Cohen Aubart, D Galanaud, J Haroche, et al.
Clinical and Experimental Immunology|March 8, 2002
Increased soluble p55 and p75 tumour necrosis factor-alpha receptors in patients with hepatitis C-associated mixed cryoglobulinaemiaG Kaplanski, V Marin, T Maisonobe, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 5, 2016
Pembrolizumab-induced necrotic myositis in a patient with metastatic melanomaH Vallet, A Gaillet, N Weiss, et al.
Journal of Medical Genetics|March 4, 2005
Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11A De Sandre-Giovannoli, V Delague, T Hamadouche, et al.
European Journal of Neurology|February 18, 2017
Phenotypic spectrum of Charcot-Marie-Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patientsR Guimarães-Costa, R Iancu Ferfoglia, S Leonard-Louis, et al.
Pageof 13

Showing results (101-110 of 122) with videos related to

Sort By:
Pageof 13
Journal of Immunology (Baltimore, Md. : 1950)|September 7, 2001
Severe perturbations of the blood T cell repertoire in polymyositis, but not dermatomyositis patientsO Benveniste, P Chérin, T Maisonobe, et al.
Revue Neurologique|July 31, 1998
[Multifocal motor neuropathies with conduction blocks. 39 cases]N Le Forestier, B Chassande, A Moulonguet, et al.
Heart (British Cardiac Society)|July 16, 2004
Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic surveyP Charron, E Villard, P Sébillon, et al.
Neurology|May 5, 1998
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic studyN Birouk, E LeGuern, T Maisonobe, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathyR Zemmouri, H Azzedine, S Assami, et al.
La Revue De Medecine Interne|November 26, 2016
[Neurosarcoidosis: Diagnosis and therapeutic issues]F Cohen Aubart, D Galanaud, J Haroche, et al.
Clinical and Experimental Immunology|March 8, 2002
Increased soluble p55 and p75 tumour necrosis factor-alpha receptors in patients with hepatitis C-associated mixed cryoglobulinaemiaG Kaplanski, V Marin, T Maisonobe, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 5, 2016
Pembrolizumab-induced necrotic myositis in a patient with metastatic melanomaH Vallet, A Gaillet, N Weiss, et al.
Journal of Medical Genetics|March 4, 2005
Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11A De Sandre-Giovannoli, V Delague, T Hamadouche, et al.
European Journal of Neurology|February 18, 2017
Phenotypic spectrum of Charcot-Marie-Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patientsR Guimarães-Costa, R Iancu Ferfoglia, S Leonard-Louis, et al.
Pageof 13