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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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J F Hurtevent

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Neuromuscular Disorders : NMD|June 16, 2005

A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsiesH Zéphir, T Stojkovic, P Latour, et al.

Revue D'Electroencephalographie Et De Neurophysiologie Clinique|March 1, 1987

[Study of congenital hemiplegia: value of x-ray computed tomography of the brain and of somatosensory evoked potentials]F Gottrand, L Gottrand-Delannoy, L Vallée, et al.

Revue Neurologique|December 19, 2002

[Bilateral phrenic nerve paralysis, dysautonomia and restrictive cardiomyopathy in a case of POEMS syndrome]S Delalande, T Stojkovic, C Rose, et al.

Journal of Neurology|July 5, 2001

Guillain-Barré syndrome resembling brainstem death in a patient with brain injuryT Stojkovic, M Verdin, J F Hurtevent, et al.

Revue D'Electroencephalographie Et De Neurophysiologie Clinique|April 1, 1979

[Correlations between intracranial pressure variations and EEG changes in patients with cranial trauma (author's transl)]J D Guieu, M Lapierre, S Blond, et al.

Neuromuscular Disorders : NMD|April 21, 2006

A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classificationD Ferriby, T Stojkovic, D Sternberg, et al.

Neurophysiologie Clinique = Clinical Neurophysiology|December 8, 2009

A-delta and C-fibres function in primary restless legs syndromeL Tyvaert, E Laureau, J-P Hurtevent, et al.

Presse Medicale (Paris, France : 1983)|April 25, 1992

[Therapeutic efficacy of polyvalent immunoglobulins in autoimmune Lambert-Eaton's syndrome]C Rose, E Hachulla, J F Hurtevent, et al.

Revue Neurologique|November 1, 1995

[Acute and reversible myoclonic encephalopathy, extrapyramidal syndrome, polyneuropathy caused by chronic disulfiram poisoning]J De Sèze, D Caparros-Lefebvre, J B Nkenjuo, et al.

Annals of Physical and Rehabilitation Medicine|August 29, 2009

The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlersE Cetin, J M Cuisset, V Tiffreau, et al.

Pageof 5

Search research articles

Showing results (21-30 of 50) with videos related to

Sort By:

Pageof 5

Neuromuscular Disorders : NMD|June 16, 2005

A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsiesH Zéphir, T Stojkovic, P Latour, et al.

Revue D'Electroencephalographie Et De Neurophysiologie Clinique|March 1, 1987

[Study of congenital hemiplegia: value of x-ray computed tomography of the brain and of somatosensory evoked potentials]F Gottrand, L Gottrand-Delannoy, L Vallée, et al.

Revue Neurologique|December 19, 2002

[Bilateral phrenic nerve paralysis, dysautonomia and restrictive cardiomyopathy in a case of POEMS syndrome]S Delalande, T Stojkovic, C Rose, et al.

Journal of Neurology|July 5, 2001

Guillain-Barré syndrome resembling brainstem death in a patient with brain injuryT Stojkovic, M Verdin, J F Hurtevent, et al.

Revue D'Electroencephalographie Et De Neurophysiologie Clinique|April 1, 1979

[Correlations between intracranial pressure variations and EEG changes in patients with cranial trauma (author's transl)]J D Guieu, M Lapierre, S Blond, et al.

Neuromuscular Disorders : NMD|April 21, 2006

A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classificationD Ferriby, T Stojkovic, D Sternberg, et al.

Neurophysiologie Clinique = Clinical Neurophysiology|December 8, 2009

A-delta and C-fibres function in primary restless legs syndromeL Tyvaert, E Laureau, J-P Hurtevent, et al.

Presse Medicale (Paris, France : 1983)|April 25, 1992

[Therapeutic efficacy of polyvalent immunoglobulins in autoimmune Lambert-Eaton's syndrome]C Rose, E Hachulla, J F Hurtevent, et al.

Revue Neurologique|November 1, 1995

[Acute and reversible myoclonic encephalopathy, extrapyramidal syndrome, polyneuropathy caused by chronic disulfiram poisoning]J De Sèze, D Caparros-Lefebvre, J B Nkenjuo, et al.

Annals of Physical and Rehabilitation Medicine|August 29, 2009

The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlersE Cetin, J M Cuisset, V Tiffreau, et al.

Pageof 5