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Revue Neurologique|December 1, 1995

[Progressive lupus dementia. 2 cases with or without antiphospholipid antibodies]C Robin, P M Gonnaud, I Durieu, et al.

La Revue De Medecine Interne|January 1, 1997

[Paraneoplastic intestinal pseudo-occlusion and sensory neuronopathy disclosing small-cell bronchial cancer]C Khouatra, J Honnorat, P Bombaron, et al.

Acta Neurologica Scandinavica|October 1, 1995

DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutationsP M Gonnaud, F Sturtz, Y Fourbil, et al.

Muscle & Nerve|July 7, 2000

Exercise test in muscle channelopathies and other muscle disordersT Kuntzer, F Flocard, C Vial, et al.

Cytogenetics and Cell Genetics|January 1, 1994

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)E Le Guern, F Sturtz, M Gugenheim, et al.

European Neurology|January 1, 1996

Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France NetworkF G Sturtz, F Chauvin, E Ollagnon-Roman, et al.

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Showing results (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

Revue Neurologique|December 1, 1995

[Progressive lupus dementia. 2 cases with or without antiphospholipid antibodies]C Robin, P M Gonnaud, I Durieu, et al.

La Revue De Medecine Interne|January 1, 1997

[Paraneoplastic intestinal pseudo-occlusion and sensory neuronopathy disclosing small-cell bronchial cancer]C Khouatra, J Honnorat, P Bombaron, et al.

Acta Neurologica Scandinavica|October 1, 1995

DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutationsP M Gonnaud, F Sturtz, Y Fourbil, et al.

Muscle & Nerve|July 7, 2000

Exercise test in muscle channelopathies and other muscle disordersT Kuntzer, F Flocard, C Vial, et al.

Cytogenetics and Cell Genetics|January 1, 1994

Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)E Le Guern, F Sturtz, M Gugenheim, et al.

European Neurology|January 1, 1996

Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France NetworkF G Sturtz, F Chauvin, E Ollagnon-Roman, et al.

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