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European Journal of Human Genetics : EJHG
|
December 22, 1999
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1
A Guilbot, N Ravisé, A Bouhouche, et al.
La Revue De Medecine Interne
|
July 28, 1999
[Macrophagic myofasciitis: description and etiopathogenic hypotheses. Study and Research Group on Acquired and Dysimmunity-related Muscular Diseases (GERMMAD) of the French Association against Myopathies (AFM)]
P Chérin, P Laforet, R K Ghérardi, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
September 22, 2014
Segmental somatosensory-evoked potentials as a diagnostic tool in chronic inflammatory demyelinating polyneuropathies, and other sensory neuropathies
R M Koutlidis, X Ayrignac, P-F Pradat, et al.
Brain : a Journal of Neurology
|
May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases
N Birouk, R Gouider, E Le Guern, et al.
Neurology
|
November 1, 1995
Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion
R Gouider, E LeGuern, M Gugenheim, et al.
Neurology
|
February 10, 2010
Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation
K G Claeys, T Maisonobe, J Böhm, et al.
Muscle & Nerve
|
January 12, 1999
Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease
P Sindou, J M Vallat, F Chapon, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2008
Two further cases of spondyloenchondrodysplasia (SPENCD) with immune dysregulation
V Navarro, C Scott, T A Briggs, et al.
Presse Medicale (Paris, France : 1983)
|
March 8, 2000
[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)]
P Chérin, P Laforêt, R K Ghérardi, et al.
Neurology
|
October 27, 2004
Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease
P Laforêt, P Charron, T Maisonobe, et al.
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Search research articles
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Showing results (91-100 of 122) with videos related to
Sort By:
Page
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European Journal of Human Genetics : EJHG
|
December 22, 1999
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1
A Guilbot, N Ravisé, A Bouhouche, et al.
La Revue De Medecine Interne
|
July 28, 1999
[Macrophagic myofasciitis: description and etiopathogenic hypotheses. Study and Research Group on Acquired and Dysimmunity-related Muscular Diseases (GERMMAD) of the French Association against Myopathies (AFM)]
P Chérin, P Laforet, R K Ghérardi, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
September 22, 2014
Segmental somatosensory-evoked potentials as a diagnostic tool in chronic inflammatory demyelinating polyneuropathies, and other sensory neuropathies
R M Koutlidis, X Ayrignac, P-F Pradat, et al.
Brain : a Journal of Neurology
|
May 1, 1997
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases
N Birouk, R Gouider, E Le Guern, et al.
Neurology
|
November 1, 1995
Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion
R Gouider, E LeGuern, M Gugenheim, et al.
Neurology
|
February 10, 2010
Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation
K G Claeys, T Maisonobe, J Böhm, et al.
Muscle & Nerve
|
January 12, 1999
Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease
P Sindou, J M Vallat, F Chapon, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2008
Two further cases of spondyloenchondrodysplasia (SPENCD) with immune dysregulation
V Navarro, C Scott, T A Briggs, et al.
Presse Medicale (Paris, France : 1983)
|
March 8, 2000
[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)]
P Chérin, P Laforêt, R K Ghérardi, et al.
Neurology
|
October 27, 2004
Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease
P Laforêt, P Charron, T Maisonobe, et al.
Page
of 13