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Human Molecular Genetics
|
January 1, 1996
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
E LeGuern, R Gouider, N Ravisé, et al.
Neurology
|
December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities
R Gouider, E LeGuern, J Emile, et al.
American Journal of Human Genetics
|
June 1, 1996
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group
J Lopes, E LeGuern, R Gouider, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
October 31, 2023
Optineurin in patients with Amyotrophic Lateral Sclerosis associated to atypical Parkinsonism in Tunisian population
I Kacem, I Sghaier, S Peverelli, 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.
Human Molecular Genetics
|
September 1, 1995
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group
E LeGuern, R Gouider, J Lopes, 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.
Revue Neurologique
|
March 8, 2024
Retinal changes in multiple sclerosis: An optical coherence tomography and angiography study
S Mrabet, Y Falfoul, M Bouassida, et al.
Revue Neurologique
|
May 26, 1999
[Neurological manifestations indicative of brucellosis]
R Gouider, S Samet, C Triki, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 51) with videos related to
Sort By:
Page
of 6
Human Molecular Genetics
|
January 1, 1996
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
E LeGuern, R Gouider, N Ravisé, et al.
Neurology
|
December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities
R Gouider, E LeGuern, J Emile, et al.
American Journal of Human Genetics
|
June 1, 1996
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group
J Lopes, E LeGuern, R Gouider, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
October 31, 2023
Optineurin in patients with Amyotrophic Lateral Sclerosis associated to atypical Parkinsonism in Tunisian population
I Kacem, I Sghaier, S Peverelli, 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.
Human Molecular Genetics
|
September 1, 1995
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group
E LeGuern, R Gouider, J Lopes, 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.
Revue Neurologique
|
March 8, 2024
Retinal changes in multiple sclerosis: An optical coherence tomography and angiography study
S Mrabet, Y Falfoul, M Bouassida, et al.
Revue Neurologique
|
May 26, 1999
[Neurological manifestations indicative of brucellosis]
R Gouider, S Samet, C Triki, et al.
Page
of 6