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Revue Neurologique
|
January 23, 1999
[Cervical deficit radiculopathy in 3 cases of vertebral artery dissection]
J M de Bray, I Penisson-Besnier, M Giroud, et al.
La Revue De Medecine Interne
|
November 26, 2008
[Cutaneous EBV-associated lymphoproliferative disorder in a dermatomyositis treated with immunosuppressive agents]
M Steff, Y Le Corre, I Penisson-Besnier, et al.
Annals of Physical and Rehabilitation Medicine
|
August 28, 2009
Contraception and screening for cervical and breast cancer in neuromuscular disease: a retrospective study of 50 patients monitored at a clinical reference centre
S Goutard, C Baron, C Bouton, et al.
Cerebrovascular Diseases (Basel, Switzerland)
|
February 25, 2000
Cervical artery dissections in the puerperium: pathogenic hypotheses concerning seven observations
J M de Bray, B Guillon, J P Neau, et al.
Clinical Genetics
|
November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay
M Krahn, C Pécheux, F Chapon, et al.
Revue Neurologique
|
September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease
P Laforêt, K Laloui, B Granger, et al.
Revue Neurologique
|
January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]
R Ben Yaou, H-M Bécane, L Demay, et al.
Neurology
|
May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy
B Eymard, N B Romero, F Leturcq, et al.
Annals of Neurology
|
August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
G Bonne, E Mercuri, A Muchir, et al.
Revue Neurologique
|
July 14, 2010
[Management of muscle and nerve biopsies: expert guidelines from two French professional societies, Société française de myologie et de l'Association française contre les myopathies]
E Uro-Soste, C Fernandez, F-J Authier, et al.
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Search research articles
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Showing results (21-30 of 30) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 30 results.
Revue Neurologique
|
January 23, 1999
[Cervical deficit radiculopathy in 3 cases of vertebral artery dissection]
J M de Bray, I Penisson-Besnier, M Giroud, et al.
La Revue De Medecine Interne
|
November 26, 2008
[Cutaneous EBV-associated lymphoproliferative disorder in a dermatomyositis treated with immunosuppressive agents]
M Steff, Y Le Corre, I Penisson-Besnier, et al.
Annals of Physical and Rehabilitation Medicine
|
August 28, 2009
Contraception and screening for cervical and breast cancer in neuromuscular disease: a retrospective study of 50 patients monitored at a clinical reference centre
S Goutard, C Baron, C Bouton, et al.
Cerebrovascular Diseases (Basel, Switzerland)
|
February 25, 2000
Cervical artery dissections in the puerperium: pathogenic hypotheses concerning seven observations
J M de Bray, B Guillon, J P Neau, et al.
Clinical Genetics
|
November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay
M Krahn, C Pécheux, F Chapon, et al.
Revue Neurologique
|
September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease
P Laforêt, K Laloui, B Granger, et al.
Revue Neurologique
|
January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]
R Ben Yaou, H-M Bécane, L Demay, et al.
Neurology
|
May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy
B Eymard, N B Romero, F Leturcq, et al.
Annals of Neurology
|
August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
G Bonne, E Mercuri, A Muchir, et al.
Revue Neurologique
|
July 14, 2010
[Management of muscle and nerve biopsies: expert guidelines from two French professional societies, Société française de myologie et de l'Association française contre les myopathies]
E Uro-Soste, C Fernandez, F-J Authier, et al.
Page
of 3