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Mitochondrion
|
December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy
S Bannwarth, V Procaccio, C Rouzier, et al.
Neurology
|
October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2
J C de Greef, R J L F Lemmers, P Camaño, et al.
Neurology
|
December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
P Richard, K Gaudon, H Haddad, et al.
Neurology
|
August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1
I Pénisson-Besnier, M Devillers, R Porcher, et al.
Journal of Neurology
|
November 1, 2023
Quantitative brainstem and spinal MRI in amyotrophic lateral sclerosis: implications for predicting noninvasive ventilation needs
M Khamaysa, M Lefort, M Pélégrini-Issac, et al.
Revue Neurologique
|
August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]
V Humbertclaude, D Hamroun, M-C Picot, et al.
Revue Neurologique
|
February 17, 2009
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?]
V Meininger, J-C Antoine, M C Arne-Bes, et al.
European Journal of Neurology
|
August 2, 2025
Prevalence of SOD1 and C9orf72 Variants Among French ALS Population: The GENIALS Study
P Corcia, D Erazo, M D M Amador, et al.
Page
of 12
Search research articles
Search
Showing results (111-120 of 118) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 118 results.
Mitochondrion
|
December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy
S Bannwarth, V Procaccio, C Rouzier, et al.
Neurology
|
October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2
J C de Greef, R J L F Lemmers, P Camaño, et al.
Neurology
|
December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
P Richard, K Gaudon, H Haddad, et al.
Neurology
|
August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1
I Pénisson-Besnier, M Devillers, R Porcher, et al.
Journal of Neurology
|
November 1, 2023
Quantitative brainstem and spinal MRI in amyotrophic lateral sclerosis: implications for predicting noninvasive ventilation needs
M Khamaysa, M Lefort, M Pélégrini-Issac, et al.
Revue Neurologique
|
August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]
V Humbertclaude, D Hamroun, M-C Picot, et al.
Revue Neurologique
|
February 17, 2009
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?]
V Meininger, J-C Antoine, M C Arne-Bes, et al.
European Journal of Neurology
|
August 2, 2025
Prevalence of SOD1 and C9orf72 Variants Among French ALS Population: The GENIALS Study
P Corcia, D Erazo, M D M Amador, et al.
Page
of 12