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Acta Neuropathologica
|
May 8, 2003
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency
A Prelle, M Sciacco, L Tancredi, et al.
Journal of Neurology
|
November 10, 1998
A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia
L Franceschina, S Salani, A Bordoni, et al.
Neurology
|
December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardium
R Cagliani, N Bresolin, A Prelle, et al.
Journal of Inherited Metabolic Disease
|
April 10, 2009
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene
C Lamperti, S Salani, S Lucchiari, et al.
Annals of Neurology
|
February 5, 1998
Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease
G P Comi, A Bordoni, S Salani, et al.
Neurology
|
October 22, 1998
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
A Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.
Experimental Cell Research
|
June 14, 2002
A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouse
S Corti, S Strazzer, R Del Bo, et al.
European Journal of Neurology
|
February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
R Del Bo, S Ghezzi, S Corti, et al.
Neuromuscular Disorders : NMD
|
March 3, 2015
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family
I Colombo, S Pagliarani, S Testolin, et al.
European Journal of Neurology
|
October 14, 2017
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy
A Cortese, M Laurà, C Casali, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 84) with videos related to
Sort By:
Page
of 9
Acta Neuropathologica
|
May 8, 2003
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency
A Prelle, M Sciacco, L Tancredi, et al.
Journal of Neurology
|
November 10, 1998
A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia
L Franceschina, S Salani, A Bordoni, et al.
Neurology
|
December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardium
R Cagliani, N Bresolin, A Prelle, et al.
Journal of Inherited Metabolic Disease
|
April 10, 2009
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene
C Lamperti, S Salani, S Lucchiari, et al.
Annals of Neurology
|
February 5, 1998
Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease
G P Comi, A Bordoni, S Salani, et al.
Neurology
|
October 22, 1998
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
A Papadimitriou, G P Comi, G M Hadjigeorgiou, et al.
Experimental Cell Research
|
June 14, 2002
A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouse
S Corti, S Strazzer, R Del Bo, et al.
European Journal of Neurology
|
February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
R Del Bo, S Ghezzi, S Corti, et al.
Neuromuscular Disorders : NMD
|
March 3, 2015
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family
I Colombo, S Pagliarani, S Testolin, et al.
European Journal of Neurology
|
October 14, 2017
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy
A Cortese, M Laurà, C Casali, et al.
Page
of 9