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The Journal of Pathology
|
August 1, 2012
The increase of pericyte population in human neuromuscular disorders supports their role in muscle regeneration in vivo
Jordi Díaz-Manera, Eduard Gallardo, Noemi de Luna, et al.
Journal of Neurology
|
March 18, 2008
Antibodies against disialosyl and terminal NeuNAc(alpha2-3)Gal ganglioside epitopes in acute relapsing sensory ataxic neuropathy
Ricard Rojas-Garcia, Eduard Gallardo, Monica Povedano, et al.
Journal of Neuropathology and Experimental Neurology
|
September 6, 2018
Effect of MAPK Inhibition on the Differentiation of a Rhabdomyosarcoma Cell Line Combined With CRISPR/Cas9 Technology: An In Vitro Model of Human Muscle Diseases
Noemí De Luna, Xavier Suarez-Calvet, Maialen Garicano, et al.
Clinical Endocrinology
|
September 27, 2003
Neuromuscular dysfunction in adult growth hormone deficiency
Susan M Webb, Irene de Andrés-Aguayo, Ricard Rojas-García, et al.
Stem Cells and Development
|
June 20, 2013
Bone marrow transplantation in dysferlin-deficient mice results in a mild functional improvement
Bàrbara Flix, Xavier Suárez-Calvet, Jordi Díaz-Manera, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 23, 2012
1α,25(OH)(2)-Vitamin D3 increases dysferlin expression in vitro and in a human clinical trial
Noemi De Luna, Jordi Díaz-Manera, Carmen Paradas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 4, 2009
Bulbar involvement in patients with antiganglioside antibodies against NeuNAc(alpha2-3)Gal
Ricard Rojas-Garcia, Eduard Gallardo, Noemi De Luna, et al.
Journal of Neuroimmunology
|
May 19, 2006
A novel antiganglioside specificity against terminal NeuNAc(alfa 2-3)Gal in acute bulbar palsy
Ricard Rojas-Garcia, Maria Martinez-Lage, Eduard Gallardo, et al.
The American Journal of Pathology
|
June 16, 2017
Platelet-Derived Growth Factor BB Influences Muscle Regeneration in Duchenne Muscle Dystrophy
Patricia Piñol-Jurado, Eduard Gallardo, Noemi de Luna, et al.
Neuromuscular Disorders : NMD
|
July 16, 2018
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement
Lidia Gonzalez-Quereda, Eduard Gallardo, Ana Töpf, et al.
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of 14
Search research articles
Search
Showing results (51-60 of 136) with videos related to
Sort By:
Page
of 14
The Journal of Pathology
|
August 1, 2012
The increase of pericyte population in human neuromuscular disorders supports their role in muscle regeneration in vivo
Jordi Díaz-Manera, Eduard Gallardo, Noemi de Luna, et al.
Journal of Neurology
|
March 18, 2008
Antibodies against disialosyl and terminal NeuNAc(alpha2-3)Gal ganglioside epitopes in acute relapsing sensory ataxic neuropathy
Ricard Rojas-Garcia, Eduard Gallardo, Monica Povedano, et al.
Journal of Neuropathology and Experimental Neurology
|
September 6, 2018
Effect of MAPK Inhibition on the Differentiation of a Rhabdomyosarcoma Cell Line Combined With CRISPR/Cas9 Technology: An In Vitro Model of Human Muscle Diseases
Noemí De Luna, Xavier Suarez-Calvet, Maialen Garicano, et al.
Clinical Endocrinology
|
September 27, 2003
Neuromuscular dysfunction in adult growth hormone deficiency
Susan M Webb, Irene de Andrés-Aguayo, Ricard Rojas-García, et al.
Stem Cells and Development
|
June 20, 2013
Bone marrow transplantation in dysferlin-deficient mice results in a mild functional improvement
Bàrbara Flix, Xavier Suárez-Calvet, Jordi Díaz-Manera, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 23, 2012
1α,25(OH)(2)-Vitamin D3 increases dysferlin expression in vitro and in a human clinical trial
Noemi De Luna, Jordi Díaz-Manera, Carmen Paradas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 4, 2009
Bulbar involvement in patients with antiganglioside antibodies against NeuNAc(alpha2-3)Gal
Ricard Rojas-Garcia, Eduard Gallardo, Noemi De Luna, et al.
Journal of Neuroimmunology
|
May 19, 2006
A novel antiganglioside specificity against terminal NeuNAc(alfa 2-3)Gal in acute bulbar palsy
Ricard Rojas-Garcia, Maria Martinez-Lage, Eduard Gallardo, et al.
The American Journal of Pathology
|
June 16, 2017
Platelet-Derived Growth Factor BB Influences Muscle Regeneration in Duchenne Muscle Dystrophy
Patricia Piñol-Jurado, Eduard Gallardo, Noemi de Luna, et al.
Neuromuscular Disorders : NMD
|
July 16, 2018
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement
Lidia Gonzalez-Quereda, Eduard Gallardo, Ana Töpf, et al.
Page
of 14