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S Teijeira

Showing results (11-20 of 19) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycanopathy (LGMD 2E) in a Spanish familyE Rivas, S Teijeira, M R dos Santos, et al.
QJM : Monthly Journal of the Association of Physicians|October 12, 2010
Shrinking lung syndrome caused by lupus myopathyL A Pérez-de-Llano, O Castro-Añón, M J López, et al.
Clinical Neuropathology|April 10, 2009
Myoadenylate deaminase deficiency: clinico-pathological and molecular study of a series of 27 Spanish casesS Teijeira, B San Millán, J M Fernández, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patientsF Calvo, S Teijeira, J M Fernandez, et al.
Revista De Neurologia|July 11, 1998
[Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification]S Teijeira-Bautista, D García-García, A Teijeiro-Ferreira, et al.
Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Brain : a Journal of Neurology|April 29, 2005
Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large familyM J Sobrido, J M Fernández, E Fontoira, et al.
Annals of Neurology|November 15, 2001
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation studyM A Martín, J C Rubio, J Buchbinder, et al.
Revista De Neurologia|July 11, 1998
[Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases]D García-García, S Teijeira-Bautista, J M Fernández-Rodríguez, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycanopathy (LGMD 2E) in a Spanish familyE Rivas, S Teijeira, M R dos Santos, et al.
QJM : Monthly Journal of the Association of Physicians|October 12, 2010
Shrinking lung syndrome caused by lupus myopathyL A Pérez-de-Llano, O Castro-Añón, M J López, et al.
Clinical Neuropathology|April 10, 2009
Myoadenylate deaminase deficiency: clinico-pathological and molecular study of a series of 27 Spanish casesS Teijeira, B San Millán, J M Fernández, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patientsF Calvo, S Teijeira, J M Fernandez, et al.
Revista De Neurologia|July 11, 1998
[Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification]S Teijeira-Bautista, D García-García, A Teijeiro-Ferreira, et al.
Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Brain : a Journal of Neurology|April 29, 2005
Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large familyM J Sobrido, J M Fernández, E Fontoira, et al.
Annals of Neurology|November 15, 2001
Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation studyM A Martín, J C Rubio, J Buchbinder, et al.
Revista De Neurologia|July 11, 1998
[Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases]D García-García, S Teijeira-Bautista, J M Fernández-Rodríguez, et al.
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