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Neuromuscular Disorders : NMD
|
February 3, 1998
A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci
N B Romero, D Récan, O Rigal, et al.
BMC Veterinary Research
|
November 11, 2020
Tuberculosis caused by Mycobacterium caprae in a camel (Camelus dromedarius)
J A Infantes-Lorenzo, B Romero, A Rodríguez-Bertos, et al.
Actas Dermo-Sifiliograficas
|
May 15, 2022
Practical Update of the Guidelines Published by the Psoriasis Group of the Spanish Academy of Dermatology and Venereology (GPs) on the Treatment of Psoriasis With Biologic Agents: Part 2 - Management of Special Populations, Patients With Comorbid Conditions, and Risk
J M Carrascosa, L Puig, I B Romero, et al.
Transplantation Proceedings
|
August 10, 2010
Should a complex uropathy be a contraindication for renal transplantation in children?
A L González-Jorge, J A Hernández-Plata, E Bracho-Blanchet, et al.
Veterinary Journal (London, England : 1997)
|
March 4, 2019
A new test to detect antibodies against Mycobacterium tuberculosis complex in red deer serum
J Thomas, J A Infantes-Lorenzo, I Moreno, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Morphological studies of skeletal muscle in lactic acidosis
N B Romero, A Lombès, G Touati, et al.
Journal of Clinical Microbiology
|
November 26, 2020
Direct PCR on Tissue Samples To Detect Mycobacterium tuberculosis Complex: an Alternative to the Bacteriological Culture
V Lorente-Leal, E Liandris, M Pacciarini, et al.
The Journal of Clinical Investigation
|
August 1, 1993
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin
K Matsumura, F M Tomé, V Ionasescu, et al.
Neuromuscular Disorders : NMD
|
September 1, 2004
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actin
Carina Wallgren-Pettersson, Katarina Pelin, Kristen J Nowak, et al.
Neuromuscular Disorders : NMD
|
September 3, 2019
X-linked Emery-Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures
Marion Brisset, Rabah Ben Yaou, Robert-Yves Carlier, et al.
Page
of 34
Search research articles
Search
Showing results (171-180 of 337) with videos related to
Sort By:
Page
of 34
Neuromuscular Disorders : NMD
|
February 3, 1998
A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci
N B Romero, D Récan, O Rigal, et al.
BMC Veterinary Research
|
November 11, 2020
Tuberculosis caused by Mycobacterium caprae in a camel (Camelus dromedarius)
J A Infantes-Lorenzo, B Romero, A Rodríguez-Bertos, et al.
Actas Dermo-Sifiliograficas
|
May 15, 2022
Practical Update of the Guidelines Published by the Psoriasis Group of the Spanish Academy of Dermatology and Venereology (GPs) on the Treatment of Psoriasis With Biologic Agents: Part 2 - Management of Special Populations, Patients With Comorbid Conditions, and Risk
J M Carrascosa, L Puig, I B Romero, et al.
Transplantation Proceedings
|
August 10, 2010
Should a complex uropathy be a contraindication for renal transplantation in children?
A L González-Jorge, J A Hernández-Plata, E Bracho-Blanchet, et al.
Veterinary Journal (London, England : 1997)
|
March 4, 2019
A new test to detect antibodies against Mycobacterium tuberculosis complex in red deer serum
J Thomas, J A Infantes-Lorenzo, I Moreno, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Morphological studies of skeletal muscle in lactic acidosis
N B Romero, A Lombès, G Touati, et al.
Journal of Clinical Microbiology
|
November 26, 2020
Direct PCR on Tissue Samples To Detect Mycobacterium tuberculosis Complex: an Alternative to the Bacteriological Culture
V Lorente-Leal, E Liandris, M Pacciarini, et al.
The Journal of Clinical Investigation
|
August 1, 1993
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin
K Matsumura, F M Tomé, V Ionasescu, et al.
Neuromuscular Disorders : NMD
|
September 1, 2004
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actin
Carina Wallgren-Pettersson, Katarina Pelin, Kristen J Nowak, et al.
Neuromuscular Disorders : NMD
|
September 3, 2019
X-linked Emery-Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures
Marion Brisset, Rabah Ben Yaou, Robert-Yves Carlier, et al.
Page
of 34