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BMC Medicine
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March 22, 2013
Quantifiable diagnosis of muscular dystrophies and neurogenic atrophies through network analysis
Aurora Sáez, Eloy Rivas, Adoración Montero-Sánchez, et al.
Muscle & Nerve
|
May 10, 2005
X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterization
Carmen Paradas, Celedonio Márquez, Eduard Gallardo, et al.
Brain Communications
|
March 27, 2026
Excitotoxicity in amyotrophic lateral sclerosis: a key pathogenic mechanism
Silvia Silva-Hucha, Rosendo G Hernández, Diego Baena-López, et al.
Stem Cell Research
|
October 17, 2017
Generation of an induced pluripotent stem cell line (CSCRMi001-A) from a patient with a new type of limb-girdle muscular dystrophy (LGMD) due to a missense mutation in POGLUT1 (Rumi)
Jianbo Wu, Samuel D Hunt, Nadine Matthias, et al.
JAMA Neurology
|
November 20, 2013
Branching enzyme deficiency: expanding the clinical spectrum
Carmen Paradas, Hasan O Akman, Carolina Ionete, et al.
Revista Espanola De Enfermedades Digestivas
|
January 6, 2012
Thalidomide with peginterferon alfa-2b and ribavirin in the treatment of non-responders genotype 1 chronic hepatitis C patients: proof of concept
Benjamin Pardo-Yules, Rocío Gallego-Durán, Mohammed Eslam, et al.
Annals of Clinical and Translational Neurology
|
October 16, 2019
NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay
Fabiola Mavillard, Marcos Madruga-Garrido, Eloy Rivas, 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.
Brain Communications
|
June 19, 2026
Efficacy and safety of pyrimidine nucleos(t)ide therapy in thymidine kinase 2 deficiency
Michio Hirano, Caterina Garone, Richard Haas, et al.
BMC Neurology
|
February 2, 2023
Lessons learned from a sporadic FUSopathy in a young man: a case report
Ernesto García-Roldán, Eloy Rivas-Infante, Manuel Medina-Rodríguez, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 83) with videos related to
Sort By:
Page
of 9
BMC Medicine
|
March 22, 2013
Quantifiable diagnosis of muscular dystrophies and neurogenic atrophies through network analysis
Aurora Sáez, Eloy Rivas, Adoración Montero-Sánchez, et al.
Muscle & Nerve
|
May 10, 2005
X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterization
Carmen Paradas, Celedonio Márquez, Eduard Gallardo, et al.
Brain Communications
|
March 27, 2026
Excitotoxicity in amyotrophic lateral sclerosis: a key pathogenic mechanism
Silvia Silva-Hucha, Rosendo G Hernández, Diego Baena-López, et al.
Stem Cell Research
|
October 17, 2017
Generation of an induced pluripotent stem cell line (CSCRMi001-A) from a patient with a new type of limb-girdle muscular dystrophy (LGMD) due to a missense mutation in POGLUT1 (Rumi)
Jianbo Wu, Samuel D Hunt, Nadine Matthias, et al.
JAMA Neurology
|
November 20, 2013
Branching enzyme deficiency: expanding the clinical spectrum
Carmen Paradas, Hasan O Akman, Carolina Ionete, et al.
Revista Espanola De Enfermedades Digestivas
|
January 6, 2012
Thalidomide with peginterferon alfa-2b and ribavirin in the treatment of non-responders genotype 1 chronic hepatitis C patients: proof of concept
Benjamin Pardo-Yules, Rocío Gallego-Durán, Mohammed Eslam, et al.
Annals of Clinical and Translational Neurology
|
October 16, 2019
NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay
Fabiola Mavillard, Marcos Madruga-Garrido, Eloy Rivas, 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.
Brain Communications
|
June 19, 2026
Efficacy and safety of pyrimidine nucleos(t)ide therapy in thymidine kinase 2 deficiency
Michio Hirano, Caterina Garone, Richard Haas, et al.
BMC Neurology
|
February 2, 2023
Lessons learned from a sporadic FUSopathy in a young man: a case report
Ernesto García-Roldán, Eloy Rivas-Infante, Manuel Medina-Rodríguez, et al.
Page
of 9