Search research articles
Contact Us
Filters
Showing results (101-110 of 136) with videos related to
Page
of 14
Sort By:
Plos One
|
November 19, 2008
Gene expression profiling in limb-girdle muscular dystrophy 2A
Amets Sáenz, Margarita Azpitarte, Rubén Armañanzas, et al.
Annals of Clinical and Translational Neurology
|
July 30, 2019
Identification of serum microRNAs as potential biomarkers in Pompe disease
Ana Carrasco-Rozas, Esther Fernández-Simón, Maria Cinta Lleixà, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 18, 2021
Isolation of human fibroadipogenic progenitors and satellite cells from frozen muscle biopsies
Xavier Suárez-Calvet, Esther Fernández-Simón, Patricia Piñol-Jurado, et al.
Cell Death & Disease
|
July 12, 2018
Nintedanib decreases muscle fibrosis and improves muscle function in a murine model of dystrophinopathy
Patricia Piñol-Jurado, Xavier Suárez-Calvet, Esther Fernández-Simón, et al.
Annals of Neurology
|
January 8, 2014
Atypical phenotypes in titinopathies explained by second titin mutations
Anni Evilä, Anna Vihola, Jaakko Sarparanta, et al.
The American Journal of Pathology
|
May 23, 2022
BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients
Ana Carrasco-Rozas, Esther Fernández-Simón, Xavier Suárez-Calvet, et al.
The Lancet. Neurology
|
November 19, 2020
COVID-19-associated risks and effects in myasthenia gravis (CARE-MG)
Srikanth Muppidi, Jeffrey T Guptill, Saiju Jacob, et al.
Annals of Neurology
|
March 10, 2011
Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia
Eric Lancaster, Maartje G M Huijbers, Vered Bar, et al.
Annals of Clinical and Translational Neurology
|
June 22, 2018
The impact of rituximab infusion protocol on the long-term outcome in anti-MuSK myasthenia gravis
Elena Cortés-Vicente, Ricard Rojas-Garcia, Jordi Díaz-Manera, et al.
Annals of Clinical and Translational Neurology
|
July 22, 2025
Repeat Expansions in PLIN4 Cause Autosomal Dominant Vacuolar Myopathy With Sarcolemmal Features
Laura Llansó, Igor Stevanovski, Germán Morís, et al.
Page
of 14
Search research articles
Search
Showing results (101-110 of 136) with videos related to
Sort By:
Page
of 14
Plos One
|
November 19, 2008
Gene expression profiling in limb-girdle muscular dystrophy 2A
Amets Sáenz, Margarita Azpitarte, Rubén Armañanzas, et al.
Annals of Clinical and Translational Neurology
|
July 30, 2019
Identification of serum microRNAs as potential biomarkers in Pompe disease
Ana Carrasco-Rozas, Esther Fernández-Simón, Maria Cinta Lleixà, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 18, 2021
Isolation of human fibroadipogenic progenitors and satellite cells from frozen muscle biopsies
Xavier Suárez-Calvet, Esther Fernández-Simón, Patricia Piñol-Jurado, et al.
Cell Death & Disease
|
July 12, 2018
Nintedanib decreases muscle fibrosis and improves muscle function in a murine model of dystrophinopathy
Patricia Piñol-Jurado, Xavier Suárez-Calvet, Esther Fernández-Simón, et al.
Annals of Neurology
|
January 8, 2014
Atypical phenotypes in titinopathies explained by second titin mutations
Anni Evilä, Anna Vihola, Jaakko Sarparanta, et al.
The American Journal of Pathology
|
May 23, 2022
BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients
Ana Carrasco-Rozas, Esther Fernández-Simón, Xavier Suárez-Calvet, et al.
The Lancet. Neurology
|
November 19, 2020
COVID-19-associated risks and effects in myasthenia gravis (CARE-MG)
Srikanth Muppidi, Jeffrey T Guptill, Saiju Jacob, et al.
Annals of Neurology
|
March 10, 2011
Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia
Eric Lancaster, Maartje G M Huijbers, Vered Bar, et al.
Annals of Clinical and Translational Neurology
|
June 22, 2018
The impact of rituximab infusion protocol on the long-term outcome in anti-MuSK myasthenia gravis
Elena Cortés-Vicente, Ricard Rojas-Garcia, Jordi Díaz-Manera, et al.
Annals of Clinical and Translational Neurology
|
July 22, 2025
Repeat Expansions in PLIN4 Cause Autosomal Dominant Vacuolar Myopathy With Sarcolemmal Features
Laura Llansó, Igor Stevanovski, Germán Morís, et al.
Page
of 14