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European Journal of Public Health
|
June 18, 2026
Physical activity for small- and medium-sized enterprises: what features work in real life? A Delphi study
Sebastià Mas-Alòs, Frank Vandaele, Estela Farías, et al.
Journal of Medical Genetics
|
December 19, 2022
Genetic diagnosis of Duchenne and Becker muscular dystrophy through mRNA analysis: new splicing events
Alba Segarra-Casas, Cristina Domínguez-González, Aurelio Hernández-Laín, et al.
Frontiers in Immunology
|
February 6, 2023
Acute and long-term immune responses to SARS-CoV-2 infection in unvaccinated children and young adults with inborn errors of immunity
Ana García-García, Claudia Fortuny, Victoria Fumadó, et al.
Neuromuscular Disorders : NMD
|
August 22, 2020
Early and long-term effect of the treatment with pyridostigmine in patients with GMPPB-related congenital myasthenic syndrome
Edna Julieth Bobadilla-Quesada, Daniel Natera-de Benito, Laura Carrera-García, et al.
Annals of Clinical and Translational Neurology
|
September 26, 2025
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Gregorio A Nolasco, Mònica Roldán, Yalda Jamshidi, et al.
Clinical Chemistry
|
August 5, 2021
Circulating Cell-Free Mitochondrial DNA in Cerebrospinal Fluid as a Biomarker for Mitochondrial Diseases
Selena Trifunov, Abraham J Paredes-Fuentes, Carmen Badosa, et al.
Neuropathology and Applied Neurobiology
|
June 9, 2025
MYL1-Related Congenital Myopathy: Clinical, Genetic and Pathological Insights
Irene Madrigal, Cristina Villar-Vera, Gemma Arca, et al.
Epilepsia
|
April 9, 2020
Epilepsy in LAMA2-related muscular dystrophy: An electro-clinico-radiological characterization
Daniel Natera-de Benito, Jordi Muchart, Debora Itzep, et al.
Cell Death & Disease
|
September 6, 2023
Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations
Xavier Suárez-Calvet, Esther Fernández-Simón, Daniel Natera, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2019
CHRNG-related nonlethal multiple pterygium syndrome: Muscle imaging pattern and clinical, histopathological, and molecular genetic findings
Laura Carrera-García, Daniel Natera-de Benito, Klaus Dieterich, et al.
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Search research articles
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Showing results (31-40 of 49) with videos related to
Sort By:
Page
of 5
European Journal of Public Health
|
June 18, 2026
Physical activity for small- and medium-sized enterprises: what features work in real life? A Delphi study
Sebastià Mas-Alòs, Frank Vandaele, Estela Farías, et al.
Journal of Medical Genetics
|
December 19, 2022
Genetic diagnosis of Duchenne and Becker muscular dystrophy through mRNA analysis: new splicing events
Alba Segarra-Casas, Cristina Domínguez-González, Aurelio Hernández-Laín, et al.
Frontiers in Immunology
|
February 6, 2023
Acute and long-term immune responses to SARS-CoV-2 infection in unvaccinated children and young adults with inborn errors of immunity
Ana García-García, Claudia Fortuny, Victoria Fumadó, et al.
Neuromuscular Disorders : NMD
|
August 22, 2020
Early and long-term effect of the treatment with pyridostigmine in patients with GMPPB-related congenital myasthenic syndrome
Edna Julieth Bobadilla-Quesada, Daniel Natera-de Benito, Laura Carrera-García, et al.
Annals of Clinical and Translational Neurology
|
September 26, 2025
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Gregorio A Nolasco, Mònica Roldán, Yalda Jamshidi, et al.
Clinical Chemistry
|
August 5, 2021
Circulating Cell-Free Mitochondrial DNA in Cerebrospinal Fluid as a Biomarker for Mitochondrial Diseases
Selena Trifunov, Abraham J Paredes-Fuentes, Carmen Badosa, et al.
Neuropathology and Applied Neurobiology
|
June 9, 2025
MYL1-Related Congenital Myopathy: Clinical, Genetic and Pathological Insights
Irene Madrigal, Cristina Villar-Vera, Gemma Arca, et al.
Epilepsia
|
April 9, 2020
Epilepsy in LAMA2-related muscular dystrophy: An electro-clinico-radiological characterization
Daniel Natera-de Benito, Jordi Muchart, Debora Itzep, et al.
Cell Death & Disease
|
September 6, 2023
Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations
Xavier Suárez-Calvet, Esther Fernández-Simón, Daniel Natera, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2019
CHRNG-related nonlethal multiple pterygium syndrome: Muscle imaging pattern and clinical, histopathological, and molecular genetic findings
Laura Carrera-García, Daniel Natera-de Benito, Klaus Dieterich, et al.
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of 5