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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 22, 2016
Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies
Paola Imbrici, Concetta Altamura, Giulia Maria Camerino, et al.
Annals of Clinical and Translational Neurology
|
December 15, 2021
Genetic defects are common in myopathies with tubular aggregates
Qiang Gang, Conceição Bettencourt, Stefen Brady, et al.
Nutrients
|
July 15, 2026
Gut Microbiota Composition and Plasma Metabolomic Profile Are Associated with Amyloid Pathology and Cognitive Performance in Patients with Mild Cognitive Impairment
Marina Mora-Ortiz, Magdalena P Cardelo, Esther Porras-Pérez, et al.
JAMA Neurology
|
April 7, 2015
Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy
Michela Ripolone, Dario Ronchi, Raffaella Violano, et al.
Journal of Molecular Neuroscience : MN
|
April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients
Daniela Piga, Francesca Magri, Dario Ronchi, et al.
EMBO Reports
|
March 7, 2018
Zc3h10 is a novel mitochondrial regulator
Matteo Audano, Silvia Pedretti, Gaia Cermenati, et al.
Nutrition & Diabetes
|
February 22, 2025
MiRNAs as biomarkers of nutritional therapy to achieve T2DM remission in patients with coronary heart disease: from the CORDIOPREV study
Juan Francisco Alcala-Diaz, Antonio Camargo, Cristina Vals-Delgado, et al.
Cardiovascular Diabetology
|
August 3, 2023
Plasma lipidic fingerprint associated with type 2 diabetes in patients with coronary heart disease: CORDIOPREV study
Alejandro Villasanta-Gonzalez, Marina Mora-Ortiz, Juan F Alcala-Diaz, et al.
Human Mutation
|
January 7, 2017
ORAI1 Mutations with Distinct Channel Gating Defects in Tubular Aggregate Myopathy
Johann Böhm, Monica Bulla, Jill E Urquhart, et al.
Science Translational Medicine
|
June 30, 2012
Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy
Francesco Saverio Tedesco, Mattia F M Gerli, Laura Perani, et al.
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of 13
Search research articles
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Showing results (91-100 of 122) with videos related to
Sort By:
Page
of 13
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 22, 2016
Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies
Paola Imbrici, Concetta Altamura, Giulia Maria Camerino, et al.
Annals of Clinical and Translational Neurology
|
December 15, 2021
Genetic defects are common in myopathies with tubular aggregates
Qiang Gang, Conceição Bettencourt, Stefen Brady, et al.
Nutrients
|
July 15, 2026
Gut Microbiota Composition and Plasma Metabolomic Profile Are Associated with Amyloid Pathology and Cognitive Performance in Patients with Mild Cognitive Impairment
Marina Mora-Ortiz, Magdalena P Cardelo, Esther Porras-Pérez, et al.
JAMA Neurology
|
April 7, 2015
Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy
Michela Ripolone, Dario Ronchi, Raffaella Violano, et al.
Journal of Molecular Neuroscience : MN
|
April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients
Daniela Piga, Francesca Magri, Dario Ronchi, et al.
EMBO Reports
|
March 7, 2018
Zc3h10 is a novel mitochondrial regulator
Matteo Audano, Silvia Pedretti, Gaia Cermenati, et al.
Nutrition & Diabetes
|
February 22, 2025
MiRNAs as biomarkers of nutritional therapy to achieve T2DM remission in patients with coronary heart disease: from the CORDIOPREV study
Juan Francisco Alcala-Diaz, Antonio Camargo, Cristina Vals-Delgado, et al.
Cardiovascular Diabetology
|
August 3, 2023
Plasma lipidic fingerprint associated with type 2 diabetes in patients with coronary heart disease: CORDIOPREV study
Alejandro Villasanta-Gonzalez, Marina Mora-Ortiz, Juan F Alcala-Diaz, et al.
Human Mutation
|
January 7, 2017
ORAI1 Mutations with Distinct Channel Gating Defects in Tubular Aggregate Myopathy
Johann Böhm, Monica Bulla, Jill E Urquhart, et al.
Science Translational Medicine
|
June 30, 2012
Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy
Francesco Saverio Tedesco, Mattia F M Gerli, Laura Perani, et al.
Page
of 13