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Antioxidants (Basel, Switzerland)
|
January 26, 2024
Telomere Maintenance Is Associated with Type 2 Diabetes Remission in Response to a Long-Term Dietary Intervention without Non-Weight Loss in Patients with Coronary Heart Disease: From the CORDIOPREV Randomized Controlled Trial
Ana Ojeda-Rodriguez, Juan F Alcala-Diaz, Oriol Alberto Rangel-Zuñiga, et al.
European Journal of Human Genetics : EJHG
|
February 4, 2018
The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers
Sabina Gainotti, Paola Torreri, Chiuhui Mary Wang, et al.
Nature Communications
|
October 1, 2024
Superior metabolic improvement of polycystic ovary syndrome traits after GLP1-based multi-agonist therapy
Miguel A Sánchez-Garrido, Víctor Serrano-López, Francisco Ruiz-Pino, et al.
Journal of Neuromuscular Diseases
|
February 11, 2020
Improved Criteria for the Classification of Titin Variants in Inherited Skeletal Myopathies
Marco Savarese, Mridul Johari, Katherine Johnson, et al.
Neurobiology of Aging
|
February 12, 2015
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis
Qiang Gang, Conceicao Bettencourt, Pedro M Machado, et al.
American Journal of Human Genetics
|
February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy
Daniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Human Mutation
|
November 13, 2007
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients
Michela Guglieri, Francesca Magri, Maria Grazia D'Angelo, et al.
Aging and Disease
|
April 24, 2019
Collagen XIX Alpha 1 Improves Prognosis in Amyotrophic Lateral Sclerosis
Ana C Calvo, Gabriela Atencia Cibreiro, Paz Torre Merino, et al.
American Journal of Human Genetics
|
September 11, 2012
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
M Chiara Manzini, Dimira E Tambunan, R Sean Hill, et al.
Neurology
|
February 6, 2015
Prevalence of congenital muscular dystrophy in Italy: a population study
Alessandra Graziano, Flaviana Bianco, Adele D'Amico, et al.
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Search research articles
Search
Showing results (101-110 of 122) with videos related to
Sort By:
Page
of 13
Antioxidants (Basel, Switzerland)
|
January 26, 2024
Telomere Maintenance Is Associated with Type 2 Diabetes Remission in Response to a Long-Term Dietary Intervention without Non-Weight Loss in Patients with Coronary Heart Disease: From the CORDIOPREV Randomized Controlled Trial
Ana Ojeda-Rodriguez, Juan F Alcala-Diaz, Oriol Alberto Rangel-Zuñiga, et al.
European Journal of Human Genetics : EJHG
|
February 4, 2018
The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers
Sabina Gainotti, Paola Torreri, Chiuhui Mary Wang, et al.
Nature Communications
|
October 1, 2024
Superior metabolic improvement of polycystic ovary syndrome traits after GLP1-based multi-agonist therapy
Miguel A Sánchez-Garrido, Víctor Serrano-López, Francisco Ruiz-Pino, et al.
Journal of Neuromuscular Diseases
|
February 11, 2020
Improved Criteria for the Classification of Titin Variants in Inherited Skeletal Myopathies
Marco Savarese, Mridul Johari, Katherine Johnson, et al.
Neurobiology of Aging
|
February 12, 2015
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis
Qiang Gang, Conceicao Bettencourt, Pedro M Machado, et al.
American Journal of Human Genetics
|
February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy
Daniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Human Mutation
|
November 13, 2007
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients
Michela Guglieri, Francesca Magri, Maria Grazia D'Angelo, et al.
Aging and Disease
|
April 24, 2019
Collagen XIX Alpha 1 Improves Prognosis in Amyotrophic Lateral Sclerosis
Ana C Calvo, Gabriela Atencia Cibreiro, Paz Torre Merino, et al.
American Journal of Human Genetics
|
September 11, 2012
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
M Chiara Manzini, Dimira E Tambunan, R Sean Hill, et al.
Neurology
|
February 6, 2015
Prevalence of congenital muscular dystrophy in Italy: a population study
Alessandra Graziano, Flaviana Bianco, Adele D'Amico, et al.
Page
of 13