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Nutrients
|
January 8, 2025
Dietary Lipid Quantity and Quality Modulate the Postprandial Metabolomic Profile in Patients with Metabolic Syndrome
Marina Mora-Ortiz, Elena M Yubero-Serrano, Feliciano Priego-Capote, et al.
Human Molecular Genetics
|
June 14, 2014
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations
Stefania Di Costanzo, Anuradha Balasubramanian, Heather L Pond, et al.
Orphanet Journal of Rare Diseases
|
October 26, 2016
The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks
Chiara Baldo, Lorena Casareto, Alessandra Renieri, et al.
Frontiers in Physiology
|
July 26, 2021
Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the <i>mdx</i> Mouse Model and Patients
Rachele Rossi, Maria Sofia Falzarano, Hana Osman, et al.
Neuromuscular Disorders : NMD
|
March 28, 2016
Novel findings associated with MTM1 suggest a higher number of female symptomatic carriers
Marco Savarese, Olimpia Musumeci, Teresa Giugliano, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology
|
November 11, 2024
Validation of a Urine-Based Proteomics Test to Predict Clinically Significant Prostate Cancer: Complementing mpMRI Pathway
Maria Frantzi, Ana C Morillo, Guillermo Lendinez, et al.
BMC Medicine
|
October 27, 2022
Metabolomics analysis of type 2 diabetes remission identifies 12 metabolites with predictive capacity: a CORDIOPREV clinical trial study
Marina Mora-Ortiz, Juan F Alcala-Diaz, Oriol Alberto Rangel-Zuñiga, et al.
Journal of Medical Genetics
|
October 19, 2014
Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1
Johann Böhm, Frédéric Chevessier, Catherine Koch, et al.
Acta Neuropathologica Communications
|
July 25, 2015
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy
Alessandra Ruggieri, Francesco Brancati, Simona Zanotti, et al.
American Journal of Human Genetics
|
April 30, 2013
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase
Philippe M Campeau, Guy M Lenk, James T Lu, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 122) with videos related to
Sort By:
Page
of 13
Nutrients
|
January 8, 2025
Dietary Lipid Quantity and Quality Modulate the Postprandial Metabolomic Profile in Patients with Metabolic Syndrome
Marina Mora-Ortiz, Elena M Yubero-Serrano, Feliciano Priego-Capote, et al.
Human Molecular Genetics
|
June 14, 2014
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations
Stefania Di Costanzo, Anuradha Balasubramanian, Heather L Pond, et al.
Orphanet Journal of Rare Diseases
|
October 26, 2016
The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks
Chiara Baldo, Lorena Casareto, Alessandra Renieri, et al.
Frontiers in Physiology
|
July 26, 2021
Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the <i>mdx</i> Mouse Model and Patients
Rachele Rossi, Maria Sofia Falzarano, Hana Osman, et al.
Neuromuscular Disorders : NMD
|
March 28, 2016
Novel findings associated with MTM1 suggest a higher number of female symptomatic carriers
Marco Savarese, Olimpia Musumeci, Teresa Giugliano, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology
|
November 11, 2024
Validation of a Urine-Based Proteomics Test to Predict Clinically Significant Prostate Cancer: Complementing mpMRI Pathway
Maria Frantzi, Ana C Morillo, Guillermo Lendinez, et al.
BMC Medicine
|
October 27, 2022
Metabolomics analysis of type 2 diabetes remission identifies 12 metabolites with predictive capacity: a CORDIOPREV clinical trial study
Marina Mora-Ortiz, Juan F Alcala-Diaz, Oriol Alberto Rangel-Zuñiga, et al.
Journal of Medical Genetics
|
October 19, 2014
Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1
Johann Böhm, Frédéric Chevessier, Catherine Koch, et al.
Acta Neuropathologica Communications
|
July 25, 2015
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy
Alessandra Ruggieri, Francesco Brancati, Simona Zanotti, et al.
American Journal of Human Genetics
|
April 30, 2013
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase
Philippe M Campeau, Guy M Lenk, James T Lu, et al.
Page
of 13