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European Journal of Human Genetics : EJHG
|
April 19, 2019
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2
Alessia Peretti, Maud Perie, Didier Vincent, et al.
Annals of Clinical and Translational Neurology
|
March 19, 2026
Cracking the Code: Genotype-Phenotype Correlation Models in Sarcoglycanopathies
Leonela Luce, Goknur Selen Kocak, José Verdú-Díaz, et al.
Frontiers in Pharmacology
|
June 13, 2022
Correlation of Dyslipidemia and Inflammation With Obstructive Sleep Apnea Severity
Viseslav Popadic, Milica Brajkovic, Slobodan Klasnja, et al.
Biochemical Pharmacology
|
May 31, 2021
Pharmacological inhibition of fatty acid oxidation reduces atherosclerosis progression by suppression of macrophage NLRP3 inflammasome activation
Philipp J Hohensinner, Max Lenz, Patrick Haider, et al.
Nature Immunology
|
May 16, 2018
Cross-specificity of protective human antibodies against Klebsiella pneumoniae LPS O-antigen
Tim Rollenske, Valeria Szijarto, Jolanta Lukasiewicz, et al.
Iscience
|
July 14, 2025
Inhibition of dimeric SARS-CoV-2 Mpro displays positive cooperativity and a mixture of covalent and non-covalent binding
Krishna M Padmanabha Das, Jun Chen, Paul S Charifson, et al.
Journal of Neuromuscular Diseases
|
July 8, 2025
REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in France
Lamiae Grimaldi, Rocio Garcia-Uzquiano, Marta Gomez-Garcia de la Banda, et al.
Journal of Neurology
|
March 22, 2024
Phenotype variability and natural history of X-linked myopathy with excessive autophagy
Gorka Fernández-Eulate, Girolamo Alfieri, Marco Spinazzi, et al.
International Journal of Molecular Sciences
|
December 17, 2024
Congenital Titinopathies Linked to Mutations in <i>TTN</i> Metatranscript-Only Exons
Aurélien Perrin, Rocio Garcia-Uzquiano, Tanya Stojkovic, et al.
Neuromuscular Disorders : NMD
|
November 13, 2025
Novel missense variants associated with GNE myopathy
Johanna Ranta-Aho, Viviana Cetrangolo, Luca Bello, et al.
Page
of 107
Search research articles
Search
Showing results (911-920 of 1,067) with videos related to
Sort By:
Page
of 107
European Journal of Human Genetics : EJHG
|
April 19, 2019
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2
Alessia Peretti, Maud Perie, Didier Vincent, et al.
Annals of Clinical and Translational Neurology
|
March 19, 2026
Cracking the Code: Genotype-Phenotype Correlation Models in Sarcoglycanopathies
Leonela Luce, Goknur Selen Kocak, José Verdú-Díaz, et al.
Frontiers in Pharmacology
|
June 13, 2022
Correlation of Dyslipidemia and Inflammation With Obstructive Sleep Apnea Severity
Viseslav Popadic, Milica Brajkovic, Slobodan Klasnja, et al.
Biochemical Pharmacology
|
May 31, 2021
Pharmacological inhibition of fatty acid oxidation reduces atherosclerosis progression by suppression of macrophage NLRP3 inflammasome activation
Philipp J Hohensinner, Max Lenz, Patrick Haider, et al.
Nature Immunology
|
May 16, 2018
Cross-specificity of protective human antibodies against Klebsiella pneumoniae LPS O-antigen
Tim Rollenske, Valeria Szijarto, Jolanta Lukasiewicz, et al.
Iscience
|
July 14, 2025
Inhibition of dimeric SARS-CoV-2 Mpro displays positive cooperativity and a mixture of covalent and non-covalent binding
Krishna M Padmanabha Das, Jun Chen, Paul S Charifson, et al.
Journal of Neuromuscular Diseases
|
July 8, 2025
REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in France
Lamiae Grimaldi, Rocio Garcia-Uzquiano, Marta Gomez-Garcia de la Banda, et al.
Journal of Neurology
|
March 22, 2024
Phenotype variability and natural history of X-linked myopathy with excessive autophagy
Gorka Fernández-Eulate, Girolamo Alfieri, Marco Spinazzi, et al.
International Journal of Molecular Sciences
|
December 17, 2024
Congenital Titinopathies Linked to Mutations in <i>TTN</i> Metatranscript-Only Exons
Aurélien Perrin, Rocio Garcia-Uzquiano, Tanya Stojkovic, et al.
Neuromuscular Disorders : NMD
|
November 13, 2025
Novel missense variants associated with GNE myopathy
Johanna Ranta-Aho, Viviana Cetrangolo, Luca Bello, et al.
Page
of 107