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B Romero

Showing results (211-220 of 337) with videos related to

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Frontiers in Neurology|October 23, 2019
Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic VariantsAriadna González-Del Angel, Michela Bisciglia, Steven Vargas-Cañas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2014
Autosomal dominant eccentric core disease caused by a heterozygous mutation in the MYH7 geneNorma B Romero, Ting Xie, Edoardo Malfatti, et al.
Neuromuscular Disorders : NMD|August 17, 2016
Mild clinical presentation in KLHL40-related nemaline myopathy (NEM 8)Andreea M Seferian, Edoardo Malfatti, Caroline Bosson, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
BMC Veterinary Research|January 28, 2022
Effect of the topical administration of corticosteroids and tuberculin pre-sensitisation on the diagnosis of tuberculosis in goatsJ Ortega, A Roy, A Díaz-Castillo, et al.
Molecular Therapy. Nucleic Acids|July 29, 2024
Functional benefit of CRISPR-Cas9-induced allele deletion for <i>RYR1</i> dominant mutationMathilde Beaufils, Margaux Melka, Julie Brocard, et al.
Gates Open Research|January 25, 2022
Testing for sensory threshold in drinking water with added calcium: a first step towards developing a calcium fortified waterGabriela Cormick, Natalia Matamoros, Iris B Romero, et al.
Neurology|July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutationA Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
Neuromuscular Disorders : NMD|October 13, 2012
Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositisJulia V Wanschitz, Odile Dubourg, Emmanuelle Lacene, et al.
Journal of Neuropathology and Experimental Neurology|July 2, 2020
A Heterozygous Mutation in the Filamin C Gene Causes an Unusual Nemaline Myopathy With Ring FibersTeresinha Evangelista, Xavière Lornage, Pierre G Carlier, et al.
Pageof 34

Showing results (211-220 of 337) with videos related to

Sort By:
Pageof 34
Frontiers in Neurology|October 23, 2019
Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic VariantsAriadna González-Del Angel, Michela Bisciglia, Steven Vargas-Cañas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2014
Autosomal dominant eccentric core disease caused by a heterozygous mutation in the MYH7 geneNorma B Romero, Ting Xie, Edoardo Malfatti, et al.
Neuromuscular Disorders : NMD|August 17, 2016
Mild clinical presentation in KLHL40-related nemaline myopathy (NEM 8)Andreea M Seferian, Edoardo Malfatti, Caroline Bosson, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
BMC Veterinary Research|January 28, 2022
Effect of the topical administration of corticosteroids and tuberculin pre-sensitisation on the diagnosis of tuberculosis in goatsJ Ortega, A Roy, A Díaz-Castillo, et al.
Molecular Therapy. Nucleic Acids|July 29, 2024
Functional benefit of CRISPR-Cas9-induced allele deletion for <i>RYR1</i> dominant mutationMathilde Beaufils, Margaux Melka, Julie Brocard, et al.
Gates Open Research|January 25, 2022
Testing for sensory threshold in drinking water with added calcium: a first step towards developing a calcium fortified waterGabriela Cormick, Natalia Matamoros, Iris B Romero, et al.
Neurology|July 20, 2007
New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutationA Yanagisawa, C Bouchet, P Y K Van den Bergh, et al.
Neuromuscular Disorders : NMD|October 13, 2012
Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositisJulia V Wanschitz, Odile Dubourg, Emmanuelle Lacene, et al.
Journal of Neuropathology and Experimental Neurology|July 2, 2020
A Heterozygous Mutation in the Filamin C Gene Causes an Unusual Nemaline Myopathy With Ring FibersTeresinha Evangelista, Xavière Lornage, Pierre G Carlier, et al.
Pageof 34