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B Romero

Showing results (301-310 of 337) with videos related to

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Acta Neuropathologica|February 1, 2019
ACTN2 mutations cause "Multiple structured Core Disease" (MsCD)Xavière Lornage, Norma B Romero, Claire A Grosgogeat, et al.
Human Mutation|September 11, 2014
Mutation update: the spectra of nebulin variants and associated myopathiesVilma-Lotta Lehtokari, Kirsi Kiiski, Sarah A Sandaradura, et al.
Elife|September 14, 2016
QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver diseaseVirginia Guarani, Claude Jardel, Dominique Chrétien, et al.
Journal of Atrial Fibrillation|May 13, 2017
Atrial Fibrillation and Stroke Risk After Coronary Artery Bypass Grafting SurgeryF Hornero, E Martín, A V Mena-Durán, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Acta Neuropathologica Communications|April 15, 2014
Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotypeEdoardo Malfatti, Vilma-Lotta Lehtokari, Johann Böhm, et al.
Annals of Neurology|December 4, 2019
ASC-1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of MyopathyRocío N Villar-Quiles, Fabio Catervi, Eva Cabet, et al.
Brain : a Journal of Neurology|September 28, 2014
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutationsJohann Böhm, Valérie Biancalana, Edoardo Malfatti, et al.
Acta Neuropathologica|May 11, 2021
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusionsMridul Johari, Jaakko Sarparanta, Anna Vihola, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Pageof 34

Showing results (301-310 of 337) with videos related to

Sort By:
Pageof 34
Acta Neuropathologica|February 1, 2019
ACTN2 mutations cause "Multiple structured Core Disease" (MsCD)Xavière Lornage, Norma B Romero, Claire A Grosgogeat, et al.
Human Mutation|September 11, 2014
Mutation update: the spectra of nebulin variants and associated myopathiesVilma-Lotta Lehtokari, Kirsi Kiiski, Sarah A Sandaradura, et al.
Elife|September 14, 2016
QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver diseaseVirginia Guarani, Claude Jardel, Dominique Chrétien, et al.
Journal of Atrial Fibrillation|May 13, 2017
Atrial Fibrillation and Stroke Risk After Coronary Artery Bypass Grafting SurgeryF Hornero, E Martín, A V Mena-Durán, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Acta Neuropathologica Communications|April 15, 2014
Muscle histopathology in nebulin-related nemaline myopathy: ultrastrastructural findings correlated to disease severity and genotypeEdoardo Malfatti, Vilma-Lotta Lehtokari, Johann Böhm, et al.
Annals of Neurology|December 4, 2019
ASC-1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of MyopathyRocío N Villar-Quiles, Fabio Catervi, Eva Cabet, et al.
Brain : a Journal of Neurology|September 28, 2014
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutationsJohann Böhm, Valérie Biancalana, Edoardo Malfatti, et al.
Acta Neuropathologica|May 11, 2021
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusionsMridul Johari, Jaakko Sarparanta, Anna Vihola, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Pageof 34