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Showing results (291-300 of 337) with videos related to

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Journal of Neuropathology and Experimental Neurology|March 11, 2021
NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein MaterialKarlijn Bouman, Benno Küsters, Josine M De Winter, et al.
Annals of Neurology|December 26, 2006
Nemaline myopathy caused by absence of alpha-skeletal muscle actinKristen J Nowak, Caroline A Sewry, Carmen Navarro, et al.
Annals of Neurology|April 12, 2006
CAPN3 mutations in patients with idiopathic eosinophilic myositisMartin Krahn, Adolfo Lopez de Munain, Nathalie Streichenberger, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
American Journal of Human Genetics|September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophyLucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
JCI Insight|October 3, 2023
Human skeletal myopathy myosin mutations disrupt myosin head sequestrationGlenn Carrington, Abbi Hau, Sarah Kosta, et al.
The New England Journal of Medicine|April 2, 2025
A Phase 3 Trial of Upadacitinib for Giant-Cell ArteritisDaniel Blockmans, Sara K Penn, Arathi R Setty, et al.
American Journal of Human Genetics|January 22, 2013
Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathyJohann Böhm, Frédéric Chevessier, André Maues De Paula, et al.
Annals of Neurology|January 13, 2018
Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3)Barbara Joureau, Josine Marieke de Winter, Stefan Conijn, et al.
BMJ Open|October 5, 2023
Mental health data available in representative surveys conducted in Latin America and the Caribbean countries: a scoping reviewFrancesca Ramírez-Bontá, Rafaela Vásquez-Vílchez, Milagros Cabrera-Alva, et al.
Pageof 34

Showing results (291-300 of 337) with videos related to

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Pageof 34
Journal of Neuropathology and Experimental Neurology|March 11, 2021
NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein MaterialKarlijn Bouman, Benno Küsters, Josine M De Winter, et al.
Annals of Neurology|December 26, 2006
Nemaline myopathy caused by absence of alpha-skeletal muscle actinKristen J Nowak, Caroline A Sewry, Carmen Navarro, et al.
Annals of Neurology|April 12, 2006
CAPN3 mutations in patients with idiopathic eosinophilic myositisMartin Krahn, Adolfo Lopez de Munain, Nathalie Streichenberger, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
American Journal of Human Genetics|September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophyLucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
JCI Insight|October 3, 2023
Human skeletal myopathy myosin mutations disrupt myosin head sequestrationGlenn Carrington, Abbi Hau, Sarah Kosta, et al.
The New England Journal of Medicine|April 2, 2025
A Phase 3 Trial of Upadacitinib for Giant-Cell ArteritisDaniel Blockmans, Sara K Penn, Arathi R Setty, et al.
American Journal of Human Genetics|January 22, 2013
Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathyJohann Böhm, Frédéric Chevessier, André Maues De Paula, et al.
Annals of Neurology|January 13, 2018
Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3)Barbara Joureau, Josine Marieke de Winter, Stefan Conijn, et al.
BMJ Open|October 5, 2023
Mental health data available in representative surveys conducted in Latin America and the Caribbean countries: a scoping reviewFrancesca Ramírez-Bontá, Rafaela Vásquez-Vílchez, Milagros Cabrera-Alva, et al.
Pageof 34