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Isabel Illa

Showing results (41-50 of 136) with videos related to

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Human Mutation|May 20, 2014
Genetic and epigenetic determinants of low dysferlin expression in monocytesEduard Gallardo, Arunkanth Ankala, Yaiza Núñez-Álvarez, et al.
Proteomics. Clinical Applications|December 8, 2010
Proteomics identification of differentially expressed proteins in the muscle of dysferlin myopathy patientsCarolina De la Torre, Isabel Illa, Georgine Faulkner, et al.
Journal of Neuropathology and Experimental Neurology|May 29, 2003
Inflammatory myopathy with abundant macrophages (IMAM): a condition sharing similarities with cytophagic histiocytic panniculitis and distinct from macrophagic myofasciitisGuillaume Bassez, Francois-Jérôme Authier, Emmanuèle Lechapt-Zalcman, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
Clinical and serological features of acute sensory ataxic neuropathy with antiganglioside antibodiesRicard Rojas-García, Luis Querol, Eduard Gallardo, et al.
Mitochondrion|September 4, 2010
A novel mutation in the mitochondrial tRNA(Ala) gene (m.5636T>C) in a patient with progressive external ophthalmoplegiaTomàs Pinós, Mario Marotta, Eduard Gallardo, et al.
Annals of Clinical and Translational Neurology|May 16, 2018
Antibodies against cell adhesion molecules and neural structures in paraneoplastic neuropathiesAna M Siles, Eugenia Martínez-Hernández, Josefa Araque, et al.
Frontiers in Immunology|April 30, 2019
Caveats and Pitfalls of SOX1 Autoantibody Testing With a Commercial Line Blot Assay in Paraneoplastic Neurological InvestigationsRaquel Ruiz-García, Eugenia Martínez-Hernández, Milagros García-Ormaechea, et al.
Nature Clinical Practice. Neurology|July 6, 2007
Antibodies to AChR, MuSK and VGKC in a patient with myasthenia gravis and Morvan's syndromeJordi Díaz-Manera, Ricard Rojas-García, Eduard Gallardo, et al.
Neuromuscular Disorders : NMD|July 2, 2021
Late onset Sandhoff disease presenting with lower motor neuron disease and stutteringJorge Alonso-Pérez, Ana Casasús, Álvaro Gimenez-Muñoz, et al.
The Journal of Biological Chemistry|April 13, 2006
Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro"Noemí de Luna, Eduard Gallardo, Mario Soriano, et al.
Pageof 14

Showing results (41-50 of 136) with videos related to

Sort By:
Pageof 14
Human Mutation|May 20, 2014
Genetic and epigenetic determinants of low dysferlin expression in monocytesEduard Gallardo, Arunkanth Ankala, Yaiza Núñez-Álvarez, et al.
Proteomics. Clinical Applications|December 8, 2010
Proteomics identification of differentially expressed proteins in the muscle of dysferlin myopathy patientsCarolina De la Torre, Isabel Illa, Georgine Faulkner, et al.
Journal of Neuropathology and Experimental Neurology|May 29, 2003
Inflammatory myopathy with abundant macrophages (IMAM): a condition sharing similarities with cytophagic histiocytic panniculitis and distinct from macrophagic myofasciitisGuillaume Bassez, Francois-Jérôme Authier, Emmanuèle Lechapt-Zalcman, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
Clinical and serological features of acute sensory ataxic neuropathy with antiganglioside antibodiesRicard Rojas-García, Luis Querol, Eduard Gallardo, et al.
Mitochondrion|September 4, 2010
A novel mutation in the mitochondrial tRNA(Ala) gene (m.5636T>C) in a patient with progressive external ophthalmoplegiaTomàs Pinós, Mario Marotta, Eduard Gallardo, et al.
Annals of Clinical and Translational Neurology|May 16, 2018
Antibodies against cell adhesion molecules and neural structures in paraneoplastic neuropathiesAna M Siles, Eugenia Martínez-Hernández, Josefa Araque, et al.
Frontiers in Immunology|April 30, 2019
Caveats and Pitfalls of SOX1 Autoantibody Testing With a Commercial Line Blot Assay in Paraneoplastic Neurological InvestigationsRaquel Ruiz-García, Eugenia Martínez-Hernández, Milagros García-Ormaechea, et al.
Nature Clinical Practice. Neurology|July 6, 2007
Antibodies to AChR, MuSK and VGKC in a patient with myasthenia gravis and Morvan's syndromeJordi Díaz-Manera, Ricard Rojas-García, Eduard Gallardo, et al.
Neuromuscular Disorders : NMD|July 2, 2021
Late onset Sandhoff disease presenting with lower motor neuron disease and stutteringJorge Alonso-Pérez, Ana Casasús, Álvaro Gimenez-Muñoz, et al.
The Journal of Biological Chemistry|April 13, 2006
Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro"Noemí de Luna, Eduard Gallardo, Mario Soriano, et al.
Pageof 14