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Alejandro Horga

Showing results (11-20 of 39) with videos related to

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Journal of Neurology|March 17, 2026
Targeted neurological screening for RFC1-related disease in unexplained chronic coughVicente Gajate-García, María Fenollar-Cortés, Juan Luis Rodríguez-Hermosa, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 22, 2022
Tardive myoclonic focal seizures after electroconvulsive therapy, lithium and bupropion treatmentPablo Mayo Rodríguez, Ana Fernández Revuelta, María Romeral Jiménez, et al.
Journal of Neurology|July 22, 2015
Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathiesAlejandro Horga, Ellen Cottenie, Pedro J Tomaselli, et al.
Revista De Neurologia|July 21, 2010
[Demyelinating lesions as incidental findings in magnetic resonance imaging: a study of 11 cases with clinico-radiological follow-up and a review of the literature]Alba Sierra-Marcos, Raquel Mitjana, Joaquín Castilló, et al.
Neurology|September 16, 2016
SIGMAR1 mutation associated with autosomal recessive Silver-like syndromeAlejandro Horga, Pedro J Tomaselli, Michael A Gonzalez, et al.
Neurology|March 22, 2013
Prevalence study of genetically defined skeletal muscle channelopathies in EnglandAlejandro Horga, Dipa L Raja Rayan, Emma Matthews, et al.
Neurology. Genetics|April 28, 2020
Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA<sup>Gly</sup> (<i>MT-TG</i>) variantOlivia V Poole, Alejandro Horga, Steven A Hardy, et al.
Neurology|March 12, 2017
Mutations in noncoding regions of <i>GJB1</i> are a major cause of X-linked CMTPedro J Tomaselli, Alexander M Rossor, Alejandro Horga, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 16, 2013
Early brain pseudoatrophy while on natalizumab therapy is due to white matter volume changesAngela Vidal-Jordana, Jaume Sastre-Garriga, Francisco Pérez-Miralles, et al.
Brain : a Journal of Neurology|October 5, 2014
Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegiaAlejandro Horga, Robert D S Pitceathly, Julian C Blake, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Journal of Neurology|March 17, 2026
Targeted neurological screening for RFC1-related disease in unexplained chronic coughVicente Gajate-García, María Fenollar-Cortés, Juan Luis Rodríguez-Hermosa, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 22, 2022
Tardive myoclonic focal seizures after electroconvulsive therapy, lithium and bupropion treatmentPablo Mayo Rodríguez, Ana Fernández Revuelta, María Romeral Jiménez, et al.
Journal of Neurology|July 22, 2015
Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathiesAlejandro Horga, Ellen Cottenie, Pedro J Tomaselli, et al.
Revista De Neurologia|July 21, 2010
[Demyelinating lesions as incidental findings in magnetic resonance imaging: a study of 11 cases with clinico-radiological follow-up and a review of the literature]Alba Sierra-Marcos, Raquel Mitjana, Joaquín Castilló, et al.
Neurology|September 16, 2016
SIGMAR1 mutation associated with autosomal recessive Silver-like syndromeAlejandro Horga, Pedro J Tomaselli, Michael A Gonzalez, et al.
Neurology|March 22, 2013
Prevalence study of genetically defined skeletal muscle channelopathies in EnglandAlejandro Horga, Dipa L Raja Rayan, Emma Matthews, et al.
Neurology. Genetics|April 28, 2020
Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA<sup>Gly</sup> (<i>MT-TG</i>) variantOlivia V Poole, Alejandro Horga, Steven A Hardy, et al.
Neurology|March 12, 2017
Mutations in noncoding regions of <i>GJB1</i> are a major cause of X-linked CMTPedro J Tomaselli, Alexander M Rossor, Alejandro Horga, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 16, 2013
Early brain pseudoatrophy while on natalizumab therapy is due to white matter volume changesAngela Vidal-Jordana, Jaume Sastre-Garriga, Francisco Pérez-Miralles, et al.
Brain : a Journal of Neurology|October 5, 2014
Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegiaAlejandro Horga, Robert D S Pitceathly, Julian C Blake, et al.
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