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Andoni Urtizberea

Showing results (11-20 of 87) with videos related to

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Journal of Child Neurology|July 31, 2003
Evoked potentials in spinal muscular atrophyFawzia Cheliout-Heraut, Annie Barois, Andoni Urtizberea, et al.
Revue Neurologique|May 4, 2012
Recommendations for the management of facioscapulohumeral muscular dystrophy in 2011S Attarian, E Salort-Campana, K Nguyen, et al.
Neurology India|January 21, 2014
New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac diseaseAtchayaram Nalini, Narayanappa Gayathri, Pascale Richard, et al.
Neurology India|November 1, 2008
DysferlinopathiesJ Andoni Urtizberea, Guillaume Bassez, France Leturcq, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicineJ Andoni Urtizberea, Qi Shi Fan, Elizabeth Vroom, et al.
Neurology India|September 23, 2009
Spectrum of mutations in sarcoglycan genes in the Mumbai region of western India: high prevalence of 525del TSatish V Khadilkar, Rakesh K Singh, Madhuri Hegde, et al.
Iranian Journal of Child Neurology|February 9, 2021
Novel Homozygous Pathogenic Mutations of LAMA 2 Gene in Patients with Congen ital Muscular DystrophyNegar Khodaenia, Zahra Farjami, Amir Hosein Ashnaei, et al.
Indian Journal of Pediatrics|April 2, 2010
Mutation studies in X-linked myotubular myopathy in three Indian familiesSunita Bijarnia, Ratna D Puri, Monika Jain, et al.
Journal of the Neurological Sciences|December 17, 2015
Dysferlinopathy in Iran: Clinical and genetic reportFarzad Fatehi, Shahriar Nafissi, J Andoni Urtizberea, et al.
Journal of Neuromuscular Diseases|August 20, 2025
Recurrent nonsense p.Trp3416* variant in the <i>DMD</i> gene identified in healthy Lebanese individuals: Implications for variant classification and genotype-phenotype correlationsEliane Chouery, Cybel Mehawej, Serena Youssef, et al.
Pageof 9

Showing results (11-20 of 87) with videos related to

Sort By:
Pageof 9
Journal of Child Neurology|July 31, 2003
Evoked potentials in spinal muscular atrophyFawzia Cheliout-Heraut, Annie Barois, Andoni Urtizberea, et al.
Revue Neurologique|May 4, 2012
Recommendations for the management of facioscapulohumeral muscular dystrophy in 2011S Attarian, E Salort-Campana, K Nguyen, et al.
Neurology India|January 21, 2014
New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac diseaseAtchayaram Nalini, Narayanappa Gayathri, Pascale Richard, et al.
Neurology India|November 1, 2008
DysferlinopathiesJ Andoni Urtizberea, Guillaume Bassez, France Leturcq, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicineJ Andoni Urtizberea, Qi Shi Fan, Elizabeth Vroom, et al.
Neurology India|September 23, 2009
Spectrum of mutations in sarcoglycan genes in the Mumbai region of western India: high prevalence of 525del TSatish V Khadilkar, Rakesh K Singh, Madhuri Hegde, et al.
Iranian Journal of Child Neurology|February 9, 2021
Novel Homozygous Pathogenic Mutations of LAMA 2 Gene in Patients with Congen ital Muscular DystrophyNegar Khodaenia, Zahra Farjami, Amir Hosein Ashnaei, et al.
Indian Journal of Pediatrics|April 2, 2010
Mutation studies in X-linked myotubular myopathy in three Indian familiesSunita Bijarnia, Ratna D Puri, Monika Jain, et al.
Journal of the Neurological Sciences|December 17, 2015
Dysferlinopathy in Iran: Clinical and genetic reportFarzad Fatehi, Shahriar Nafissi, J Andoni Urtizberea, et al.
Journal of Neuromuscular Diseases|August 20, 2025
Recurrent nonsense p.Trp3416* variant in the <i>DMD</i> gene identified in healthy Lebanese individuals: Implications for variant classification and genotype-phenotype correlationsEliane Chouery, Cybel Mehawej, Serena Youssef, et al.
Pageof 9