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Edmar Zanoteli

Showing results (11-20 of 157) with videos related to

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Plos One|October 30, 2014
Integrative data mining highlights candidate genes for monogenic myopathiesOsorio Abath Neto, Olivier Tassy, Valérie Biancalana, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|September 11, 2002
Temporomandibular joint and masticatory muscle involvement in myotonic dystrophy: a study by magnetic resonance imagingEdmar Zanoteli, Helio K Yamashita, Hideo Suzuki, et al.
Orphanet Journal of Rare Diseases|May 6, 2025
Global variations in diagnostic methods and epidemiological estimates in Pompe disease: findings from a scoping reviewRoberto Giugliani, Faryn Solomon, Hani Kushlaf, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 25, 2026
Neurocognitive and autism spectrum profiles associated with dystrophin isoform disruption in childhood dystrophinopathies: insights from a Brazilian cohortMarco Antônio Veloso Albuquerque, Sarah Leonardo Dias, Karla Danielle Lima, et al.
BMC Neurology|March 26, 2011
Evaluation of muscle strength and motor abilities in children with type II and III spinal muscle atrophy treated with valproic acidIllora A Darbar, Paulo G Plaggert, Maria Bernadete D Resende, et al.
Arquivos De Neuro-Psiquiatria|July 6, 2004
[Normal pattern of intraepidermal nerve fibers in 30 healthy volunteers with PGP 9.5]Luciana Moura, Acary Souza Bulle Oliveira, Edmar Zanoteli, et al.
Arquivos De Neuro-Psiquiatria|May 4, 2004
[Progressive muscular atrophy: clinical and laboratory study in eleven patients]Maria Elisabeth Matta de Rezende Ferraz, Edmar Zanoteli, Acary Souza Bulle Oliveira, et al.
Journal of Neuromuscular Diseases|May 21, 2025
Patient and caregiver spinal muscular atrophy treatment attribute preferences in Latin AmericaVictoria Saenz, Marijana Chlistalla, Nayara Carlos, et al.
Arquivos De Neuro-Psiquiatria|August 2, 2005
[Analysis of the expression of collagen VI in congenital muscular dystrophy]Regina Toni Loureiro de Freitas, Edmar Zanoteli, Maria da Penha Ananias Morita, et al.
Arquivos De Neuro-Psiquiatria|March 2, 2011
Duchenne muscular dystrophy: quality of life among 95 patients evaluated using the Life Satisfaction Index for AdolescentsValdecir A Simon, Maria Bernardete Dutra Resende, Margarete A V P Simon, et al.
Pageof 16

Showing results (11-20 of 157) with videos related to

Sort By:
Pageof 16
Plos One|October 30, 2014
Integrative data mining highlights candidate genes for monogenic myopathiesOsorio Abath Neto, Olivier Tassy, Valérie Biancalana, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|September 11, 2002
Temporomandibular joint and masticatory muscle involvement in myotonic dystrophy: a study by magnetic resonance imagingEdmar Zanoteli, Helio K Yamashita, Hideo Suzuki, et al.
Orphanet Journal of Rare Diseases|May 6, 2025
Global variations in diagnostic methods and epidemiological estimates in Pompe disease: findings from a scoping reviewRoberto Giugliani, Faryn Solomon, Hani Kushlaf, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 25, 2026
Neurocognitive and autism spectrum profiles associated with dystrophin isoform disruption in childhood dystrophinopathies: insights from a Brazilian cohortMarco Antônio Veloso Albuquerque, Sarah Leonardo Dias, Karla Danielle Lima, et al.
BMC Neurology|March 26, 2011
Evaluation of muscle strength and motor abilities in children with type II and III spinal muscle atrophy treated with valproic acidIllora A Darbar, Paulo G Plaggert, Maria Bernadete D Resende, et al.
Arquivos De Neuro-Psiquiatria|July 6, 2004
[Normal pattern of intraepidermal nerve fibers in 30 healthy volunteers with PGP 9.5]Luciana Moura, Acary Souza Bulle Oliveira, Edmar Zanoteli, et al.
Arquivos De Neuro-Psiquiatria|May 4, 2004
[Progressive muscular atrophy: clinical and laboratory study in eleven patients]Maria Elisabeth Matta de Rezende Ferraz, Edmar Zanoteli, Acary Souza Bulle Oliveira, et al.
Journal of Neuromuscular Diseases|May 21, 2025
Patient and caregiver spinal muscular atrophy treatment attribute preferences in Latin AmericaVictoria Saenz, Marijana Chlistalla, Nayara Carlos, et al.
Arquivos De Neuro-Psiquiatria|August 2, 2005
[Analysis of the expression of collagen VI in congenital muscular dystrophy]Regina Toni Loureiro de Freitas, Edmar Zanoteli, Maria da Penha Ananias Morita, et al.
Arquivos De Neuro-Psiquiatria|March 2, 2011
Duchenne muscular dystrophy: quality of life among 95 patients evaluated using the Life Satisfaction Index for AdolescentsValdecir A Simon, Maria Bernardete Dutra Resende, Margarete A V P Simon, et al.
Pageof 16