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Salmo Raskin

Showing results (11-20 of 112) with videos related to

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Mutation Research. Reviews in Mutation Research|August 18, 2020
A comprehensive analysis of AHRR gene as a candidate for cleft lip with or without cleft palateBianca Domit Werner Linnenkamp, Salmo Raskin, Selene Elifio Esposito, et al.
Arquivos De Neuro-Psiquiatria|July 30, 2020
Evidence and practices of the use of next generation sequencing in patients with undiagnosed autosomal dominant cerebellar ataxias: a reviewLuiz Eduardo Novis, Mariana Spitz, Marcia Jardim, et al.
Genetics and Molecular Biology|January 5, 2012
Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndromeJosiane Souza, Fábio Faucz, Vanessa Sotomaior, et al.
Arquivos De Neuro-Psiquiatria|July 17, 2013
Clinical relevance of "bulging eyes" for the differential diagnosis of spinocerebellar ataxiasAdriana Moro, Renato Puppi Munhoz, Walter Oleschko Arruda, et al.
Arquivos De Neuro-Psiquiatria|December 21, 2007
The history of spinocerebellar ataxia type 10 in Brazil: travels of a geneHélio A G Teive, Walter O Arruda, Salmo Raskin, et al.
Gene|March 12, 2014
A 1.5Mb terminal deletion of 12p associated with autism spectrum disorderIsabela M W Silva, Jill Rosenfeld, Sergio A Antoniuk, et al.
Arquivos De Neuro-Psiquiatria|August 1, 2007
Non-choreic movement disorders as initial manifestations of Huntington's diseaseNilson Becker, Renato P Munhoz, Salmo Raskin, et al.
American Journal of Medical Genetics. Part A|June 25, 2013
Richieri-costa and Pereira syndrome: severe phenotypeSalmo Raskin, Marcela Souza, Mariana C Medeiros, et al.
Clinics (Sao Paulo, Brazil)|August 3, 2011
Tremor in X-linked recessive spinal and bulbar muscular atrophy (Kennedy's disease)Francisco A Dias, Renato P Munhoz, Salmo Raskin, et al.
European Neurology|October 18, 2014
Movement disorders in spinocerebellar ataxias in a cohort of Brazilian patientsAdriana Moro, Renato P Munhoz, Mariana Moscovich, et al.
Pageof 12

Showing results (11-20 of 112) with videos related to

Sort By:
Pageof 12
Mutation Research. Reviews in Mutation Research|August 18, 2020
A comprehensive analysis of AHRR gene as a candidate for cleft lip with or without cleft palateBianca Domit Werner Linnenkamp, Salmo Raskin, Selene Elifio Esposito, et al.
Arquivos De Neuro-Psiquiatria|July 30, 2020
Evidence and practices of the use of next generation sequencing in patients with undiagnosed autosomal dominant cerebellar ataxias: a reviewLuiz Eduardo Novis, Mariana Spitz, Marcia Jardim, et al.
Genetics and Molecular Biology|January 5, 2012
Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndromeJosiane Souza, Fábio Faucz, Vanessa Sotomaior, et al.
Arquivos De Neuro-Psiquiatria|July 17, 2013
Clinical relevance of "bulging eyes" for the differential diagnosis of spinocerebellar ataxiasAdriana Moro, Renato Puppi Munhoz, Walter Oleschko Arruda, et al.
Arquivos De Neuro-Psiquiatria|December 21, 2007
The history of spinocerebellar ataxia type 10 in Brazil: travels of a geneHélio A G Teive, Walter O Arruda, Salmo Raskin, et al.
Gene|March 12, 2014
A 1.5Mb terminal deletion of 12p associated with autism spectrum disorderIsabela M W Silva, Jill Rosenfeld, Sergio A Antoniuk, et al.
Arquivos De Neuro-Psiquiatria|August 1, 2007
Non-choreic movement disorders as initial manifestations of Huntington's diseaseNilson Becker, Renato P Munhoz, Salmo Raskin, et al.
American Journal of Medical Genetics. Part A|June 25, 2013
Richieri-costa and Pereira syndrome: severe phenotypeSalmo Raskin, Marcela Souza, Mariana C Medeiros, et al.
Clinics (Sao Paulo, Brazil)|August 3, 2011
Tremor in X-linked recessive spinal and bulbar muscular atrophy (Kennedy's disease)Francisco A Dias, Renato P Munhoz, Salmo Raskin, et al.
European Neurology|October 18, 2014
Movement disorders in spinocerebellar ataxias in a cohort of Brazilian patientsAdriana Moro, Renato P Munhoz, Mariana Moscovich, et al.
Pageof 12