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Salmo Raskin

Showing results (21-30 of 112) with videos related to

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Arquivos De Neuro-Psiquiatria|September 25, 2014
Spinocerebellar ataxia type 3: subphenotypes in a cohort of Brazilian patientsAdriana Moro, Renato P Munhoz, Walter O Arruda, et al.
American Journal of Medical Genetics. Part A|July 11, 2013
A compound heterozygote SLC26A2 mutation resulting in robin sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters. A new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasiaRoseli Maria Zechi-Ceide, Priscila Padilha Moura, Salmo Raskin, et al.
Anais Brasileiros De Dermatologia|December 15, 2010
Cutis laxa: case reportGisele Moro do Nascimento, Caroline Sampaio Alves Nunes, Paula Fatuch Menegotto, et al.
Arquivos De Neuro-Psiquiatria|October 23, 2014
Genetic evaluation for TOR1-A (DYT1) in Brazilian patients with dystoniaCarlos Henrique F Camargo, Sarah Teixeira Camargos, Salmo Raskin, et al.
Parkinsonism & Related Disorders|May 3, 2011
Spinocerebellar ataxia type 10 - A reviewHélio A G Teive, Renato P Munhoz, Walter O Arruda, et al.
Case Reports in Psychiatry|December 5, 2017
Deletion Involving the 7q31-32 Band at the CADPS2 Gene Locus in a Patient with Autism Spectrum Disorder and Recurrent Psychotic Syndrome Triggered by StressPaulo André Pera Grabowski, Alexandre Ferreira Bello, Diogo Lima Rodrigues, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 24, 2014
DYT6 in Brazil: Genetic Assessment and Clinical Characteristics of PatientsCarlos Henrique F Camargo, Sarah Teixeira Camargos, Salmo Raskin, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Application of genetic testing to define the surgical approach in a sporadic case of multiple endocrine neoplasia type 1Cesar Luiz Boguszewski, Leila Caroline Bianchet, Salmo Raskin, et al.
Journal of the Neurological Sciences|June 9, 2015
Ataxia-telangiectasia - A historical review and a proposal for a new designation: ATM syndromeHélio A G Teive, Adriana Moro, Mariana Moscovich, et al.
Human Biology|October 7, 2003
CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patients from São Paulo State, BrazilEny Maria Goloni-Bertollo, Andréa Regina B Rossit, João Batista Salomão Junior, et al.
Pageof 12

Showing results (21-30 of 112) with videos related to

Sort By:
Pageof 12
Arquivos De Neuro-Psiquiatria|September 25, 2014
Spinocerebellar ataxia type 3: subphenotypes in a cohort of Brazilian patientsAdriana Moro, Renato P Munhoz, Walter O Arruda, et al.
American Journal of Medical Genetics. Part A|July 11, 2013
A compound heterozygote SLC26A2 mutation resulting in robin sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters. A new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasiaRoseli Maria Zechi-Ceide, Priscila Padilha Moura, Salmo Raskin, et al.
Anais Brasileiros De Dermatologia|December 15, 2010
Cutis laxa: case reportGisele Moro do Nascimento, Caroline Sampaio Alves Nunes, Paula Fatuch Menegotto, et al.
Arquivos De Neuro-Psiquiatria|October 23, 2014
Genetic evaluation for TOR1-A (DYT1) in Brazilian patients with dystoniaCarlos Henrique F Camargo, Sarah Teixeira Camargos, Salmo Raskin, et al.
Parkinsonism & Related Disorders|May 3, 2011
Spinocerebellar ataxia type 10 - A reviewHélio A G Teive, Renato P Munhoz, Walter O Arruda, et al.
Case Reports in Psychiatry|December 5, 2017
Deletion Involving the 7q31-32 Band at the CADPS2 Gene Locus in a Patient with Autism Spectrum Disorder and Recurrent Psychotic Syndrome Triggered by StressPaulo André Pera Grabowski, Alexandre Ferreira Bello, Diogo Lima Rodrigues, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 24, 2014
DYT6 in Brazil: Genetic Assessment and Clinical Characteristics of PatientsCarlos Henrique F Camargo, Sarah Teixeira Camargos, Salmo Raskin, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Application of genetic testing to define the surgical approach in a sporadic case of multiple endocrine neoplasia type 1Cesar Luiz Boguszewski, Leila Caroline Bianchet, Salmo Raskin, et al.
Journal of the Neurological Sciences|June 9, 2015
Ataxia-telangiectasia - A historical review and a proposal for a new designation: ATM syndromeHélio A G Teive, Adriana Moro, Mariana Moscovich, et al.
Human Biology|October 7, 2003
CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patients from São Paulo State, BrazilEny Maria Goloni-Bertollo, Andréa Regina B Rossit, João Batista Salomão Junior, et al.
Pageof 12