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Salmo Raskin

Showing results (41-50 of 112) with videos related to

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American Journal of Medical Genetics. Part A|August 5, 2011
Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: a locus associated with Asperger syndrome?Fabio Rueda Faucz, Josiane Souza, Aguinaldo Bonalumi Filho, et al.
Cerebellum (London, England)|September 29, 2018
Abnormal Findings in Polysomnographic Recordings of Patients with Spinocerebellar Ataxia Type 2 (SCA2)Alessandra Zanatta, Carlos Henrique Ferreira Camargo, Francisco Manoel Branco Germiniani, et al.
Cerebellum (London, England)|June 8, 2017
Nonmotor Symptoms in Patients with Spinocerebellar Ataxia Type 10Adriana Moro, Renato P Munhoz, Mariana Moscovich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 4, 2005
Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus)Renato P Munhoz, Toshitaka Kawarai, Helio A Teive, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|May 10, 2013
Diastrophic dysplasia: prenatal diagnosis and review of the literatureJonathan Celli Honório, Rafael Frederico Bruns, Luciana Fernandes Gründtner, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Global genetic variation at nine short tandem repeat loci and implications on forensic geneticsGuangyun Sun, Stephen T McGarvey, Riad Bayoumi, et al.
Arquivos De Neuro-Psiquiatria|March 8, 2014
Cervical dystonia: about familial and sporadic cases in 88 patientsCarlos Henrique F Camargo, Sarah Teixeira Camargos, Nilson Becker, et al.
Journal of Sleep Research|April 7, 2018
Sleep disorders in spinocerebellar ataxia type 10Ester London, Carlos H F Camargo, Alessandra Zanatta, et al.
Clinical Genetics|June 21, 2025
Highly Variable Expressivity of a CNV Deletion Involving TBX4 in Three Deceased Siblings With Lung Developmental Disorder and Their Mildly Affected Mother and GrandfatherPrzemyslaw Szafranski, Tomasz Gambin, Michal Kadlof, et al.
Parkinsonism & Related Disorders|December 25, 2023
Unraveling the genetic landscape of undiagnosed cerebellar ataxia in Brazilian patientsLuiz Eduardo Novis, Shahryar Alavi, David Pellerin, et al.
Pageof 12

Showing results (41-50 of 112) with videos related to

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Pageof 12
American Journal of Medical Genetics. Part A|August 5, 2011
Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: a locus associated with Asperger syndrome?Fabio Rueda Faucz, Josiane Souza, Aguinaldo Bonalumi Filho, et al.
Cerebellum (London, England)|September 29, 2018
Abnormal Findings in Polysomnographic Recordings of Patients with Spinocerebellar Ataxia Type 2 (SCA2)Alessandra Zanatta, Carlos Henrique Ferreira Camargo, Francisco Manoel Branco Germiniani, et al.
Cerebellum (London, England)|June 8, 2017
Nonmotor Symptoms in Patients with Spinocerebellar Ataxia Type 10Adriana Moro, Renato P Munhoz, Mariana Moscovich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 4, 2005
Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus)Renato P Munhoz, Toshitaka Kawarai, Helio A Teive, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|May 10, 2013
Diastrophic dysplasia: prenatal diagnosis and review of the literatureJonathan Celli Honório, Rafael Frederico Bruns, Luciana Fernandes Gründtner, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Global genetic variation at nine short tandem repeat loci and implications on forensic geneticsGuangyun Sun, Stephen T McGarvey, Riad Bayoumi, et al.
Arquivos De Neuro-Psiquiatria|March 8, 2014
Cervical dystonia: about familial and sporadic cases in 88 patientsCarlos Henrique F Camargo, Sarah Teixeira Camargos, Nilson Becker, et al.
Journal of Sleep Research|April 7, 2018
Sleep disorders in spinocerebellar ataxia type 10Ester London, Carlos H F Camargo, Alessandra Zanatta, et al.
Clinical Genetics|June 21, 2025
Highly Variable Expressivity of a CNV Deletion Involving TBX4 in Three Deceased Siblings With Lung Developmental Disorder and Their Mildly Affected Mother and GrandfatherPrzemyslaw Szafranski, Tomasz Gambin, Michal Kadlof, et al.
Parkinsonism & Related Disorders|December 25, 2023
Unraveling the genetic landscape of undiagnosed cerebellar ataxia in Brazilian patientsLuiz Eduardo Novis, Shahryar Alavi, David Pellerin, et al.
Pageof 12