Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Salmo Raskin

Showing results (51-60 of 112) with videos related to

Pageof 12
Sort By:
Archives of Neurology|April 11, 2007
Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10Salmo Raskin, Tetsuo Ashizawa, Hélio A G Teive, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|October 22, 2019
Neuroradiological Findings in the Spinocerebellar AtaxiasAlex Tiburtino Meira, Walter Oleschko Arruda, Sergio Eiji Ono, et al.
Arquivos De Neuro-Psiquiatria|July 30, 2015
Spinocerebellar ataxia type 10 in the South of Brazil: the Amerindian-Belgian connectionHélio Afonso Ghizoni Teive, Adriana Moro, Mariana Moscovich, et al.
BMC Medical Genetics|November 8, 2017
Phenotypic and genotypic aspects of Townes-Brock syndrome: case report of patient in southern Brazil with a new SALL1 hotspot region nonsense mutationPaulo Breno Noronha Liberalesso, Mara L Cordeiro, Simone Carreiro Vieira Karuta, et al.
Clinical Neurology and Neurosurgery|July 20, 2019
Spinocerebellar ataxias in Southern Brazil: Genotypic and phenotypic evaluation of 213 familiesFábio A Nascimento, Vinícius O R Rodrigues, Fernando C Pelloso, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2007
The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twinsRenato P Munhoz, Yosuke Wakutani, Connie Marras, et al.
Investigative Ophthalmology & Visual Science|November 13, 2025
Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological PhenotypeLinda M Reis, James Bellingham, Fabiana Louise Motta, et al.
Acta Neurologica Scandinavica|November 30, 2020
Balance and physical functioning in Spinocerebellar ataxias 3 and 10Katia M Konno, Marise Bueno Zonta, Ana T B Guimarães, et al.
Cerebellum (London, England)|December 18, 2017
Different Cerebellar Ataxia Phenotypes Associated with Mutations of the PNPLA6 Gene in Brazilian Patients with Recessive AtaxiasHélio Afonso Ghizoni Teive, Carlos Henrique F Camargo, Mario Teruo Sato, et al.
Revista Do Hospital Das Clinicas|December 11, 2003
Cystic fibrosis with normal sweat chloride concentration--case reportLuiz Vicente Ferreira da Silva Filho, Maria Helena de Carvalho Ferreira Bussamra, Cleyde Miriam Aversa Nakaie, et al.
Pageof 12

Showing results (51-60 of 112) with videos related to

Sort By:
Pageof 12
Archives of Neurology|April 11, 2007
Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10Salmo Raskin, Tetsuo Ashizawa, Hélio A G Teive, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|October 22, 2019
Neuroradiological Findings in the Spinocerebellar AtaxiasAlex Tiburtino Meira, Walter Oleschko Arruda, Sergio Eiji Ono, et al.
Arquivos De Neuro-Psiquiatria|July 30, 2015
Spinocerebellar ataxia type 10 in the South of Brazil: the Amerindian-Belgian connectionHélio Afonso Ghizoni Teive, Adriana Moro, Mariana Moscovich, et al.
BMC Medical Genetics|November 8, 2017
Phenotypic and genotypic aspects of Townes-Brock syndrome: case report of patient in southern Brazil with a new SALL1 hotspot region nonsense mutationPaulo Breno Noronha Liberalesso, Mara L Cordeiro, Simone Carreiro Vieira Karuta, et al.
Clinical Neurology and Neurosurgery|July 20, 2019
Spinocerebellar ataxias in Southern Brazil: Genotypic and phenotypic evaluation of 213 familiesFábio A Nascimento, Vinícius O R Rodrigues, Fernando C Pelloso, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2007
The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twinsRenato P Munhoz, Yosuke Wakutani, Connie Marras, et al.
Investigative Ophthalmology & Visual Science|November 13, 2025
Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological PhenotypeLinda M Reis, James Bellingham, Fabiana Louise Motta, et al.
Acta Neurologica Scandinavica|November 30, 2020
Balance and physical functioning in Spinocerebellar ataxias 3 and 10Katia M Konno, Marise Bueno Zonta, Ana T B Guimarães, et al.
Cerebellum (London, England)|December 18, 2017
Different Cerebellar Ataxia Phenotypes Associated with Mutations of the PNPLA6 Gene in Brazilian Patients with Recessive AtaxiasHélio Afonso Ghizoni Teive, Carlos Henrique F Camargo, Mario Teruo Sato, et al.
Revista Do Hospital Das Clinicas|December 11, 2003
Cystic fibrosis with normal sweat chloride concentration--case reportLuiz Vicente Ferreira da Silva Filho, Maria Helena de Carvalho Ferreira Bussamra, Cleyde Miriam Aversa Nakaie, et al.
Pageof 12