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Movement Disorders : Official Journal of the Movement Disorder Society
|
April 24, 2021
Retinal Architecture in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Insights into Disease Pathogenesis and Biomarkers
Flávio Moura Rezende Filho, Fion Bremner, José Luiz Pedroso, et al.
Orphanet Journal of Rare Diseases
|
July 20, 2024
Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP)
Fábio Fernandes, Georgina Del Cisne Jadán Luzuriaga, Guilherme Wesley Peixoto da Fonseca, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 25, 2022
RFC1-Related Disorder: In Vivo Evaluation of Spinal Cord Damage
Thiago J R Rezende, Gabriel S Schmitt, Fabricio D de Lima, et al.
Brain : a Journal of Neurology
|
December 21, 2013
PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum
Matthis Synofzik, Michael A Gonzalez, Charles Marques Lourenco, et al.
Cerebellum (London, England)
|
May 6, 2021
Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective
Felipe Franco da Graça, Thiago M Peluzzo, Luciana Cardoso Bonadia, et al.
Plos Neglected Tropical Diseases
|
August 20, 2021
Innovative tracking, active search and follow-up strategies for new leprosy cases in the female prison population
Claudia Maria Lincoln Silva, Fred Bernardes Filho, Glauber Voltan, et al.
Brain Communications
|
March 18, 2024
Dominant <i>NARS1</i> mutations causing axonal Charcot-Marie-Tooth disease expand <i>NARS1</i>-associated diseases
Danique Beijer, Sheila Marte, Jiaxin C Li, et al.
Movement Disorders Clinical Practice
|
January 31, 2024
Cranial Nerve Thinning Distinguishes RFC1-Related Disorder from Other Late-Onset Ataxias
Camila C Lobo, Guilherme S O Wertheimer, Gabriel S Schmitt, et al.
Brain : a Journal of Neurology
|
October 19, 2021
Primary neural leprosy: clinical, neurophysiological and pathological presentation and progression
Pedro J Tomaselli, Diogo F Dos Santos, André C J Dos Santos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 12, 2018
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response
Ingrid Faber, Alberto Rolim Muro Martinez, Carlos Roberto Martins, et al.
Page
of 20
Search research articles
Search
Showing results (141-150 of 197) with videos related to
Sort By:
Page
of 20
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 24, 2021
Retinal Architecture in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Insights into Disease Pathogenesis and Biomarkers
Flávio Moura Rezende Filho, Fion Bremner, José Luiz Pedroso, et al.
Orphanet Journal of Rare Diseases
|
July 20, 2024
Clinical and genetic profiles of patients with hereditary and wild-type transthyretin amyloidosis: the Transthyretin Cardiac Amyloidosis Registry in the state of São Paulo, Brazil (REACT-SP)
Fábio Fernandes, Georgina Del Cisne Jadán Luzuriaga, Guilherme Wesley Peixoto da Fonseca, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 25, 2022
RFC1-Related Disorder: In Vivo Evaluation of Spinal Cord Damage
Thiago J R Rezende, Gabriel S Schmitt, Fabricio D de Lima, et al.
Brain : a Journal of Neurology
|
December 21, 2013
PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum
Matthis Synofzik, Michael A Gonzalez, Charles Marques Lourenco, et al.
Cerebellum (London, England)
|
May 6, 2021
Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective
Felipe Franco da Graça, Thiago M Peluzzo, Luciana Cardoso Bonadia, et al.
Plos Neglected Tropical Diseases
|
August 20, 2021
Innovative tracking, active search and follow-up strategies for new leprosy cases in the female prison population
Claudia Maria Lincoln Silva, Fred Bernardes Filho, Glauber Voltan, et al.
Brain Communications
|
March 18, 2024
Dominant <i>NARS1</i> mutations causing axonal Charcot-Marie-Tooth disease expand <i>NARS1</i>-associated diseases
Danique Beijer, Sheila Marte, Jiaxin C Li, et al.
Movement Disorders Clinical Practice
|
January 31, 2024
Cranial Nerve Thinning Distinguishes RFC1-Related Disorder from Other Late-Onset Ataxias
Camila C Lobo, Guilherme S O Wertheimer, Gabriel S Schmitt, et al.
Brain : a Journal of Neurology
|
October 19, 2021
Primary neural leprosy: clinical, neurophysiological and pathological presentation and progression
Pedro J Tomaselli, Diogo F Dos Santos, André C J Dos Santos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 12, 2018
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response
Ingrid Faber, Alberto Rolim Muro Martinez, Carlos Roberto Martins, et al.
Page
of 20