Zobrazeno 1 - 10
of 556
pro vyhledávání: '"Hélio A.G Teive"'
Autor:
Gustavo L. Franklin, Hélio A.G. Teive
Publikováno v:
Brazilian Journal of Psychiatry, Vol 43, Iss 2, Pp 222-222 (2020)
Externí odkaz:
https://doaj.org/article/47aa9ffddfc34b619e70f9c4dfa73edc
Autor:
Francisco M.B. Germiniani, Olivier Walusinski, Matheus Kahakura Franco Pedro, Hélio A.G. Teive, Thiago Ferreira de Souza
Publikováno v:
Arquivos de Neuro-Psiquiatria, Issue: ahead, Published: 01 OCT 2021
Arquivos de Neuro-Psiquiatria, Volume: 79, Issue: 12, Pages: 1145-1148, Published: 01 OCT 2021
Arquivos de Neuro-Psiquiatria v.79 n.12 2021
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria
Arquivos de Neuro-Psiquiatria, Volume: 79, Issue: 12, Pages: 1145-1148, Published: 01 OCT 2021
Arquivos de Neuro-Psiquiatria v.79 n.12 2021
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria
André Brouillet’s (1857-1914) famous group tableau ‘A Clinical Lesson at La Salpêtrière’ (French: Une leçon clinique à la Salpêtrière) is possibly the most celebrated painting in the history of neurology. His depiction of one of Jean-Mar
Autor:
José Luiz Pedroso, Marcelo Andrés Kauffman, Renato P. Munhoz, Hélio A.G. Teive, Thiago Cardoso Vale, Orlando Graziani Povoas Barsottini, Marcondes Cavalcante França Junior
Publikováno v:
The Cerebellum. 21:1073-1084
Spastic ataxia is characterized by the combination of cerebellar ataxia with spasticity and other pyramidal features. It is the hallmark of some hereditary ataxias, but it can also occur in some spastic paraplegias and acquired conditions. It often p
Autor:
Carlos Henrique Ferreira Camargo, Nicolás Sommaruga, Olivier Walusinski, Hélio A.G. Teive, Héctor Ignacio Amorin-Costábile
Publikováno v:
Journal of Clinical Neuroscience. 91:172-175
Introduction The Uruguayan physician Francisco Soca, who specialized in neurology in Jean-Martin Charcot’s clinic, defended a thesis at the Paris Faculty of Medicine in 1888 on Friedreich's ataxia in eleven patients. In this work he described the p
Autor:
Adriana Moro, Renato P. Munhoz, Walter O. Arruda, Salmo Raskin, Mariana Moscovich, Hélio A.G. Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 9, Pp 659-662 (2014)
Spinocerebellar ataxia type 3 (SCA3) involves cerebellar, pyramidal, extrapyramidal, motor neuron and oculomotor systems with strong phenotypic heterogeneity, that lead us to classify the disorder into different clinical subtypes according to the pre
Externí odkaz:
https://doaj.org/article/14fce1d8b73d4321b216e62f57484cd6
Autor:
Carlos Henrique Ferreira Camargo, Hélio A.G. Teive, Marina Siqueira Campos Bastos, Renato Nickel
Publikováno v:
Mov Disord Clin Pract
BACKGROUND: Cervical dystonia (CD) involves clinical and motor manifestations, and visual and cognitive dysfunctions may also be frequent. OBJECTIVE: To evaluate functional vision, visual attention, and cognitive aspects in patients with CD compared
Autor:
João Carlos Papaterra Limongi, Olivier Walusinski, Carlos Henrique Ferreira Camargo, Hélio A.G. Teive, Egberto Reis Barbosa, Paulina Cunha, Yves Agid, Matheus Gomes Ferreira
Publikováno v:
Neurological Sciences. 42:5413-5417
Raymond Garcin, professor of neurology in Paris, France, and his Brazilian assistant, Professor Roberto Melaragno described in 1948 the phenomenon defined as "begaiement de la mise en route du mouvement" in patients with Parkinson's disease. This was
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 8, Pp 743-747 (2021)
Over the past 68 years, the Finkel type late-onset adult autosomal dominant spinal muscular atrophy (SMA) that is allelic with amyotrophic lateral sclerosis-8 (ALS8) gained a genotype-phenotype correlation among the motor neuron diseases through the
Publikováno v:
Brain. 144:3547-3549
Language and its associated disorders have puzzled humanity since the dawn of civilization. The first descriptions of aphasia go back to classical antiquity. The Egyptians and Babylonians believed speech was a divine gift to mortals, and their descri
Autor:
S Catherine Díaz, Matheus Gomes Ferreira, Marcelo Miranda, María Leonor Bustamante, J Valentina Castillo, Hélio A.G. Teive
Publikováno v:
The Cerebellum. 20:938-941
Autosomal recessive cerebellar ataxia type 1 (ARCA-1) or spinocerebellar ataxia autosomal recessive type 8 (SCAR8) is a slowly progressive neurodegenerative disorder that occurs due to mutations in the spectrin repeat containing nuclear envelope prot