Results 31 to 40 of about 2,400 (108)

Effect of an intervention protocol based on motor learning for walking and balance in young patient with primary lateral sclerosis: a case study [PDF]

, 2021
Introduction: Primary lateral sclerosis (PLS) is a rare disease characterized by the upper motor neuron degeneration that usually begin in the sixth decade of life. It has an insidious onset of symmetrical, slowly progressive spastic paresis, which often
Castellanos Ruiz, Julialba, García García, Clara Inés, Pinzón Bernal, Mónica Yamile, Silva Filho, João Antonio da   +3 more
core   +2 more sources

Amyotrophic lateral sclerosis with dementia: case report Esclerose lateral amiotrófica com demência: relato de caso

Arquivos de Neuro-Psiquiatria, 1999
A patient is described in whom a profound and rapidly progressive dementia occurred in association with clinical features of amyotrophic lateral sclerosis. A magnetic resonance imaging showed signs of frontal and especially left temporal atrophy.
PAULO ROBERTO DE BRITO-MARQUES, ROBERTO VIEIRA DE MELLO   +1 more
doaj   +1 more source

Transcriptomic profiling of dorsal root ganglia in atopic and healthy dogs: A comparative RNA sequencing study with implications in cutaneous itch research

Veterinary Dermatology, Volume 36, Issue 4, Page 401-411, August 2025.
Background – Itch is a common symptom in skin disorders. While the neural pathways of itch transmission from the skin to the brain are well‐understood in rodents, the same pathways in dogs remain unclear. The knowledge gap hinders the development of effective treatments for canine itch‐related disorders.
Chie Tamamoto‐Mochizuki, Santosh K. Mishra   +1 more
wiley   +1 more source

Poliomielite. [PDF]

, 1987
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Nogueira, Antônio Fernando Nastri
core   +3 more sources

Ortopneia não cardiogénica. A propósito de dois casos de esclerose lateral amiotrófica

Revista Portuguesa de Pneumologia, 1997
RESUMO: A literatura regista muito poucos casos de doença do neurónio motor que apresentem como manifestação inaugural dispneia por paralisia do diafragma.Por outro lado, o diagnóstico de paralisia do diafragma como causa de falência respiratória é, em ...
Pilar Azevedo, J. Valença, G. Brum, F. Caeiro, F. Monteiro, J. Rosal Gonçalves, J.T. Monteiro, A. Couto, M. Freitas e Costa   +8 more
doaj   +1 more source

X-linked spinal and bulbar muscular atrophy (Kennedy's disease) with long-term electrophysiological evaluation: case report Atrofia muscular bulbo-espinal ligada ao cromossomo X (doença de Kennedy) com seguimento eletrofisiológico de longo prazo: relato de caso

Arquivos de Neuro-Psiquiatria, 2005
X-linked spinal and bulbar muscular atrophy or Kennedy's disease is an adult-onset motor neuronopathy caused by a CAG repeat expansion within the first exon of an androgen receptor gene.
João Aris Kouyoumdjian, Maria da Penha Ananias Morita, Rogério Gayer Machado de Araújo   +2 more
doaj   +1 more source

Evidences for guiding of the physical therapeutic intervention in the kinetic-functional alterations generated by the amyotrophic lateral sclerosis [PDF]

, 2012
Os questionamentos sobre a recomendação ou não de exercícios regulares e outros recursos fisioterapêuticos para pacientes portadores de esclerose lateral amiotrófica ainda geram discussões controversas.
Honorato, Elizabeth Silva, Martins, Emerson Fachin   +1 more
core  

Porfiria aguda intermitente: valor do teste de Watson e Schwartz para o diagnóstico

Arquivos de Neuro-Psiquiatria, 1957
É apresentado um caso de Porfiria aguda intermitente em uma jovem de 20 anos do sexo feminino. Os primeiros sintomas - cólicas abdominais periódicas - surgiram aos 15 anos de idade.
José Lamartine de Assis
doaj   +1 more source

The review of the methods to obtain non-neuronal cells to study glial influence on Amyotrophic Lateral Sclerosis pathophysiology at molecular level in vitro Revisão dos métodos de obtenção de células não neuronais para o estudo da fisiopatologia da Esclerose Lateral Amiotrófica ao nível molecular in vitro

Acta Cirúrgica Brasileira, 2010
PURPOSE: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that displays a rapid evolution. Current treatments have failed to revert clinical symptoms because the mechanisms involved in the death of motoneuron are still unknown ...
Juliana Milani Scorisa, Tatiana Duobles, Gabriela Pintar de Oliveira, Jessica Ruivo Maximino, Gerson Chadi   +4 more
doaj   +1 more source

Clinical and molecular analysis of spinal muscular atrophy in Brazilian patients

Genetics and Molecular Biology, 1999
Spinal muscular atrophy (SMA), the second most common lethal autosomal recessive disorder, has an incidence of 1:10,000 newborns. SMA is divided into acute (Werdnig-Hoffmann disease, type I), intermediate (type II) and juvenile forms (Kugelberg-Welander ...
C.A. Kim, M.R. Passos-Bueno, S.K. Marie, A. Cerqueira, U. Conti, M.J. Marques-Dias, C.H. Gonzalez, M. Zatz   +7 more
doaj   +1 more source