Juvenile Gerstmann-Straussler-Scheinker Disease Mimicking Anticipation Phenomenon (2023)
- Authors:
- Autor USP: ZANOTELI, EDMAR - FM
- Unidade: FM
- DOI: 10.1002/mdc3.13878
- Subjects: CEREBELO; ATAXIA
- Language: Inglês
- Imprenta:
- Source:
- Título: MOVEMENT DISORDERS CLINICAL PRACTICE
- ISSN: 2330-1619
- Volume/Número/Paginação/Ano: v. 10, n. 11, p. 1700-1702, 2023
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
-
ABNT
SILVA, Thiago Yoshinaga Tonholo et al. Juvenile Gerstmann-Straussler-Scheinker Disease Mimicking Anticipation Phenomenon. MOVEMENT DISORDERS CLINICAL PRACTICE, v. 10, n. 11, p. 1700-1702, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/57971. Acesso em: 08 jan. 2026. -
APA
Silva, T. Y. T., Marques, M. V. O., Zanoteli, E., Pedroso, J. L., & Barsottini, O. G. P. (2023). Juvenile Gerstmann-Straussler-Scheinker Disease Mimicking Anticipation Phenomenon. MOVEMENT DISORDERS CLINICAL PRACTICE, 10( 11), 1700-1702. doi:10.1002/mdc3.13878 -
NLM
Silva TYT, Marques MVO, Zanoteli E, Pedroso JL, Barsottini OGP. Juvenile Gerstmann-Straussler-Scheinker Disease Mimicking Anticipation Phenomenon [Internet]. MOVEMENT DISORDERS CLINICAL PRACTICE. 2023 ; 10( 11): 1700-1702.[citado 2026 jan. 08 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57971 -
Vancouver
Silva TYT, Marques MVO, Zanoteli E, Pedroso JL, Barsottini OGP. Juvenile Gerstmann-Straussler-Scheinker Disease Mimicking Anticipation Phenomenon [Internet]. MOVEMENT DISORDERS CLINICAL PRACTICE. 2023 ; 10( 11): 1700-1702.[citado 2026 jan. 08 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57971 - Myopathy due to HMGCR antibodies in adult mimicking muscular dystrophy associated with cancer and statin exposure - narrative review of the literature - case report
- Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies
- Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study
- Whole-Body MRI in Limb Girdle Muscular Dystrophy Type R1/2A: Correlation With Clinical Scores
- Rhabdomyolysis: a genetic perspective
- A new mutation in PYGM causing McArdle disease in a Brazilian patient [Carta]
- STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility
- Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues
- Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series
- Therapeutic advances in 5q-linked spinal muscular atrophy
Informações sobre o DOI: 10.1002/mdc3.13878 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
