Atypical clinical course of FXTAS: rapidly progressive dementia as the major symptom (2007)
- Authors:
- USP affiliated authors: NITRINI, RICARDO - FM ; MORGANTE, ANGELA MARIA VIANNA - IB
- Schools: FM; IB
- Subjects: DOENÇAS NEURODEGENERATIVAS; DEMÊNCIA
- Language: Inglês
- Imprenta:
- Place of publication: Philadelphia
- Date published: 2007
- Source:
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ABNT
GONÇALVES, M. R. R; CAPELLI, Leonardo Pires; NITRINI, Ricardo; et al. Atypical clinical course of FXTAS: rapidly progressive dementia as the major symptom. Neurology, Philadelphia, v. 68, n. 21, p. 1864-1866, 2007. -
APA
Gonçalves, M. R. R., Capelli, L. P., Nitrini, R., Barbosa, E. R., Porto, C. S., Lucato, L. T., & Vianna-Morgante, A. M. (2007). Atypical clinical course of FXTAS: rapidly progressive dementia as the major symptom. Neurology, 68( 21), 1864-1866. -
NLM
Gonçalves MRR, Capelli LP, Nitrini R, Barbosa ER, Porto CS, Lucato LT, Vianna-Morgante AM. Atypical clinical course of FXTAS: rapidly progressive dementia as the major symptom. Neurology. 2007 ; 68( 21): 1864-1866. -
Vancouver
Gonçalves MRR, Capelli LP, Nitrini R, Barbosa ER, Porto CS, Lucato LT, Vianna-Morgante AM. Atypical clinical course of FXTAS: rapidly progressive dementia as the major symptom. Neurology. 2007 ; 68( 21): 1864-1866. - Clinical and genetic studies in the fragile X-associated tremor ataxia syndrome (FXTAS), caused by FMR1 gene premutations
- Fragile X-associated tremor/ataxia syndrome: intrafamilial variability and the size of the FMR1 premutation CGG repeat
- The fragile x-associated tremor and ataxia syndrome (FXTAS)
- Sindrome fg associada com a mutacao da sindrome do cromossomo x fragil
- Simple, rapid and inexpensive quantitative fluorescent PCR method for detection of microdeletion and microduplication syndromes
- Mapeamento dos pontos de quebra em uma translocação t(2;22) familial associada a alterações fenotípicas
- Um cromossomo marcador extranumerário sem seqüência alfóide: análise por microdissecção e fish
- FMR1 and premature ovarian failure
- Altered subcellular distribution of fragile X mental retardation protein (FMRP) in BDNF- treated neurons showing dysmorphic dendritic spines
- Sequencing of the breakpoint junction fragments of an X; autosome translocation in a female with Duchenne muscular dystrophy
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