Buscar
Mostrando ítems 1-10 de 556
The frequency of the C9orf72 expansion in a Brazilian population
(Elsevier, 2023)
Prevalence of C9orf72 hexanucleotide repeat expansion in Greek patients with sporadic ALS
(Taylor & Francis, 2020-07)
A total of 178 consecutive patients with definite sALS without frontotemporal dementia (FTD) were enrolled in this study, after complete clinical evaluation. A Repeat-Primed Polymerase Chain Reaction (RP-PCR) protocol was ...
Electrophysiological evaluation in myotonic dystrophy - Correlation with CTG length expansion
(Assoc Arquivos De Neuro- PsiquiatriaSao Paulo SpBrasil, 2001)
Analysis of the DMPK gene CTG repeat in healthy Brazilians
(Sociedade Brasileira de Genética, 2019)
Number of repeating digits in base b expansion of fractions
(Wolfram demonstrations project, 2016)
Number of repeating digits in base b expansion of fractions
(Wolfram demonstrations project, 2013)
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.
(Springer, 2015-05)
The most common cause of both amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) is a G4C2-repeat expansion in C9orf72. However, the lower limit for pathological repeats has not been established ...
Analysis of C9orf72 in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Argentina
(Elsevier Science Inc, 2016-04)
Pathologic expansion of the G4C2 repeat in C9orf72 is the main genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). To evaluate the frequency of the G4C2 expansion in a Latin American ...