Results 11 to 20 of about 6,580 (114)

Qualidade de vida em pacientes com doença de Machado-Joseph sob acompanhamento fonoaudiológico para disfagia

open access: yesRevista CEFAC
RESUMO A doença de Machado-Joseph é uma doença degenerativa e atualmente considerada a ataxia espinocerebelar mais frequente. O processo degenerativo da doença afeta diferentes regiões e funções do sistema nervoso central e/ou periférico. A disfagia é um
Bibiana Fuzer da Silva   +2 more
doaj   +2 more sources

Curva de Crescimento Usando Modelo Misto: Uma Aplicação na Progressão da Doença de Machado-Joseph

open access: yesClinical and Biomedical Research, 2009
Introdução: a obtenção dos dados por meio de medidas repetidas em diversas ocasiões no tempo em um mesmo sujeito torna possível o ajuste de curvas que descrevam padrões de evolução e identificam preditores de evolução.
Lisiane Hauser   +5 more
doaj   +2 more sources

UEG Week 2022 Poster Presentations [PDF]

open access: yesUnited European Gastroenterol J, 2022
United European Gastroenterology Journal, Volume 10, Issue S8, Page 473-1092, October 2022.
europepmc   +2 more sources

Geographic patterns of tree dispersal modes in Amazonia and their ecological correlates

open access: yesGlobal Ecology and Biogeography, Volume 32, Issue 1, Page 49-69, January 2023., 2023
Abstract Aim To investigate the geographic patterns and ecological correlates in the geographic distribution of the most common tree dispersal modes in Amazonia (endozoochory, synzoochory, anemochory and hydrochory). We examined if the proportional abundance of these dispersal modes could be explained by the availability of dispersal agents (disperser ...
Diego F. Correa   +207 more
wiley   +1 more source

Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3

open access: yesMovement Disorders, Volume 37, Issue 9, Page 1850-1860, September 2022., 2022
Abstract Background Disease severity in spinocerebellar ataxia type 3 (SCA3) is commonly defined by the Scale for the Assessment and Rating of Ataxia (SARA) sum score, but little is known about the contributions and progression patterns of individual items.
Roderick P.P.W.M. Maas   +22 more
wiley   +1 more source

Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity

open access: yesMovement Disorders, Volume 37, Issue 2, Page 405-410, February 2022., 2022
ABSTRACT Background Lifestyle could influence the course of hereditary ataxias, but representative data are missing. Objective The objective of this study was to characterize lifestyle in spinocerebellar ataxia type 3 (SCA3) and investigate possible associations with disease parameters.
Holger Hengel   +24 more
wiley   +1 more source

Polyglutamine‐Expanded Ataxin‐3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood

open access: yesMovement Disorders, Volume 36, Issue 11, Page 2675-2681, November 2021., 2021
Abstract Background Spinocerebellar ataxia type 3 is a rare neurodegenerative disease caused by a CAG repeat expansion in the ataxin‐3 gene. Although no curative therapy is yet available, preclinical gene‐silencing approaches to reduce polyglutamine (polyQ) toxicity demonstrate promising results.
Jeannette Hübener‐Schmid   +23 more
wiley   +1 more source

UEG Week 2024 Poster Presentations [PDF]

open access: yesUnited European Gastroenterol J
United European Gastroenterology Journal, Volume 12, Issue S8, Page 665-1360, October 2024.
europepmc   +2 more sources

UEG Week 2014 Poster Presentations [PDF]

open access: yesUnited European Gastroenterol J, 2014
United European Gastroenterology Journal, Volume 2, Issue S1, Page A132-A605, October 2014.
europepmc   +2 more sources

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