Detalhe da pesquisa
1.
Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients.
Acta Neuropathol
; 147(1): 28, 2024 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38305941
2.
The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15.
Brain
; 146(5): 2003-2015, 2023 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36315648
3.
Glucocerebrosidase reduces the spread of protein aggregation in a Drosophila melanogaster model of neurodegeneration by regulating proteins trafficked by extracellular vesicles.
PLoS Genet
; 17(2): e1008859, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33539341
4.
Complete home smoking ban survey analysis: an opportunity to improve health equity among sexual minority adults in California, USA.
BMC Public Health
; 22(1): 537, 2022 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35303831
5.
Embedding Equity in a Local Government's Response to COVID-19.
J Public Health Manag Pract
; 28(Suppl 1): S54-S57, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34797261
6.
Glucocerebrosidase deficiency promotes protein aggregation through dysregulation of extracellular vesicles.
PLoS Genet
; 14(9): e1007694, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30256786
7.
Randomised controlled trial of real-time feedback and brief coaching to reduce indoor smoking.
Tob Control
; 29(2): 183-190, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30770436
8.
Self-management of heart failure in dementia and cognitive impairment: a systematic review.
BMC Cardiovasc Disord
; 19(1): 99, 2019 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31035921
9.
Glucocerebrosidase Deficiency in Drosophila Results in α-Synuclein-Independent Protein Aggregation and Neurodegeneration.
PLoS Genet
; 12(3): e1005944, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27019408
10.
Unusually long duration and delayed penetrance in a family with FTD and mutation in MAPT (V337M).
Am J Med Genet B Neuropsychiatr Genet
; 174(1): 70-74, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26990251
11.
The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot.
Am J Med Genet B Neuropsychiatr Genet
; 171(7): 925-30, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27111571
12.
Vreteno, a gonad-specific protein, is essential for germline development and primary piRNA biogenesis in Drosophila.
Development
; 138(18): 4039-50, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21831924
13.
Complete home smoking bans and antitobacco contingencies: a natural experiment.
Nicotine Tob Res
; 16(2): 186-96, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23999652
14.
Enhancing Future Health Equity Plans: Insights from an Evaluation of Public Health Equity Resources in Oregon.
Health Equity
; 8(1): 26-31, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38250301
15.
Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias.
Mov Disord Clin Pract
; 11(5): 496-503, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38419568
16.
Two novel mutations in ABHD12: expansion of the mutation spectrum in PHARC and assessment of their functional effects.
Hum Mutat
; 34(12): 1672-8, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24027063
17.
Work-related musculoskeletal injury and suicide: opportunities for intervention and therapeutic jurisprudence.
J Law Med
; 21(1): 110-21, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24218786
18.
Recognizing junior doctors' potential contribution to patient safety and health care quality improvement.
J Health Organ Manag
; 27(2): 273-86, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23802403
19.
A pilot evaluation of an 8-week mindfulness-based stress reduction program for people with pre-symptomatic Huntington's disease.
J Community Genet
; 14(4): 395-405, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37458974
20.
Neurophysiological correlates of non-motor symptoms in late premanifest and early-stage manifest huntington's disease.
Clin Neurophysiol
; 153: 166-176, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37506604