Detalhe da pesquisa
1.
Optimizing the electronic medical record to improve patient care and conduct quality improvement initiatives in a concussion specialty clinic.
Brain Inj
; 34(1): 62-67, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31644325
2.
Structured Clinical Documentation to Improve Quality and Support Practice-Based Research in Headache.
Headache
; 58(8): 1211-1218, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30066412
3.
Mortality risk factors in newly diagnosed diabetic cardiac autonomic neuropathy.
Clin Auton Res
; 33(6): 903-907, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37695385
4.
Investigating ioflupane I123 injection and single photon emission tomography as an imaging biomarker for long-term sequelae following mild traumatic brain injury.
Brain Inj
; 32(1): 105-112, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29131690
5.
Structured clinical documentation in the electronic medical record to improve quality and to support practice-based research in epilepsy.
Epilepsia
; 58(1): 68-76, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27864833
6.
MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies.
Alzheimers Dement
; 12(12): 1297-1304, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287057
7.
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS Genet
; 8(3): e1002548, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22438815
8.
A road map for efficient and reliable human genome epidemiology.
Nat Genet
; 38(1): 3-5, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16468121
9.
Translation initiator EIF4G1 mutations in familial Parkinson disease.
Am J Hum Genet
; 89(3): 398-406, 2011 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21907011
10.
Alpha-synuclein repeat variants and survival in Parkinson's disease.
Mov Disord
; 29(8): 1053-7, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24578302
11.
Mutations in CIZ1 cause adult onset primary cervical dystonia.
Ann Neurol
; 71(4): 458-69, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22447717
12.
Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.
Mov Disord
; 28(12): 1740-4, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23913756
13.
Evaluation of a Computable Phenotype for Successful Cognitive Aging.
Mayo Clin Proc Innov Qual Outcomes
; 7(4): 212-221, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37304063
14.
A blood biomarker test for brain amyloid impacts the clinical evaluation of cognitive impairment.
Ann Clin Transl Neurol
; 10(10): 1738-1748, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37550958
15.
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
Ann Neurol
; 69(5): 778-92, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21391235
16.
Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease.
PLoS Genet
; 10(11): e1004788, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25412286
17.
Mediterranean diet adherence, gut microbiota, and Alzheimer's or Parkinson's disease risk: A systematic review.
J Neurol Sci
; 434: 120166, 2022 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35144237
18.
Axon guidance and synaptic maintenance: preclinical markers for neurodegenerative disease and therapeutics.
Trends Neurosci
; 32(3): 142-9, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19162339
19.
Variants in estrogen-related genes and risk of Parkinson's disease.
Mov Disord
; 26(7): 1234-42, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21469201
20.
Common variants in PARK loci and related genes and Parkinson's disease.
Mov Disord
; 26(2): 280-8, 2011 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21412835