Detalhe da pesquisa
1.
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insights.
J Med Genet
; 61(5): 443-451, 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38458754
2.
Cultural adaptation and clinical validation of Rapid Cognitive Screening Test in Turkish.
Psychogeriatrics
; 24(1): 87-93, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37990418
3.
An Investigation of Affective Personality Traits in Alzheimer's Disease: SEEKING as a Possible Predictor for Early-Stage Alzheimer's Dementia.
Exp Aging Res
; : 1-14, 2023 Sep 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37695698
4.
A comprehensive analysis of copy number variation in a Turkish dementia cohort.
Hum Genomics
; 15(1): 48, 2021 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34321086
5.
Anticholinergic Burden, Polypharmacy, and Cognition in Parkinson's Disease Patients with Mild Cognitive Impairment: A Cross-Sectional Observational Study.
Dement Geriatr Cogn Disord
; 51(5): 386-395, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36273437
6.
Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review.
BMC Neurol
; 22(1): 122, 2022 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35346091
7.
Does transcranial direct current stimulation enhance cognitive performance in Parkinson's disease mild cognitive impairment? An event-related potentials and neuropsychological assessment study.
Neurol Sci
; 43(6): 4029-4044, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35322340
8.
Identification of metabolic correlates of mild cognitive impairment in Parkinson's disease using magnetic resonance spectroscopic imaging and machine learning.
MAGMA
; 35(6): 997-1008, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35867235
9.
Genetic variants of vitamin D metabolism-related DHCR7/NADSYN1 locus and CYP2R1 gene are associated with clinical features of Parkinson's disease.
Int J Neurosci
; 132(5): 439-449, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32938288
10.
Characterization of Recessive Parkinson Disease in a Large Multicenter Study.
Ann Neurol
; 88(4): 843-850, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33045815
11.
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
Mov Disord
; 36(7): 1676-1688, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33624863
12.
TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features.
Eur J Neurol
; 28(8): 2603-2613, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33969597
13.
A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Neurol Sci
; 42(7): 2969-2973, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33559790
14.
A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's disease.
Neurol Sci
; 42(6): 2497-2504, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33855622
15.
A novel PNPLA6 mutation in a Turkish family with intractable Holmes tremor and spastic ataxia.
Neurol Sci
; 42(4): 1535-1539, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33210227
16.
Neurological features and outcomes of Wilson's disease: a single-center experience.
Neurol Sci
; 42(9): 3829-3834, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33474589
17.
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database.
Hum Mutat
; 41(8): e7-e45, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32579787
18.
The cerebral blood flow deficits in Parkinson's disease with mild cognitive impairment using arterial spin labeling MRI.
J Neural Transm (Vienna)
; 127(9): 1285-1294, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32632889
19.
Do Alzheimer's Disease Patients Appear Younger than Their Real Age?
Dement Geriatr Cogn Disord
; 49(5): 483-488, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33080614
20.
Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease's patients.
Mol Biol Rep
; 47(8): 5903-5909, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32681391