Detalhe da pesquisa
1.
Identifying diagnostic and prognostic factors in cerebral amyloid angiopathy-related inflammation: A systematic analysis of published and seven new cases.
Neuropathol Appl Neurobiol
; 50(1): e12946, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38093468
2.
Genetic Screening of a Hungarian Cohort with Focal Dystonia Identified Several Novel Putative Pathogenic Gene Variants.
Int J Mol Sci
; 24(13)2023 Jun 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37445923
3.
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene.
Int J Mol Sci
; 24(3)2023 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36768938
4.
Clinical features of cervical dystonia patients classified by the COL-CAP concept and treated with ultrasound-guided botulinum neurotoxin.
Ideggyogy Sz
; 76(1-2): 37-45, 2023 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36892297
5.
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient].
Ideggyogy Sz
; 76(1-2): 63-72, 2023 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36892293
6.
Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study.
BMC Neurosci
; 22(1): 7, 2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33526008
7.
Hereditary and non-hereditary etiologies associated with extensive brain calcification: case series.
Metab Brain Dis
; 36(7): 2131-2139, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34287746
8.
Atypical presentation of late-onset Sandhoff disease: a case report.
Ideggyogy Sz
; 74(11-12): 425-429, 2021 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34856081
9.
Multiphasic presentation of neuralgic amyotrophy associated with hepatitis E virus infection.
Muscle Nerve
; 61(1): 108-110, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31573093
10.
Neuroprotection in Parkinson's disease: facts and hopes.
J Neural Transm (Vienna)
; 127(5): 821-829, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31828513
11.
Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene-case series.
Neurol Sci
; 41(1): 125-129, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31478152
12.
Novel AARS2 gene mutation producing leukodystrophy: a case report.
J Hum Genet
; 62(2): 329-333, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27734837
13.
Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series.
Neurol Sci
; 38(3): 481-483, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27888347
14.
The establishment of tocopherol reference intervals for Hungarian adult population using a validated HPLC method.
Biomed Chromatogr
; 31(9)2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28182842
15.
Correction to: Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study.
BMC Neurosci
; 22(1): 16, 2021 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33691616
16.
The Application of Goal Attainment Scaling in Cervical Dystonia - An Exploratory Observational Pilot Study.
Mov Disord Clin Pract
; 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38828630
17.
Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation.
Cerebellum
; 16(5-6): 979-985, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28660440
18.
The genetic background of Parkinson's disease and novel therapeutic targets.
Expert Opin Ther Targets
; 26(10): 827-836, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36524726
19.
Fixed-dose combination therapy for Parkinson's disease with a spotlight on entacapone in the past 20 years: a reduced pill burden and a simplified dosing regime.
Expert Opin Pharmacother
; 21(18): 2265-2278, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32808807
20.
Connection between small vessel disease related stroke and the MTHFR C677T polymorphism in a Hungarian population.
Heliyon
; 6(11): e05305, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33163671