Detalhe da pesquisa
1.
Single Residue Variation in Skeletal Muscle Myosin Enables Direct and Selective Drug Targeting for Spasticity and Muscle Stiffness.
Cell
; 183(2): 335-346.e13, 2020 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33035452
2.
Urinary titin in myotonic dystrophy type 1.
Muscle Nerve
; 68(2): 215-218, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37291994
3.
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study.
J Neurol Neurosurg Psychiatry
; 2022 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35896379
4.
Investigation of oxidative stress in patients with multifocal motor neuropathy.
Ideggyogy Sz
; 75(11-12): 385-393, 2022 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36541147
5.
The role of hybrid FDG-PET/MRI on decision-making in presurgical evaluation of drug-resistant epilepsy.
BMC Neurol
; 21(1): 363, 2021 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34537017
6.
Protective Effects of PACAP in a Rat Model of Diabetic Neuropathy.
Int J Mol Sci
; 22(19)2021 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34639032
7.
[Diseases with peripheral motor symptoms]. / Perifériás motoros tünettannal társuló kórképek.
Ideggyogy Sz
; 73(3-4): 85-98, 2020 Mar 30.
Artigo
em Húngaro
| MEDLINE | ID: mdl-32364336
8.
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
BMC Med Genet
; 18(1): 105, 2017 09 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28927399
9.
Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
BMC Med Genet
; 18(1): 150, 2017 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29248012
10.
Elevated FGF 21 in myotonic dystrophy type 1 and mitochondrial diseases.
Muscle Nerve
; 55(4): 564-569, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27489983
11.
[Rhabdomyolysis - may it be a metabolic myopathy? Case report and diagnostic algorithm]. / Rhabdomyolysis Mikor vessük fel metabolikus myopathia lehetoségét? Esetismertetés és diagnosztikus algoritmus.
Orv Hetil
; 158(47): 1873-1882, 2017 Nov.
Artigo
em Húngaro
| MEDLINE | ID: mdl-29153022
12.
High-Frequency Repetitive Transcranial Magnetic Stimulation Can Improve Depression in Parkinson's Disease: A Randomized, Double-Blind, Placebo-Controlled Study.
Neuropsychobiology
; 73(3): 169-77, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27093063
13.
The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy.
Clin Neuropathol
; 34(2): 89-95, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25492887
14.
[VALIDATION OF THE HUNGARIAN UNIFIED DYSKINESIA RATING SCALE]. / AZ EGYSÉGESÍTETT DYSKINESIA-PONTOZÓSKÁLA MAGYAR NYELVI VALIDÁCIÓJA.
Ideggyogy Sz
; 68(5-6): 183-8, 2015 May 30.
Artigo
em Húngaro
| MEDLINE | ID: mdl-26182609
15.
[VALIDATION OF THE HUNGARIAN MDS-UPDRS: WHY DO WE NEED A NEW PARKINSON SCALE?]. / AZ MDS-UPDRS MAGYAR VALIDáCIóJA: MIéRT SZüKSéGES UJABB PARKINSON-PONTOZOSKáLA?
Ideggyogy Sz
; 67(3-4): 129-34, 2014 Mar 30.
Artigo
em Húngaro
| MEDLINE | ID: mdl-26118257
16.
Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey.
J Neuromuscul Dis
; 10(2): 173-184, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36373291
17.
Clinical Classification of Variants in the Valosin-Containing Protein Gene Associated With Multisystem Proteinopathy.
Neurol Genet
; 9(5): e200093, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37588275
18.
Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis.
J Neurol
; 270(12): 5849-5865, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37603075
19.
[Diagnosis and therapy of mitochondrial diseases]. / Mitochondrialis betegségek diagnosztikája es terápiája.
Ideggyogy Sz
; 65(7-8): 229-37, 2012 Jul 30.
Artigo
em Húngaro
| MEDLINE | ID: mdl-23074842
20.
[Risk factors for ischaemic stroke in myotonic dystrophy type 1]. / Az ischaemiás stroke kockázati tényezoi a dystrophia myotonica 1-es típusában.
Orv Hetil
; 163(49): 1962-1966, 2022 Dec 04.
Artigo
em Húngaro
| MEDLINE | ID: mdl-36463553