Denes Zadori
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Explore the profile of Denes Zadori including associated specialties, affiliations and a list of published articles.
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93
Citations
796
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Recent Articles
1.
Szabo M, Gardian G, Szpisjak L, Salamon A, Gabor T, Klivenyi P, et al.
Mov Disord Clin Pract
. 2024 Jun;
11(8):1013-1017.
PMID: 38828630
Background: Due to its heterogeneous manifestation an individualized approach to reach therapeutic goals in cervical dystonia (CD) is advantageous. Objectives: The aim of the current study was to adapt goal...
2.
Szalardy L, Fakan B, Maszlag-Torok R, Ferencz E, Reisz Z, Radics B, et al.
Neuropathol Appl Neurobiol
. 2023 Dec;
50(1):e12946.
PMID: 38093468
Aims: Cerebral amyloid angiopathy (CAA)-related inflammation (CAA-RI) is a potentially reversible manifestation of CAA, histopathologically characterised by transmural and/or perivascular inflammatory infiltrates. We aimed to identify clinical, radiological and laboratory...
3.
Salamon A, Nagy Z, Pal M, Szabo M, Csosz A, Szpisjak L, et al.
Int J Mol Sci
. 2023 Jul;
24(13).
PMID: 37445923
Dystonia is a rare movement disorder which is characterized by sustained or intermittent muscle contractions causing abnormal and often repetitive movements, postures, or both. The two most common forms of...
4.
Szabo M, DO Kiem D, Gardian G, Szpisjak L, Salamon A, Klivenyi P, et al.
Ideggyogy Sz
. 2023 Mar;
76(1-2):37-45.
PMID: 36892297
Background And Purpose: Cervical dystonia (CD) is the most common form of focal dystonias, where the identification of the involved muscles, the determination of optimal botulinum neurotoxin A (BoNT-A) dose...
5.
Klivenyi P, Szpisjak L, Salamon A, Nemeth V, Szepfalusi N, Maroti Z, et al.
Ideggyogy Sz
. 2023 Mar;
76(1-2):63-72.
PMID: 36892293
Spinocerebellar ataxia type 48 (SCA48) is an autosomal dominantly inherited disease characterized by gait and limb ataxia, cerebellar dysarthria, cognitive impairment, psychiatric abnormalities and variable types of movement disorders. To...
6.
Boros F, Szpisjak L, Bozo R, Kelemen E, Zadori D, Salamon A, et al.
Int J Mol Sci
. 2023 Feb;
24(3).
PMID: 36768938
Spinocerebellar ataxia (SCA) 40 is an extremely rare subtype of the phenotypically and genetically diverse autosomal dominant ataxias caused by mutations of the gene. Most reported cases of SCA40 are...
7.
Salamon A, Zadori D, Szpisjak L, Klivenyi P, Vecsei L
Expert Opin Ther Targets
. 2022 Dec;
26(10):827-836.
PMID: 36524726
Introduction: Parkinson's disease (PD) is the second most common neurodegenerative disease worldwide. The median age of disease onset is around 60 years. From a genetic point of view, PD is...
8.
Kelemen A, Halasz L, Muthuraman M, Eross L, Barsi P, Zadori D, et al.
Front Neurol
. 2022 Oct;
13:917187.
PMID: 36226087
We investigated the effect of deep brain stimulation on dynamic balance during gait in Parkinson's disease with motion sensor measurements and predicted their values from disease-related factors. We recruited twenty...
9.
Vereb D, Kovacs M, Antal S, Kocsis K, Szabo N, Kincses B, et al.
Front Neurol
. 2022 Aug;
13:927481.
PMID: 36016543
Visual dysfunction is a recognized early symptom of Parkinson's disease (PD) that partly scales motor symptoms, yet its background is heterogeneous. With additional deficits in visuospatial attention, the two systems...
10.
Salamon A, Zadori D, Szpisjak L, Klivenyi P, Vecsei L
Expert Opin Pharmacother
. 2022 Apr;
23(10):1123-1128.
PMID: 35373688
No abstract available.