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Neuroprotection in Parkinson’s disease: facts and hopes

Journal of Neural Transmission, 2020-05, Vol.127 (5), p.821-829

2020

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Genetic Screening of a Hungarian Cohort with Focal Dystonia Identified Several Novel Putative Pathogenic Gene Variants

International journal of molecular sciences, 2023-06, Vol.24 (13), p.10745

2023

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Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene

International journal of molecular sciences, 2023-01, Vol.24 (3), p.2617

2023

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Hereditary and non-hereditary etiologies associated with extensive brain calcification: case series

Metabolic brain disease, 2021-10, Vol.36 (7), p.2131-2139

2021

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Clinical features of cervical dystonia patients classified by the COL-CAP concept and treated with ultrasound-guided botulinum neurotoxin

Ideggyógyászati szemle, 2023-01, Vol.76 (1-2), p.37

2023

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Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient

Ideggyógyászati szemle, 2023-01, Vol.76 (1-2), p.63

2023

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Connection between small vessel disease related stroke and the MTHFR C677T polymorphism in a Hungarian population

Heliyon, 2020-11, Vol.6 (11), p.e05305-e05305, Article e05305

2020

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Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene—case series

Neurological sciences, 2020-01, Vol.41 (1), p.125-129

2020

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Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series

Neurological sciences, 2017-03, Vol.38 (3), p.481-483

2017

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The establishment of tocopherol reference intervals for Hungarian adult population using a validated HPLC method

Biomedical chromatography, 2017-09, Vol.31 (9), p.n/a

2017

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What is the impact of catechol-O-methyltransferase (COMT) on Parkinson's disease treatment?

Expert opinion on pharmacotherapy, 2022-07, Vol.23 (10), p.1123-1128

2022

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Atypical presentation of late-onset Sandhoff disease: a case report

Ideggyógyászati szemle, 2021-11, Vol.74 (11-12), p.425

2021

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Multiphasic presentation of neuralgic amyotrophy associated with hepatitis E virus infection

Muscle & nerve, 2020-01, Vol.61 (1), p.108-110

2020

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Opicapone for the treatment of Parkinson's disease: an update

Expert opinion on pharmacotherapy, 2019-12, Vol.20 (18), p.2201-2207

2019

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The genetic background of Parkinson's disease and novel therapeutic targets

Expert opinion on therapeutic targets, 2022-10, Vol.26 (10), p.827-836

2022

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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 opinion on pharmacotherapy, 2020-12, Vol.21 (18), p.2265-2278

2020

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Novel AARS2 gene mutation producing leukodystrophy: a case report

Journal of human genetics, 2017-02, Vol.62 (2), p.329-333

2017

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Novel AARS2 gene mutation producing leukodystrophy: a case report

Journal of human genetics, 2017-02, Vol.62 (2), p.329-333

2017

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Clinical and Genetic Characterization of Hereditary Ataxias

Szpisjak, László

2021

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ProQuest

Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study

BMC neuroscience, 2021-02, Vol.22 (1), p.7-7, Article 7

2021

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Correction to: Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study

BMC neuroscience, 2021-03, Vol.22 (1), p.16-16, Article 16

2021

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Comparison of the Outcome of Deep Brain Stimulator Surgeries in Parkinson’s Disease by Using Frame Based and Frameless Stereotactic Systems

Brain & spine, 2023, Vol.3, p.102287, Article 102287

2023

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The Application of Goal Attainment Scaling in Cervical Dystonia - An Exploratory Observational Pilot Study

Movement disorders clinical practice (Hoboken, N.J.), 2024-06

2024

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Successful multidisciplinary management of tetraplegia with a thoracic operation. Unicentric, mediastinal Castleman disease

Orvosi hetilap, 2020-01, Vol.161 (1), p.33

2020

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Selecting dopamine depleters for hyperkinetic movement disorders: how do we choose?

Expert opinion on pharmacotherapy, 2020-01, Vol.21 (1), p.1-4

2020

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Neuroprotection in Parkinson’s disease: facts and hopes

Genetic Screening of a Hungarian Cohort with Focal Dystonia Identified Several Novel Putative Pathogenic Gene Variants

Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene

Hereditary and non-hereditary etiologies associated with extensive brain calcification: case series

Clinical features of cervical dystonia patients classified by the COL-CAP concept and treated with ultrasound-guided botulinum neurotoxin

Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient

Connection between small vessel disease related stroke and the MTHFR C677T polymorphism in a Hungarian population

Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene—case series

Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series

The establishment of tocopherol reference intervals for Hungarian adult population using a validated HPLC method

What is the impact of catechol-O-methyltransferase (COMT) on Parkinson's disease treatment?

Atypical presentation of late-onset Sandhoff disease: a case report

Multiphasic presentation of neuralgic amyotrophy associated with hepatitis E virus infection

Opicapone for the treatment of Parkinson's disease: an update

The genetic background of Parkinson's disease and novel therapeutic targets

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

Novel AARS2 gene mutation producing leukodystrophy: a case report

Novel AARS2 gene mutation producing leukodystrophy: a case report

Clinical and Genetic Characterization of Hereditary Ataxias

Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study

Correction to: Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study

Comparison of the Outcome of Deep Brain Stimulator Surgeries in Parkinson’s Disease by Using Frame Based and Frameless Stereotactic Systems

The Application of Goal Attainment Scaling in Cervical Dystonia - An Exploratory Observational Pilot Study

Successful multidisciplinary management of tetraplegia with a thoracic operation. Unicentric, mediastinal Castleman disease

Selecting dopamine depleters for hyperkinetic movement disorders: how do we choose?

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