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Guillain‐Barré syndrome during SARS‐CoV‐2 pandemic: A case report and review of recent literature

Journal of the peripheral nervous system, 2020-06, Vol.25 (2), p.204-207

2020

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Ultrasonography of MADSAM neuropathy: Focal nerve enlargements at sites of existing and resolved conduction blocks

Neuromuscular disorders : NMD, 2012-07, Vol.22 (7), p.627-631

2012

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The role of SCARB2 as susceptibility factor in Parkinson's disease

Movement disorders, 2013-04, Vol.28 (4), p.538-540

2013

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Psychiatric symptoms of patients with primary mitochondrial DNA disorders

Behavioral and brain functions, 2012-02, Vol.8 (1), p.9-9, Article 9

2012

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The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson’s Disease in the Hungarian Population

Parkinson's disease, 2018, Vol.2018 (2018), p.1-7

2018

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A susceptibility locus for Parkinson's disease maps to chromosome 2p13

Nature genetics, 1998-03, Vol.18 (3), p.262-265

1998

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Rare variants in PLXNA4 and Parkinson's disease

PloS one, 2013-11, Vol.8 (11), p.e79145-e79145

2013

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Guillain‐Barr é syndrome during SARS‐CoV ‐2 pandemic: A case report and review of recent literature

Journal of the peripheral nervous system, 2020-06, Vol.25 (2), p.204-207

2020

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P228 Reversible axonal conduction blocks and sonographic distal median-nerve enlargement in a young patient with acute motor axonal neuropathy

Clinical neurophysiology, 2017-09, Vol.128 (9), p.e251-e252

2017

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The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation

Ideggyógyászati szemle, 2014-11, Vol.67 (11-12), p.420

2014

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Genetics and present therapy options in Parkinson's disease: a review

Ideggyógyászati szemle, 2009-05, Vol.62 (5-6), p.155

2009

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The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients

Ideggyógyászati szemle, 2012-07, Vol.65 (7-8), p.239

2012

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Different Patterns of Nerve Enlargement in Polyneuropathy Subtypes as Detected by Ultrasonography

Ultrasound in medicine & biology, 2014-06, Vol.40 (6), p.1138-1145

2014

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MELAS syndrome mimicking somatoform disorder

Central European journal of medicine, 2011-12, Vol.6 (6), p.758-761

2011

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Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease

European journal of human genetics : EJHG, 2015-10, Vol.23 (10), p.1328-1333

2015

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Chronic high-frequency globus pallidus internus stimulation in different types of dystonia: A clinical, video, and MRI report of six patients presenting with segmental, cervical, and generalized dystonia

Movement disorders, 2002-01, Vol.17 (1), p.138-144

2002

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Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients

Neuromuscular disorders : NMD, 2016-10, Vol.26 (10), p.706-711

2016

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Mitochondrial DNA Mutations and Cognition: A Case-Series Report

Archives of clinical neuropsychology, 2014-06, Vol.29 (4), p.315-321

2014

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The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy

Clinical neuropathology, 2015-03, Vol.34 (2), p.89-95

2015

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Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson’s disease

Neurogenetics, 2012-08, Vol.13 (3), p.281-285

2012

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Rare variants in [beta]-Amyloid precursor protein (APP) and Parkinson's disease

European journal of human genetics : EJHG, 2015-10, Vol.23 (10), p.1328

2015

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DYT1 positive generalised dystonia: a case study of two siblings

Ideggyógyászati szemle, 2007-07, Vol.60 (7-8), p.342

2007

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The role of SCARB2 as susceptibility factor in P arkinson's disease

Movement disorders, 2013-04, Vol.28 (4), p.538-540

2013

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Therapie der multiplen Sklerose

Deutsche medizinische Wochenschrift, 2008-03, Vol.124 (19), p.595-599

2008

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Coexisting huntingtin and SCA8 repeat expansion: Case report of a severe complex neurodegenerative syndrome

Journal of the neurological sciences, 2010-06, Vol.293 (1), p.116-118

2010

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Guillain‐Barré syndrome during SARS‐CoV‐2 pandemic: A case report and review of recent literature

Ultrasonography of MADSAM neuropathy: Focal nerve enlargements at sites of existing and resolved conduction blocks

The role of SCARB2 as susceptibility factor in Parkinson's disease

Psychiatric symptoms of patients with primary mitochondrial DNA disorders

The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson’s Disease in the Hungarian Population

A susceptibility locus for Parkinson's disease maps to chromosome 2p13

Rare variants in PLXNA4 and Parkinson's disease

Guillain‐Barr é syndrome during SARS‐CoV ‐2 pandemic: A case report and review of recent literature

P228 Reversible axonal conduction blocks and sonographic distal median-nerve enlargement in a young patient with acute motor axonal neuropathy

The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation

Genetics and present therapy options in Parkinson's disease: a review

The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients

Different Patterns of Nerve Enlargement in Polyneuropathy Subtypes as Detected by Ultrasonography

MELAS syndrome mimicking somatoform disorder

Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease

Chronic high-frequency globus pallidus internus stimulation in different types of dystonia: A clinical, video, and MRI report of six patients presenting with segmental, cervical, and generalized dystonia

Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients

Mitochondrial DNA Mutations and Cognition: A Case-Series Report

The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson’s disease

Rare variants in [beta]-Amyloid precursor protein (APP) and Parkinson's disease

DYT1 positive generalised dystonia: a case study of two siblings

The role of SCARB2 as susceptibility factor in P arkinson's disease

Therapie der multiplen Sklerose

Coexisting huntingtin and SCA8 repeat expansion: Case report of a severe complex neurodegenerative syndrome

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