Békés Megyei Pándy Kálmán Kórház

Research Output 1976 2017

2017
2 Citations (Scopus)

Synthesis, Structural Elucidation, Cyclic Voltammetry, and Theoretical Modelling of 2-Ferrocenyl-4H-benzo[e][1,3]thiazines and 2-Aryl-4H-ferroceno[e][1,3]thiazines

Fodor, K. J., Hegedüs, K., Csomós, P., Fodor, L., Gubán, D., Sohár, P. & Csámpai, A., 2017, In : European Journal of Inorganic Chemistry. 2017, 2, p. 511-520 10 p.

Research output: Article

Thiazines
Cyclic voltammetry
Ionization potential
Cyclization
Reducing Agents
1 Citation (Scopus)
Thiourea
Nuclear magnetic resonance spectroscopy
indole
phytoalexins
cyclobrassinin
2016
2 Citations (Scopus)
Indoles
Lactams
Imines
Cycloaddition
Silica Gel
1 Citation (Scopus)

Relevance of defensin β-2 and α defensins (HNP1-3) in Alzheimer's disease

Szekeres, M., Ivitz, E., Datki, Z., Kálmán, J., Pákáski, M., Várhelyi, Z. P., Klivényi, P., Zadori, D., Somogyvári, F., Szolnoki, Z., Vécsei, L. & Mándi, Y., máj. 30 2016, In : Psychiatry Research. 239, p. 342-345 4 p.

Research output: Article

Defensins
Gene Dosage
Cerebrospinal Fluid
Serum
Alzheimer disease, familial, type 3
2015
2 Citations (Scopus)

Decreased Number of Mitochondria in Leukoaraiosis

Szolnoki, Z., Szekeres, M., Szaniszlo, I., Balda, G., Bodor, A., Kondacs, A., Mándi, Y. & Somogyvári, F., nov. 1 2015, In : Archives of Medical Research. 46, 8, p. 604-608 5 p.

Research output: Article

Leukoaraiosis
Mitochondria
Free Radicals
Case-Control Studies
Leukocytes
1 Citation (Scopus)
Defensins
Genetic Polymorphisms
Multiple Sclerosis
Gene Dosage
DNA Copy Number Variations
5 Citations (Scopus)
Kynurenine
Parkinson Disease
Kynurenine 3-Monooxygenase
Single Nucleotide Polymorphism
Alleles
2013
72 Citations (Scopus)

Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: Systematic review and meta-analysis of 14 015 stroke cases and pooled analysis of primary biomarker data from up to 60 883 individuals

Khan, T. A., Shah, T., Prieto, D., Zhang, W., Price, J., Fowkes, G. R., Cooper, J., Talmud, P. J., Humphries, S. E., Sundstrom, J., Hubacek, J. A., Ebrahim, S., Lawlor, D. A., Ben-Shlomo, Y., Abdollahi, M. R., Slooter, A. J. C., Szolnoki, Z., Sandhu, M., Wareham, N., Frikke-Schmidt, R. & 29 others, Tybjærg-Hansen, A., Fillenbaum, G., Heijmans, B. T., Katsuya, T., Gromadzka, G., Singleton, A., Ferrucci, L., Hardy, J., Worrall, B., Rich, S. S., Matarin, M., Whittaker, J., Gaunt, T. R., Whincup, P., Morris, R., Deanfield, J., Donald, A., Smith, G. D., Kivimaki, M., Kumari, M., Smeeth, L., Khaw, K. T., Nalls, M., Meschia, J., Sun, K., Hui, R., Day, I., Hingorani, A. D. & Casas, J. P., ápr. 2013, In : International Journal of Epidemiology. 42, 2, p. 475-492 18 p.

Research output: Article

Apolipoproteins E
Meta-Analysis
Biomarkers
Stroke
Genotype
29 Citations (Scopus)

Association of vitamin D receptor gene polymorphisms and Parkinson's disease in Hungarians

Török, R., Török, N., Szalardy, L., Plangar, I., Szolnoki, Z., Somogyvari, F., Vecsei, L. & Klivenyi, P., szept. 13 2013, In : Neuroscience Letters. 551, p. 70-74 5 p.

Research output: Article

Calcitriol Receptors
Parkinson Disease
Genes
Nervous System Diseases
Gene Frequency
1 Citation (Scopus)

Hashimoto-encephalopathia

Pocsay, G., Gazdag, A., Engelhardt, J., Szaniszló, I., Szolnoki, Z., Forczek, G. & Mikló, L., aug. 1 2013, In : Orvosi Hetilap. 154, 33, p. 1312-1316 5 p.

Research output: Article

Iodide Peroxidase
Thyroid Diseases
Brain Diseases
Immunosuppressive Agents
Serum
7 Citations (Scopus)
Thiazines
Lactams
Stereoisomerism
Imines
Cycloaddition
2012
5 Citations (Scopus)

Evaluation of the MTHFR A1298C variant in leukoaraiosis

Szolnoki, Z., Szaniszlo, I., Szekeres, M., Hitri, K., Kondacs, A., Mándi, Y., Nedo, E. & Somogyvári, F., márc. 2012, In : Journal of Molecular Neuroscience. 46, 3, p. 492-496 5 p.

Research output: Article

Leukoaraiosis
Methylenetetrahydrofolate Reductase (NADPH2)
Homocysteine
Serum
Neuroimaging
9 Citations (Scopus)

Genetic polymorphisms of human β-defensins in patients with ischemic stroke

Tiszlavicz, Z., Somogyvári, F., Szolnoki, Z., Sztriha, L. K., Németh, B., Vécsei, L. & Mándi, Y., aug. 2012, In : Acta Neurologica Scandinavica. 126, 2, p. 109-115 7 p.

Research output: Article

Defensins
Genetic Polymorphisms
Stroke
Single Nucleotide Polymorphism
Gene Dosage
1 Citation (Scopus)
Lactams
Disulfides
Methanol
Thiazines
Derivatives
7 Citations (Scopus)
Isoquinolines
Lactams
Methanol
Indole Alkaloids
Sulfur
3 Citations (Scopus)
Thiazoles
Lactams
Sulfur
Extrusion
Isoquinolines
2011
9 Citations (Scopus)
Leukoaraiosis
Neuroimaging
Logistic Models
Mitochondrial Membrane Potential
Brain
202 Citations (Scopus)

Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: A meta-analysis of genetic studies and randomised trials

Holmes, M. V., Newcombe, P., Hubacek, J. A., Sofat, R., Ricketts, S. L., Cooper, J., Breteler, M. M., Bautista, L. E., Sharma, P., Whittaker, J. C., Smeeth, L., Fowkes, F. G. R., Algra, A., Shmeleva, V., Szolnoki, Z., Roest, M., Linnebank, M., Zacho, J., Nalls, M. A., Singleton, A. B. & 26 others, Ferrucci, L., Hardy, J., Worrall, B. B., Rich, S. S., Matarin, M., Norman, P. E., Flicker, L., Almeida, O. P., Van Bockxmeer, F. M., Shimokata, H., Khaw, K. T., Wareham, N. J., Bobak, M., Sterne, J. A. C., Smith, G. D., Talmud, P. J., Van Duijn, C., Humphries, S. E., Price, J. F., Ebrahim, S., Lawlor, D. A., Hankey, G. J., Meschia, J. F., Sandhu, M. S., Hingorani, A. D. & Casas, J. P., aug. 13 2011, In : The Lancet. 378, 9791, p. 584-594 11 p.

Research output: Article

Diet Therapy
Homocysteine
Folic Acid
Meta-Analysis
Stroke
30 Citations (Scopus)

EFNS guidelines for the molecular diagnosis of neurogenetic disorders: Motoneuron, peripheral nerve and muscle disorders

Burgunder, J. M., Schöls, L., Baets, J., Andersen, P., Gasser, T., Szolnoki, Z., Fontaine, B., Van Broeckhoven, C., Di Donato, S., De Jonghe, P., Lynch, T., Mariotti, C., Spinazzola, A., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Harbo, H. F. & Finsterer, J., febr. 2011, In : European Journal of Neurology. 18, 2, p. 207-217 11 p.

Research output: Article

Motor Neurons
Muscular Diseases
Peripheral Nerves
Molecular Biology
Genetic Testing
4 Citations (Scopus)
Thiazines
Derivatives
Sulfur
Nitrogen
Nuclear magnetic resonance
29 Citations (Scopus)
Roma
Haplotypes
Population
Gene Frequency
Restriction Fragment Length Polymorphisms
1 Citation (Scopus)

Ischaemiás stroke genetikai háttere: Hol tartunk most?

Maász, A., Szolnoki, Z., Balikó, L. & Melegh, B., márc. 1 2011, In : Orvosi Hetilap. 152, 12, p. 455-463 9 p.

Research output: Article

Stroke
Cerebrovascular Disorders
Precision Medicine
Heart Neoplasms
Genome-Wide Association Study

Molecular Diagnosis of Ataxias and Spastic Paraplegias

Gasser, T., Finsterer, J., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C. M. E., Zeviani, M., Burgunder, J. M. & Harbo, H. F., szept. 21 2011, European Handbook of Neurological Management. Wiley-Blackwell, Vol. 2. p. 73-85 13 p.

Research output: Chapter

Inborn Genetic Diseases
Paraplegia
Genetic Testing
Ataxia
Molecular Biology

Molecular Diagnosis of Channelopathies, Epilepsies, Migraine, Stroke and Dementias

Burgunder, J. M., Finsterer, J., Szolnoki, Z., Fontaine, B., Baets, J., Van Broeckhoven, C., Di Donato, S., De Jonghe, P., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Harbo, H. F. & Gasser, T., szept. 21 2011, European Handbook of Neurological Management. Wiley-Blackwell, Vol. 2. p. 87-96 10 p.

Research output: Chapter

Channelopathies
Migraine Disorders
Dementia
Epilepsy
Stroke

Molecular Diagnosis of Mitochondrial Disorders

Finsterer, J., Harbo, H. F., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Burgunder, J. M. & Gasser, T., szept. 21 2011, European Handbook of Neurological Management. Wiley-Blackwell, Vol. 2. p. 61-72 12 p.

Research output: Chapter

Mitochondrial Myopathies
Mitochondrial Diseases
Inborn Genetic Diseases
Molecular Biology

Molecular Diagnosis of Neurogenetic Disorders: General Issues, Huntington's Disease, Parkinson's Disease and Dystonias

Harbo, H. F., Finsterer, J., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Burgunder, J. M. & Gasser, T., szept. 21 2011, European Handbook of Neurological Management. Wiley-Blackwell, Vol. 2. p. 51-60 10 p.

Research output: Chapter

Dystonia
Huntington Disease
Parkinson Disease

Molecular Diagnosis of Neurogenetic Disorders: Motoneuron, Peripheral Nerve and Muscle Disorders

Burgunder, J. M., Schöls, L., Baets, J., Andersen, P., Gasser, T., Szolnoki, Z., Fontaine, B., Van Broeckhoven, C., Di Donato, S., De Jonghe, P., Lynch, T., Mariotti, C., Spinazzola, A., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Harbo, H. F. & Finsterer, J., szept. 21 2011, European Handbook of Neurological Management. Wiley-Blackwell, Vol. 2. p. 97-109 13 p.

Research output: Chapter

Motor Neurons
Muscular Diseases
Peripheral Nerves
2 Citations (Scopus)
2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide
Indoles
Isomers
Derivatives
Esters
18 Citations (Scopus)

Subcutaneous recombinant interferon-β-1a (Rebif®): A review of its use in the treatment of relapsing multiple sclerosis

Sanford, M., Lyseng-Williamson, K. A., Celius, E. G., Deisenhammer, F., Freedman, M. S., Hartung, H. P., Lam, R. & Szolnoki, Z., 2011, In : Drugs. 71, 14, p. 1865-1891 27 p.

Research output: Article

Interferons
Multiple Sclerosis
Placebos
Therapeutics
Costs and Cost Analysis
3 Citations (Scopus)
Triglycerides
Stroke
Alleles
Single Nucleotide Polymorphism
Restriction Fragment Length Polymorphisms
Alkaloids
Assays
Ethanol
Cells
Derivatives
2010
13 Citations (Scopus)
Thiazines
Lactams
Nuclear magnetic resonance spectroscopy
Methanol
Infrared spectroscopy
6 Citations (Scopus)

Annular desmotropy of three pairs of seven-membered heterocycles confirmed by X-ray crystallography

Holczbauer, T., Fábián, L., Csomós, P., Fodor, L. & Kálmán, A., jún. 2010, In : CrystEngComm. 12, 6, p. 1712-1717 6 p.

Research output: Article

Imines
X ray crystallography
imines
crystallography
Derivatives
7 Citations (Scopus)
Isoquinolines
Lactams
Isomerization
Nuclear magnetic resonance spectroscopy
Methanol
36 Citations (Scopus)

EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias

Gasser, T., Finsterer, J., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C. M. E., Zeviani, M., Burgunder, J. M. & Harbo, H. F., febr. 2010, In : European Journal of Neurology. 17, 2, p. 179-188 10 p.

Research output: Article

Paraplegia
Ataxia
Advisory Committees
Guidelines
Molecular Biology
13 Citations (Scopus)

EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias: EFNS GUIDELINES/CME ARTICLE

Burgunder, J. M., Finsterer, J., Szolnoki, Z., Fontaine, B., Baets, J., Van Broeckhoven, C., Di Donato, S., De Jonghe, P., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Harbo, H. F. & Gasser, T., máj. 2010, In : European Journal of Neurology. 17, 5, p. 641-648 8 p.

Research output: Article

Channelopathies
Migraine Disorders
Dementia
Epilepsy
Stroke
18 Citations (Scopus)
Column chromatography
Imines
Nuclear magnetic resonance spectroscopy
Chromatography
Infrared spectroscopy
19 Citations (Scopus)
Apolipoproteins
Regulator Genes
Triglycerides
Stroke
Genes
3 Citations (Scopus)
X ray analysis
Methanol
Nuclear magnetic resonance
Infrared radiation
Derivatives
2009
13 Citations (Scopus)
Multiple Sclerosis
Mitochondrial Membrane Potential
Mitochondria
Neuroimaging
Relapsing-Remitting Multiple Sclerosis
2 Citations (Scopus)
Myelin Basic Protein
Multiple Sclerosis
Single Nucleotide Polymorphism
Untranslated Regions
Neuroglia
47 Citations (Scopus)

EFNS guidelines on the molecular diagnosis of mitochondrial disorders

Finsterer, J., Harbo, H. F., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C. M. E., Zeviani, M., Burgunder, J. M. & Gasser, T., dec. 2009, In : European Journal of Neurology. 16, 12, p. 1255-1264 10 p.

Research output: Article

Mitochondrial Diseases
Guidelines
Molecular Biology
Genetic Databases
Molecular Pathology
47 Citations (Scopus)

EFNS guidelines on the molecular diagnosis of neurogenetic disorders: General issues, Huntington's disease, Parkinson's disease and dystonias

Harbo, H. F., Finsterer, J., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Burgunder, J. M. & Gasser, T., júl. 2009, In : European Journal of Neurology. 16, 7, p. 777-785 9 p.

Research output: Article

Dystonia
Huntington Disease
Parkinson Disease
Guidelines
Advisory Committees
4 Citations (Scopus)
Cerebrovascular Disorders
Genetic Polymorphisms
Polymorphism
Leukoaraiosis
Vascular Dementia
3 Citations (Scopus)
Kinesin
Stroke
Leukoaraiosis
Proteins
Neuroimaging
8 Citations (Scopus)

Galectin-2 3279TT variant protects against the lymphotoxin-α 252GG genotype associated ischaemic stroke

Szolnoki, Z., Maász, A., Magyari, L., Horvatovich, K., Farago, B., Kondacs, A., Bodor, A., Hadarits, F., Orosz, P., Ille, A. & Melegh, B., ápr. 2009, In : Clinical Neurology and Neurosurgery. 111, 3, p. 227-230 4 p.

Research output: Article

Galectin 2
Lymphotoxin-alpha
Homozygote
Stroke
Genotype