Publications by authors named "Zoltan Maróti"

31Publications

Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1.

Brain Dev 2021 Jan 11;43(1):144-151. Epub 2020 Aug 11.

Department of Pediatrics, University of Szeged, Szeged, Hungary. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2020.07.015DOI Listing
January 2021

Childhood Obesity: Does it Have Any Effect on Young Arteries?

Front Pediatr 2020 16;8:389. Epub 2020 Jul 16.

Department of Pediatrics, Albert Szent-Györgyi Health Center, University of Szeged, Szeged, Hungary.

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http://dx.doi.org/10.3389/fped.2020.00389DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378393PMC
July 2020

Cerebrospinal Fluid Neurofilament Light Chain Is Associated with Kynurenine Pathway Metabolite Changes in Multiple Sclerosis.

Int J Mol Sci 2020 Apr 11;21(8). Epub 2020 Apr 11.

Department of Neurology, Faculty of Medicine, University of Szeged, Semmelweis u. 6., H-6725 Szeged, Hungary.

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http://dx.doi.org/10.3390/ijms21082665DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216195PMC
April 2020

Reference values for resting and post exercise hemodynamic parameters in a 6-18 year old population.

Sci Data 2020 01 21;7(1):26. Epub 2020 Jan 21.

Department of Pediatrics, University of Szeged Albert Szent-Györgyi Medical Center Faculty of Medicine, Szeged, Hungary.

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http://dx.doi.org/10.1038/s41597-020-0368-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972850PMC
January 2020

[Prevalence of hypertension in overweight and obese Hungarian children and adolescents].

Orv Hetil 2020 Jan;161(4):151-160

Szent-Györgyi Albert Klinikai Központ, Gyermekgyógyászati Klinika és Gyermekegészségügyi Központ, Szegedi Tudományegyetem Szeged, Korányi fasor 14-15., 6722.

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http://dx.doi.org/10.1556/650.2020.31543DOI Listing
January 2020

Cerebral cavernous malformation type 1 with retinal blood vessel tortuosity and KRIT1 gene mutation.

Ideggyogy Sz 2019 Jul;72(7-8):273-277

University of Pécs, School of Medicine, School of Graduate Studies, Pécs.

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http://dx.doi.org/10.18071/isz.72.0273DOI Listing
July 2019

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

Neurol Sci 2020 Jan 2;41(1):125-129. Epub 2019 Sep 2.

Genetic Diagnostic Laboratory, Department of Pediatrics and Pediatric Health Center, University of Szeged, Szeged, Korányi fasor 14-15, Szeged, H-6720, Hungary.

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http://dx.doi.org/10.1007/s10072-019-04044-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940312PMC
January 2020

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

Neurol Sci 2020 Jan 2;41(1):125-129. Epub 2019 Sep 2.

Genetic Diagnostic Laboratory, Department of Pediatrics and Pediatric Health Center, University of Szeged, Szeged, Korányi fasor 14-15, Szeged, H-6720, Hungary.

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http://dx.doi.org/10.1007/s10072-019-04044-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940312PMC
January 2020

A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.

J Appl Genet 2019 May 1;60(2):151-162. Epub 2019 Feb 1.

Department of Pediatrics, University of Szeged, Temesvári krt. 35-37, Szeged, 6726, Hungary.

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http://dx.doi.org/10.1007/s13353-019-00486-yDOI Listing
May 2019

Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis.

BMC Genomics 2018 Oct 29;19(1):778. Epub 2018 Oct 29.

Department of Pediatrics and Pediatric Health Center, Faculty of Medicine, University of Szeged, Szeged, Hungary.

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https://bmcgenomics.biomedcentral.com/articles/10.1186/s1286
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http://dx.doi.org/10.1186/s12864-018-5168-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206721PMC
October 2018

Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.

Pediatr Nephrol 2018 10 28;33(10):1713-1721. Epub 2018 Jun 28.

Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Nagyerdei krt. 98., Debrecen, Hungary.

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http://dx.doi.org/10.1007/s00467-018-3992-5DOI Listing
October 2018

Partial RAG deficiency in a patient with varicella infection, autoimmune cytopenia, and anticytokine antibodies.

J Allergy Clin Immunol Pract 2018 Sep - Oct;6(5):1769-1771.e2. Epub 2018 Feb 2.

Division of Pediatric Allergy & Immunology, Department of Pediatrics, University of South Florida, Tampa, Fla; Division of Pediatric Allergy Immunology, Massachusetts General Hospital for Children, Boston, Mass. Electronic address:

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http://dx.doi.org/10.1016/j.jaip.2018.01.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072614PMC
November 2019

Diffuse mesangial sclerosis in a PDSS2 mutation-induced coenzyme Q10 deficiency.

Pediatr Nephrol 2018 03 14;33(3):439-446. Epub 2017 Oct 14.

Department of Pediatrics and Pediatric Health Center, Faculty of Medicine, University of Szeged, Szeged, Hungary.

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http://dx.doi.org/10.1007/s00467-017-3814-1DOI Listing
March 2018

Diffuse mesangial sclerosis in a PDSS2 mutation-induced coenzyme Q10 deficiency.

Pediatr Nephrol 2018 03 14;33(3):439-446. Epub 2017 Oct 14.

Department of Pediatrics and Pediatric Health Center, Faculty of Medicine, University of Szeged, Szeged, Hungary.

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http://dx.doi.org/10.1007/s00467-017-3814-1DOI Listing
March 2018

Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation.

Cerebellum 2017 12;16(5-6):979-985

Department of Neurology, University of Szeged, Semmelweis u. 6, Szeged, H-6725, Hungary.

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http://dx.doi.org/10.1007/s12311-017-0870-9DOI Listing
December 2017

Novel frameshift mutation in the CHD7 gene associated with CHARGE syndrome with preaxial polydactyly.

Clin Dysmorphol 2016 Jul;25(3):98-100

Departments of aObstetrics and Gynecology bPediatrics cPathology, University of Szeged, Szeged, Hungary.

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http://dx.doi.org/10.1097/MCD.0000000000000120DOI Listing
July 2016

Changes in NADPH oxidase mRNA level can be detected in blood at inhaled corticosteroid treated asthmatic children.

Life Sci 2012 Nov 13;91(19-20):907-11. Epub 2012 Sep 13.

Department of Pediatrics and Child Health Center, Albert Szent-Györgyi Clinical Center, Faculty of Medicine, University of Szeged, H-6720 Szeged, Korányi fasor 14-15, Hungary.

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http://linkinghub.elsevier.com/retrieve/pii/S002432051200491
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http://dx.doi.org/10.1016/j.lfs.2012.08.039DOI Listing
November 2012

Genetic polymorphisms and the risk of progressive renal failure in elderly Hungarian patients.

Hemodial Int 2011 Oct 13;15(4):501-8. Epub 2011 Sep 13.

Szent Rókus Kórház Nephrológia Ambulancia, Baja, Hungary.

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http://dx.doi.org/10.1111/j.1542-4758.2011.00593.xDOI Listing
October 2011

Collagen type IV nephropathy: genetic heterogeneity examinations in affected Hungarian families.

Mol Cell Probes 2011 Feb 14;25(1):28-34. Epub 2010 Oct 14.

Department of Pediatrics and Child Health Center, H-6720 Szeged, Korányi fasor 14-15, Hungary.

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http://dx.doi.org/10.1016/j.mcp.2010.10.001DOI Listing
February 2011

Usefulness of combined genetic data in Hungarian families affected by autosomal dominant polycystic kidney disease.

Mol Cell Probes 2009 Feb 21;23(1):39-43. Epub 2008 Nov 21.

Pediatric Department and Pediatric Health Center, Faculty of Medicine, A. Szent-Györgyi Clinical Center, University of Szeged, Korányi fasor 14-15, H-6720 Szeged, Hungary.

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http://dx.doi.org/10.1016/j.mcp.2008.11.001DOI Listing
February 2009

Increased heme oxygenase-1 expression in premature infants with respiratory distress syndrome.

Eur J Pediatr 2008 Dec 27;167(12):1379-83. Epub 2008 Feb 27.

Department of Pediatrics, University of Szeged, Korányi fasor 14-15, Szeged, H-6720, Hungary.

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http://dx.doi.org/10.1007/s00431-008-0673-6DOI Listing
December 2008

Heme oxygenase-1 expression in premature and mature neonates during the first week of life.

Eur J Pediatr 2007 Oct 4;166(10):1033-8. Epub 2007 Jan 4.

Department of Pediatrics, University of Szeged, Faculty of Medicine, Albert Szent-Györgyi Medical and Pharmaceutical Center, Korányi fasor 14-15, 6725, Szeged, Hungary.

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http://dx.doi.org/10.1007/s00431-006-0375-xDOI Listing
October 2007

[Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].

Orv Hetil 2005 Dec;146(52):2647-53

Szegedi Tudományegyetem, Szent-Györgyi Albert Orvos es Gyógyszerésztudományi Centrum, Altalános Orvostudományi Kar, Gyermekgyógyászati Klinika es Gyermekegészségügyi Központ, Szeged.

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December 2005

Heme oxygenase 1 expression in young uremic patients on hemodialysis.

Pediatr Nephrol 2004 Apr 24;19(4):426-31. Epub 2004 Feb 24.

Department of Pediatrics, University of Szeged, Korányi fasor 14-15, 6725 Szeged, Hungary.

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http://dx.doi.org/10.1007/s00467-003-1384-xDOI Listing
April 2004