Laszlo Marodi

Summary

Affiliation: University of Debrecen
Country: Hungary

Publications

  1. ncbi request reprint Invasive Candida species disease in infants and children: occurrence, risk factors, management, and innate host defense mechanisms
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Curr Opin Pediatr 19:693-7. 2007
  2. doi request reprint Novel primary immunodeficiencies relevant to internal medicine: novel phenotypes
    L Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    J Intern Med 266:502-6. 2009
  3. pmc Molecular mechanisms of mucocutaneous immunity against Candida and Staphylococcus species
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    J Allergy Clin Immunol 130:1019-27. 2012
  4. doi request reprint The creation and progress of the J Project in Eastern and Central Europe
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Hungary
    Ann N Y Acad Sci 1238:65-73. 2011
  5. doi request reprint Primary immunodeficiencies may reveal potential infectious diseases associated with immune-targeting mAb treatments
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    J Allergy Clin Immunol 126:910-7. 2010
  6. ncbi request reprint Immunological and genetic bases of new primary immunodeficiencies
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, H 4, 012 Debrecen, Hungary
    Nat Rev Immunol 7:851-61. 2007
  7. ncbi request reprint Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease
    Melinda Erdos
    Department of Infectology and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Hum Mutat 25:506. 2005
  8. doi request reprint Novel dedicator of cytokinesis 8 mutations identified by multiplex ligation-dependent probe amplification
    Beáta Tóth
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Eur J Haematol 91:369-75. 2013
  9. ncbi request reprint Autoantibodies to IL-17A may be correlated with the severity of mucocutaneous candidiasis in APECED patients
    Adrien Katalin Sarkadi
    Department of Infectious and Pediatric Immunology, University of Debrecen, Medical and Health Science Center, Nagyerdei krt 98, 4032, Debrecen, Hungary
    J Clin Immunol 34:181-93. 2014
  10. ncbi request reprint Innate cellular immune responses in newborns
    Laszlo Marodi
    Department of Infectiology and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Nagyerdei krt 98, H 4012 Debrecen, Hungary
    Clin Immunol 118:137-44. 2006

Collaborators

Detail Information

Publications26

  1. ncbi request reprint Invasive Candida species disease in infants and children: occurrence, risk factors, management, and innate host defense mechanisms
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Curr Opin Pediatr 19:693-7. 2007
    ....
  2. doi request reprint Novel primary immunodeficiencies relevant to internal medicine: novel phenotypes
    L Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    J Intern Med 266:502-6. 2009
    ..Ground-breaking discoveries suggest that atypical haemolytic uraemic syndrome, Crohn's disease, and alveolar proteinosis may actually be manifestations of novel PIDs...
  3. pmc Molecular mechanisms of mucocutaneous immunity against Candida and Staphylococcus species
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    J Allergy Clin Immunol 130:1019-27. 2012
    ..Here we consider inborn errors of immunity arising from mutations in either STAT1 or STAT3 that affect mucocutaneous immunity to Candida and Staphylococcus species...
  4. doi request reprint The creation and progress of the J Project in Eastern and Central Europe
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Hungary
    Ann N Y Acad Sci 1238:65-73. 2011
    ....
  5. doi request reprint Primary immunodeficiencies may reveal potential infectious diseases associated with immune-targeting mAb treatments
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungary
    J Allergy Clin Immunol 126:910-7. 2010
    ....
  6. ncbi request reprint Immunological and genetic bases of new primary immunodeficiencies
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, University of Debrecen Medical and Health Science Center, H 4, 012 Debrecen, Hungary
    Nat Rev Immunol 7:851-61. 2007
    ....
  7. ncbi request reprint Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease
    Melinda Erdos
    Department of Infectology and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Hum Mutat 25:506. 2005
    ..These results suggest that a defect in ligand binding contributes to the loss of function of the SAP protein in patients carrying p.G16D mutation...
  8. doi request reprint Novel dedicator of cytokinesis 8 mutations identified by multiplex ligation-dependent probe amplification
    Beáta Tóth
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Eur J Haematol 91:369-75. 2013
    ..These data suggest that compound heterozygous del1-14 exons and del8-18 exons mutations result in a loss of function of DOCK8 protein and a typical DOCK8 deficiency phenotype...
  9. ncbi request reprint Autoantibodies to IL-17A may be correlated with the severity of mucocutaneous candidiasis in APECED patients
    Adrien Katalin Sarkadi
    Department of Infectious and Pediatric Immunology, University of Debrecen, Medical and Health Science Center, Nagyerdei krt 98, 4032, Debrecen, Hungary
    J Clin Immunol 34:181-93. 2014
    ..These data also suggest that the impaired release of IL-17-type cytokines by blood cells may be an element of the immunopathology of CMC in APECED patients. ..
  10. ncbi request reprint Innate cellular immune responses in newborns
    Laszlo Marodi
    Department of Infectiology and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Nagyerdei krt 98, H 4012 Debrecen, Hungary
    Clin Immunol 118:137-44. 2006
    ..A better understanding of innate immunity can make the development of techniques possible by which physicians more accurately tailor prevention and treatment of neonatal infections...
  11. doi request reprint Nijmegen breakage syndrome complicated with primary cutaneous tuberculosis
    Melinda Erdos
    Department of Infectious and Pediatric Immunology, University of Debrecen, Debrecen, Hungary
    Pediatr Infect Dis J 30:359-60. 2011
    ..This is the first report describing the simultaneous presentation of NBS and cutaneous tuberculosis...
  12. pmc Molecular genetic characterization of novel sphingomyelin phosphodiesterase 1 mutations causing niemann-pick disease
    Beáta Tóth
    Lysosomal Storage Disease Unit, Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Nagyerdei krt 98, 4032, Debrecen, Hungary
    JIMD Rep 3:125-9. 2012
    ..These data suggest that impaired protein stability and decreased enzyme activity are responsible for the disease in sphingomyelinase-deficient patients carrying the G247D and F572L mutations...
  13. doi request reprint Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome
    Vera Gulácsy
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Nagyerdei krt 98, 4032 Debrecen, Hungary
    Mol Immunol 48:788-92. 2011
    ..This report provides the first comprehensive overview of the molecular genetic and demographic features of WAS in ECE...
  14. doi request reprint Neuroendocrine carcinoma associated with X-linked hyper-immunoglobulin M syndrome: report of four cases and review of the literature
    Melinda Erdos
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Nagyerdei krt 98, H 4032 Debrecen, Hungary
    Clin Immunol 129:455-61. 2008
    ..We conclude that patients with XHIGM should be carefully followed to diagnose and treat NEC, a formidable neuroendocrine cancer...
  15. doi request reprint Novel sequence variation of AIRE and detection of interferon-omega antibodies in early infancy
    Beáta Tóth
    Department of Infectious and Pediatric Immunology, University of Debrecen, Medical and Health Science Center, Debrecen, Hungary
    Clin Endocrinol (Oxf) 72:641-7. 2010
    ..We wished to study clinical, immunological and genetic features of APS I in Hungarian patients, and to correlate anti-IFN-omega serum concentration with APS I and other multi-organ autoimmune diseases...
  16. doi request reprint Novel sequence variants of the alpha-galactosidase A gene in patients with Fabry disease
    Melinda Erdos
    Lysosomal Storage Disease Center, Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Nagyerdei krt 98, Debrecen, Hungary
    Mol Genet Metab 95:224-8. 2008
    ..This is the first comprehensive overview of molecular genetic features of Hungarian patients with FD...
  17. pmc New and recurrent gain-of-function STAT1 mutations in patients with chronic mucocutaneous candidiasis from Eastern and Central Europe
    Beáta Soltész
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary, EU
    J Med Genet 50:567-78. 2013
    ..Twelve of the 13 causal mutations described to date affect the coiled-coil domain (CCD) of STAT1. Several mutations, including R274W in particular, are recurrent, but the underlying mechanism is unclear...
  18. ncbi request reprint Genetically acquired class-switch recombination defects: the multi-faced hyper-IgM syndrome
    Melinda Erdos
    Department of Infectology and Pediatric Immunology, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary
    Immunol Lett 97:1-6. 2005
  19. doi request reprint The spread of the J Project
    Zsuzsa Horváth
    Department of Infectious and Pediatric Immunology, University of Debrecen, Medical and Health Science Center, Debrecen, Hungary
    J Clin Immunol 33:1037-42. 2013
    ..This paper highlights the achievements of the J Project and the spread of its concepts and spirit to the countries of Western Asia...
  20. ncbi request reprint Juvenile systemic sclerosis: a follow-up study of eight patients
    Szilvia Szamosi
    Third Department of Medicine, Division of Rheumatology, University of Debrecen Medical Center, 22 Moricz Zs Street, Debrecen, H 4004, Hungary
    Ann N Y Acad Sci 1051:229-34. 2005
    ..Also, the survival rate and final outcome of patients with jSSc appear to be better than those in patients with adult-onset SSc...
  21. pmc Neonatal innate immunity to infectious agents
    Laszlo Marodi
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Nagyerdei krt 98, H 4012 Debrecen, Hungary
    Infect Immun 74:1999-2006. 2006
  22. doi request reprint Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study
    Beáta Tóth
    Department of Infectious and Pediatric Immunology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Mol Immunol 46:2140-6. 2009
    ..This report provides the first comprehensive overview of the molecular genetic and demographic features of XLA in Eastern and Central Europe...
  23. doi request reprint Association of renal ectopia with Fabry's disease in 3 patients
    Eva Rakoczi
    Lysosomal Storage Disease Center, Department of Infectious and Pediatric Immunology, University of Debrecen, Debrecen, Hungary
    J Urol 181:1949-54. 2009
    ..We present clinical and genetic features in 2 female and 1 male patient with Fabry's disease and renal ectopia...
  24. ncbi request reprint Rebound hepatosplenomegaly in type 1 Gaucher disease
    Judit Toth
    Departments of Radiology, Medical and Health Science Center, University of Debrecen, Debrecen, Hungary
    Eur J Haematol 70:125-8. 2003
    ..This report suggests that cessation of ERT in Gaucher disease may result in severe and complicated rebound visceromegaly...
  25. ncbi request reprint Recurrent infection with genetically identical pneumococcal isolates in a patient with interleukin-1 receptor-associated kinase-4 deficiency
    Judit Szabo
    Department of Medical Microbiology, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary
    J Med Microbiol 56:863-5. 2007
    ..It is proposed that eradication of pneumococci from the nasopharynx, and immunization of household contacts may prevent recurrent infection in IRAK-4-deficient patients...
  26. ncbi request reprint Recurrent CXCR4 sequence variation in a girl with WHIM syndrome
    Krisztina Alapi
    Department of Infectious and Pediatric Immunology, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary
    Eur J Haematol 78:86-8. 2007
    ..1013C > G sequence variant suggesting WHIM syndrome. Recurrent c.1013C > G sequence variant of the CXCR4 gene resulting in p.S338X truncation mutation of this chemokine receptor protein is first reported here...