Maria Judit Molnar

Summary

Publications

  1. doi request reprint [Significance of genetic tests in the era of personalized medicine]
    Judit Mária Molnár
    Genomikai Medicina és Ritka Betegségek Intézete, Semmelweis Egyetem, Budapest, Hungary
    Magy Onkol 57:16-20. 2013
  2. pmc Psychiatric symptoms of patients with primary mitochondrial DNA disorders
    Gabriella Inczédy-Farkas
    Clinical and Research Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary
    Behav Brain Funct 8:9. 2012
  3. doi request reprint Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population
    Zsuzsanna Pal
    Clinical and Research Centre for Molecular Neurology, Semmelweis University, Budapest, Hungary
    Hum Immunol 73:193-5. 2012
  4. doi request reprint A novel galectin-1 and interleukin 2 receptor β haplotype is associated with autoimmune myasthenia gravis
    Zsuzsanna Pal
    Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary
    J Neuroimmunol 229:107-11. 2010
  5. ncbi request reprint A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome
    Ildikó Vastagh
    Department of Neurology, Semmelweis University, Budapest
    Ideggyogy Sz 64:399-403. 2011
  6. doi request reprint Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: Association of galectin-8 (F19Y) occurrence with autoimmune diseases in a Caucasian population
    Zsuzsanna Pal
    Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary Department of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary
    Biochim Biophys Acta 1820:1512-8. 2012
  7. doi request reprint Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women
    Zsuzsanna Pal
    Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary
    Neuromuscul Disord 19:822-4. 2009
  8. doi request reprint Coexisting huntingtin and SCA8 repeat expansion: case report of a severe complex neurodegenerative syndrome
    Benjamin Bereznai
    Clinical and Research Center of Molecular Neurology, Semmelweis University, Budapest, Hungary
    J Neurol Sci 293:116-8. 2010

Collaborators

  • Aniko Gal
  • Benjamin Bereznai
  • Sabine Andre
  • Zsolt Illes
  • Ildikó Vastagh
  • Zsuzsanna Pal
  • Andras Falus
  • Edit Irén Buzás
  • Viktoria Remenyi
  • Judit Mária Molnár
  • Gabriella Inczédy-Farkas
  • Zsófia Varga
  • Gábor Hullám
  • Peter Antal
  • Hans Joachim Gabius
  • György Németh
  • Szilvia Magyarósi
  • Sanjeev Kumar Srivastava
  • Mihaly Svebis
  • Csilla Rozsa
  • Agnes Udvardy-Meszaros
  • Elena Gordeeva
  • Gyorgy Nagy
  • Petra Balla
  • Nicolai V Bovin
  • Csaba Szalai
  • Herbert Kaltner
  • Agnes F Semsei
  • Janos Gal
  • Agnes Semsei
  • Györgyi Soós
  • Sara Toth
  • Krisztina Pálóczi
  • András Millinghoffer
  • Attila Tordai

Detail Information

Publications8

  1. doi request reprint [Significance of genetic tests in the era of personalized medicine]
    Judit Mária Molnár
    Genomikai Medicina és Ritka Betegségek Intézete, Semmelweis Egyetem, Budapest, Hungary
    Magy Onkol 57:16-20. 2013
    ..Before approval such tests must be analytically and clinically validated. Broader use of these genetic tests is dependent on their price and reimbursement schemes...
  2. pmc Psychiatric symptoms of patients with primary mitochondrial DNA disorders
    Gabriella Inczédy-Farkas
    Clinical and Research Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary
    Behav Brain Funct 8:9. 2012
    ..The aim of our study was to assess psychiatric symptoms in patients with genetically proven primary mutation of the mitochondrial DNA...
  3. doi request reprint Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population
    Zsuzsanna Pal
    Clinical and Research Centre for Molecular Neurology, Semmelweis University, Budapest, Hungary
    Hum Immunol 73:193-5. 2012
    ..Our data suggest that the reduced responsiveness to interleukin-4 because the I75V polymorphism may contribute to the pathogenesis of myasthenia gravis...
  4. doi request reprint A novel galectin-1 and interleukin 2 receptor β haplotype is associated with autoimmune myasthenia gravis
    Zsuzsanna Pal
    Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary
    J Neuroimmunol 229:107-11. 2010
    ..Pathway analysis revealed interaction between LGALS1 and IL2Rβ suggesting a role of these proteins in this rare disease...
  5. ncbi request reprint A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome
    Ildikó Vastagh
    Department of Neurology, Semmelweis University, Budapest
    Ideggyogy Sz 64:399-403. 2011
    ..In young age onset of a stroke-like episode with undetermined etiology the mtDNA alterations always have to be excluded...
  6. doi request reprint Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: Association of galectin-8 (F19Y) occurrence with autoimmune diseases in a Caucasian population
    Zsuzsanna Pal
    Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary Department of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary
    Biochim Biophys Acta 1820:1512-8. 2012
    ..e. rheumatoid arthritis and myasthenia gravis...
  7. doi request reprint Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women
    Zsuzsanna Pal
    Center for Molecular Neurology, Department of Neurology, Semmelweis University, Budapest, Hungary
    Neuromuscul Disord 19:822-4. 2009
    ..We found no significant difference between any of the groups implying that these two polymorphisms probably do not play a role in the pathomechanism of myasthenia gravis in Caucasian women...
  8. doi request reprint Coexisting huntingtin and SCA8 repeat expansion: case report of a severe complex neurodegenerative syndrome
    Benjamin Bereznai
    Clinical and Research Center of Molecular Neurology, Semmelweis University, Budapest, Hungary
    J Neurol Sci 293:116-8. 2010
    ..We discuss phenotype-genotype correlation and the rule of triplet repeat expansions of gene ATXN8...