Year |
Citation |
Score |
2014 |
Reményi V, Inczédy-Farkas G, Gál A, Bereznai B, Pál Z, Karcagi V, Mechler F, Molnár MJ. The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation. Ideggyã³Gyã¡Szati Szemle. 67: 420-5. PMID 25720245 |
0.502 |
|
2014 |
Pal Z, Tóthfalusi L, Lörincz Z, György B, Molnar MJ, Falus A, Buzás EI. Immunosuppressants increase the levels of natural autoantibodies reactive with glycosaminoglycans in myasthenia gravis. Journal of Neuroimmunology. 276: 224-8. PMID 25139014 DOI: 10.1016/J.Jneuroim.2014.08.002 |
0.518 |
|
2013 |
Pál Z, Antal P, Srivastava S, Gál J, André S, Gordeeva E, Nagy G, Kaltner H, Bovin N, Molnár M, Falus A, Gabius H, Buzás E. A7.4 Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases Annals of the Rheumatic Diseases. 72: A49.1-A49. DOI: 10.1136/Annrheumdis-2013-203221.4 |
0.635 |
|
2012 |
Pál Z, Antal P, Srivastava SK, Hullám G, Semsei AF, Gál J, Svébis M, Soós G, Szalai C, André S, Gordeeva E, Nagy G, Kaltner H, Bovin NV, Molnár MJ, et al. Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: association of galectin-8 (F19Y) occurrence with autoimmune diseases in a Caucasian population. Biochimica Et Biophysica Acta. 1820: 1512-8. PMID 22683700 DOI: 10.1016/J.Bbagen.2012.05.015 |
0.603 |
|
2012 |
Pál Z, Varga Z, Semsei Ã, Reményi V, Rózsa C, Falus A, Illes Z, Buzás EI, Molnar MJ. Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population. Human Immunology. 73: 193-5. PMID 22119518 DOI: 10.1016/J.Humimm.2011.11.001 |
0.623 |
|
2011 |
Pál Z, Boczán J, Bereznai B, Lovas G, Molnár MJ. [Therapy for anti-MuSK antibody positive myasthenia gravis]. Orvosi Hetilap. 152: 1586-9. PMID 21920845 DOI: 10.1556/Oh.2011.29177 |
0.487 |
|
2010 |
Pál Z, Antal P, Millinghoffer A, Hullám G, Pálóczi K, Tóth S, Gabius HJ, Molnár MJ, Falus A, Buzás EI. A novel galectin-1 and interleukin 2 receptor β haplotype is associated with autoimmune myasthenia gravis. Journal of Neuroimmunology. 229: 107-11. PMID 20728947 DOI: 10.1016/J.Jneuroim.2010.07.015 |
0.6 |
|
2010 |
Gal A, Pentelenyi K, Remenyi V, Pal Z, Csanyi B, Tomory G, Rasko I, Molnar MJ. Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNA(Lys) associated with dystonia and stroke-like episodes. Acta Neurologica Scandinavica. 122: 252-6. PMID 19930207 DOI: 10.1111/J.1600-0404.2009.01297.X |
0.509 |
|
2009 |
Pal Z, Gal A, Remenyi V, Tordai A, Molnar MJ. Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women. Neuromuscular Disorders : Nmd. 19: 822-4. PMID 19793653 DOI: 10.1016/J.Nmd.2009.09.002 |
0.607 |
|
2009 |
Pál Z, Kiss E, Gál A, Csépány T, Lengyel A, Molnar MJ. Genetically determined neuropathy (CMT 1A) accompanied by immune dysfunction: a case report. Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]. 58: 359-61. PMID 19274435 DOI: 10.1007/S00011-009-0025-7 |
0.484 |
|
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