Zsuzsanna Pal, Ph.D.

Affiliations: 
2011 Semmelweis Egyetem, Hungary 
Area:
Immunology
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"Zsuzsanna Pal"
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Parents

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Maria J. Molnar grad student 2011 Semmelweis Egyetem
 (Az antitest diverzifikaciot meghatarozo folyamatok, valamint egy autoantitestek altal medialt neuromuszkularis betegseg, a myasthenia gravis immunologiai es genetikai hatterenek vizsgalata.)
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Publications

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Reményi V, Inczédy-Farkas G, Gál A, et al. (2014) 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
Pal Z, Tóthfalusi L, Lörincz Z, et al. (2014) Immunosuppressants increase the levels of natural autoantibodies reactive with glycosaminoglycans in myasthenia gravis. Journal of Neuroimmunology. 276: 224-8
Pál Z, Antal P, Srivastava S, et al. (2013) A7.4 Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases Annals of the Rheumatic Diseases. 72: A49.1-A49
Pál Z, Antal P, Srivastava SK, et al. (2012) 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
Pál Z, Varga Z, Semsei Á, et al. (2012) Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population. Human Immunology. 73: 193-5
Pál Z, Boczán J, Bereznai B, et al. (2011) [Therapy for anti-MuSK antibody positive myasthenia gravis]. Orvosi Hetilap. 152: 1586-9
Pál Z, Antal P, Millinghoffer A, et al. (2010) A novel galectin-1 and interleukin 2 receptor β haplotype is associated with autoimmune myasthenia gravis. Journal of Neuroimmunology. 229: 107-11
Gal A, Pentelenyi K, Remenyi V, et al. (2010) Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNA(Lys) associated with dystonia and stroke-like episodes. Acta Neurologica Scandinavica. 122: 252-6
Pal Z, Gal A, Remenyi V, et al. (2009) Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women. Neuromuscular Disorders : Nmd. 19: 822-4
Pál Z, Kiss E, Gál A, et al. (2009) 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
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