E. Sáfrány

发表

Interleukin-23 receptor gene variants in Hungarian systemic lupus erythematosus patients

L. Czirják, B. Melegh, M. Zeher, 2010, Inflammation Research.

Genetic variability and haplotype profile of MDR1 (ABCB1) in Roma and Hungarian population samples with a review of the literature.

B. Melegh, C. Sipeky, I. Takács, 2011, Drug metabolism and pharmacokinetics.

IGR2096a_1 T and IGR2198a_1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn’s disease in Hungarian patients

P. Orosz, Z. Tulassay, P. Sarlós, 2009, International Journal of Colorectal Disease.

[Possible role of selected IGR and SLC22A4/SLC22A5 loci in development of inflammatory bowel diseases].

P. Orosz, Z. Tulassay, P. Sarlós, 2009, Orvosi hetilap.

Prevalence of SLC22A4 1672T and SLC22A5 −207C combination defined TC haplotype in Hungarian ulcerative colitis patients

J. Bene, B. Melegh, B. Gasztonyi, 2007, Pathology & Oncology Research.

Vitamin K epoxide reductase complex 1 (VKORC1) haplotypes in healthy Hungarian and Roma population samples.

B. Melegh, N. Polgar, C. Sipeky, 2009, Pharmacogenomics.

[Pseudo-Bartter syndrome in a case of cystic fibrosis caused by C1529G and G3978A compound heterozygosity].

B. Melegh, E. Sulyok, P. Kisfali, 2008, Orvosi hetilap.

Difference of interleukin-23 receptor gene haplotype variants in ulcerative colitis compared to Crohn’s disease and psoriasis

Z. Tulassay, L. Kemény, B. Melegh, 2013, Inflammation Research.

Functional variants of interleukin-23 receptor gene confer risk for rheumatoid arthritis but not for systemic sclerosis

L. Czirják, B. Melegh, C. Sipeky, 2007, Annals of the rheumatic diseases.

Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome

B. Melegh, L. Markó, C. Sipeky, 2008, Pathology & Oncology Research.

Spinocerebellar Ataxia Type 2 (SCA2): Identification of Early Brain Degeneration in One Monozygous Twin in the Initial Disease Stage

T. Klockgether, U. Rüb, H. Korf, 2011, The Cerebellum.

Functional variants of the interleukin-23 receptor gene in non-gastrointestinal autoimmune diseases.

B. Melegh, E Safrany, B Melegh, 2009, Current medicinal chemistry.

Association of ARTS1 Gene Polymorphisms with Ankylosing Spondylitis in the Hungarian Population: The rs27044 Variant Is Associated with HLA-B*2705 Subtype in Hungarian Patients with Ankylosing Spondylitis

B. Pazár, P. Gergely, Z. Szekanecz, 2010, The Journal of Rheumatology.

Variants of the IL23R Gene are Associated with Ankylosing Spondylitis but not with Sjögren Syndrome in Hungarian Population Samples

B. Melegh, B. Pazár, M. Zeher, 2009, Scandinavian journal of immunology.

Functional Variants of Glucokinase Regulatory Protein and Apolipoprotein A5 Genes in Ischemic Stroke

B. Melegh, N. Polgar, C. Sipeky, 2010, Journal of Molecular Neuroscience.

Triglyceride level modifying functional variants of GALTN2 and MLXIPL in patients with ischaemic stroke

B. Melegh, N. Polgar, C. Sipeky, 2010, European journal of neurology.

GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness?

B. Melegh, N. Polgar, E. Fehér, 2010, Cardiovascular diabetology.

Interaction of the major inflammatory bowel disease susceptibility alleles in Crohn's disease patients.

P. Sarlós, J. Bene, B. Melegh, 2010, World journal of gastroenterology.

Triglyceride Level-Influencing Functional Variants of the ANGPTL3, CILP2, and TRIB1 Loci in Ischemic Stroke

B. Melegh, N. Polgar, C. Sipeky, 2011, NeuroMolecular Medicine.

Apolipoprotein A5 gene IVS3+G476A allelic variant confers susceptibility for development of ischemic stroke.

B. Melegh, C. Sipeky, P. Kisfali, 2008, Circulation journal : official journal of the Japanese Circulation Society.

Interaction between CTLA4 gene and IBD5 locus in Hungarian Crohn’s disease patients

P. Sarlós, J. Bene, B. Melegh, 2011, International Journal of Colorectal Disease.

ROLE OF INTERLEUKIN-23 RECEPTOR GENE POLYMORPHISMS IN AUTOIMMUNE AND IMMUNE MEDIATED DISEASES

B. Melegh, E. Sáfrány, 2010 .

[Mitochondrial DNA and its mutations: new advances in a new field].

B. Melegh, C. Sipeky, E. Sáfrány, 2007, Orvosi hetilap.

[The autosomal dominant cerebellar ataxias are hereditary neurodegenerative diseases].

B. Melegh, A. Guseo, E. Sáfrány, 2007, Orvosi hetilap.

Subtype in Hungarian Patients with Ankylosing Spondylitis Hungarian Population : The rs 27044 Variant Is Associated with HLA-B * 2705 Gene Polymorphisms with Ankylosing Spondylitis in the ARTS 1 Association

B. Pazár, P. Gergely, Z. Szekanecz, 2010 .

3′UTR C2370A allele of the IL-23 receptor gene is associated with relapsing-remitting multiple sclerosis

Z. Illés, B. Melegh, S. Komoly, 2008, Neuroscience Letters.

Polymorphisms of the IL23R Gene Are Associated with Psoriasis but not with Immunoglobulin A Nephropathy in a Hungarian Population

J. Nagy, L. Kemény, B. Melegh, 2011, Inflammation.

Variants of the IL23R Gene are Associated with Ankylosing Spondylitis but not with Sjögren Syndrome in Hungarian Population Samples

B. Melegh, B. Pazár, M. Zeher, 2009, Scandinavian journal of immunology.

Difference of interleukin-23 receptor gene haplotype variants in ulcerative colitis compared to Crohn’s disease and psoriasis

Z. Tulassay, L. Kemény, M. Széll, 2012, Inflammation Research.

Marked diversity of IL23R gene haplotype variants in rheumatoid arthritis comparing with Crohn’s disease and ankylosing spondylitis

L. Czirják, B. Melegh, B. Pazár, 2012, Molecular Biology Reports.