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E Endreffy

Showing results (11-20 of 25) with videos related to

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Acta Paediatrica Hungarica|January 1, 1992
Allele frequencies of cystic fibrosis-linked markers and F508 deletion in affected Hungarian familiesE Endreffy, K Burg, K Gyurkovits, et al.
Acta Biologica Hungarica|January 1, 1997
Molecular genetic studies in monogenic and polygenic human diseasesE Endreffy, László, A Szabó, et al.
European Neurology|February 19, 1999
Analysis of CAG repeat expansion in Huntington's disease gene (IT 15) in a Hungarian populationK Jakab, G Gárdián, E Endreffy, et al.
Acta Paediatrica Hungarica|January 1, 1992
About DR beta-restriction fragment length polymorphism (RFLP) analysis in kidney transplantation in connection with a paediatric patientE Endreffy, I B Petri, E Csajbók, et al.
Haematologia|January 1, 1993
DR beta-RFLP analysis of serologically DRw6 compatible kidney donor/recipient pairsE Endreffy, I B Petri, E Csajbók, et al.
Acta Physiologica Hungarica|April 21, 2007
Endothelin-1 gene and endothelial nitric oxide synthase gene polymorphisms in adolescents with juvenile and obesity-associated hypertensionA Baráth, E Endreffy, Cs Bereczki, et al.
Experimental and Clinical Immunogenetics|January 1, 1996
Molecular genetic analysis of HLA-DRB, -DQA, and -DQB polymorphisms in Hungarians and distribution of the DRB1*03 allele in adults and newbornsE Varga, E Endreffy, G Samu, et al.
Human Genetics|April 1, 1997
Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritisG Zsurka, J Ormos, B Iványi, et al.
Acta Microbiologica Et Immunologica Hungarica|November 1, 2000
Relationship between the occurrence of anti-SSA, anti-SSB autoantibodies and HLA class II alleles from the aspect of in vitro inhibitory effect of glucocorticosteroid on the antibody-dependent cellular cytotoxicity in patients with primary Sjögren's syndromeA Kovács, E Szekeres, L Berek, et al.
Journal of Inherited Metabolic Disease|January 7, 2004
Neonatal screening for biotinidase deficiency in Hungary: clinical, biochemical and molecular studiesA László, E A Schuler, E Sallay, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Acta Paediatrica Hungarica|January 1, 1992
Allele frequencies of cystic fibrosis-linked markers and F508 deletion in affected Hungarian familiesE Endreffy, K Burg, K Gyurkovits, et al.
Acta Biologica Hungarica|January 1, 1997
Molecular genetic studies in monogenic and polygenic human diseasesE Endreffy, László, A Szabó, et al.
European Neurology|February 19, 1999
Analysis of CAG repeat expansion in Huntington's disease gene (IT 15) in a Hungarian populationK Jakab, G Gárdián, E Endreffy, et al.
Acta Paediatrica Hungarica|January 1, 1992
About DR beta-restriction fragment length polymorphism (RFLP) analysis in kidney transplantation in connection with a paediatric patientE Endreffy, I B Petri, E Csajbók, et al.
Haematologia|January 1, 1993
DR beta-RFLP analysis of serologically DRw6 compatible kidney donor/recipient pairsE Endreffy, I B Petri, E Csajbók, et al.
Acta Physiologica Hungarica|April 21, 2007
Endothelin-1 gene and endothelial nitric oxide synthase gene polymorphisms in adolescents with juvenile and obesity-associated hypertensionA Baráth, E Endreffy, Cs Bereczki, et al.
Experimental and Clinical Immunogenetics|January 1, 1996
Molecular genetic analysis of HLA-DRB, -DQA, and -DQB polymorphisms in Hungarians and distribution of the DRB1*03 allele in adults and newbornsE Varga, E Endreffy, G Samu, et al.
Human Genetics|April 1, 1997
Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritisG Zsurka, J Ormos, B Iványi, et al.
Acta Microbiologica Et Immunologica Hungarica|November 1, 2000
Relationship between the occurrence of anti-SSA, anti-SSB autoantibodies and HLA class II alleles from the aspect of in vitro inhibitory effect of glucocorticosteroid on the antibody-dependent cellular cytotoxicity in patients with primary Sjögren's syndromeA Kovács, E Szekeres, L Berek, et al.
Journal of Inherited Metabolic Disease|January 7, 2004
Neonatal screening for biotinidase deficiency in Hungary: clinical, biochemical and molecular studiesA László, E A Schuler, E Sallay, et al.
Pageof 3