UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 47

Sortiert nach

Donor KIR2DS1 reduces the risk of transplant related mortality in HLA-C2 positive young recipients with hematological malignancies treated by myeloablative conditioning

PloS one, 2019-06, Vol.14 (6), p.e0218945-e0218945

2019

Volltextzugriff (PDF)

Similar Genetic Features and Different Islet Cell Autoantibody Pattern of Latent Autoimmune Diabetes in Adults (LADA) Compared With Adult-Onset Type 1 Diabetes With Rapid Progression

Diabetes care, 2003-02, Vol.26 (2), p.452-457

2003

Volltextzugriff (PDF)

The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosis

International immunology, 2006-11, Vol.18 (11), p.1585-1590

2006

Volltextzugriff (PDF)

Structural polymorphisms in the mannose-binding lectin gene are associated with juvenile idiopathic arthritis

Journal of rheumatology, 2009-04, Vol.36 (4), p.843

2009

Volltextzugriff (PDF)

HLA-association of serum levels of natural antibodies

Molecular immunology, 2009-04, Vol.46 (7), p.1416-1423

2009

Volltextzugriff (PDF)

Alloimmune and Autoimmune Background in Recurrent Pregnancy Loss - Successful Immunotherapy by Intravenous Immunoglobulin

American journal of reproductive immunology (1989), 2006-05, Vol.55 (5), p.331-340

2006

Volltextzugriff (PDF)

HLA-DR genotypes in familial rheumatoid arthritis: increased frequency of protective and neutral alleles in a multicase family

Journal of rheumatology, 2005-12, Vol.32 (12), p.2299

2005

Volltextzugriff (PDF)

Evaluating risk, safety and efficacy of novel reproductive techniques and therapies through the EuroGTP II risk assessment tool

Human reproduction (Oxford), 2020-08, Vol.35 (8), p.1821-1838

2020

Volltextzugriff (PDF)

Sex-specific survival difference in association with HLA-DRB1∗04 following allogeneic haematopoietic stem cell transplantation for lymphoid malignancies

Human immunology, 2018-01, Vol.79 (1), p.13-19

2018

Volltextzugriff (PDF)

Familial multiple myeloma. Two more families

Central European journal of medicine, 2009-12, Vol.4 (4), p.501-505

2009

Volltextzugriff (PDF)

Effective humoral immunity against diphtheria and tetanus in patients with systemic lupus erythematosus or myasthenia gravis

Molecular immunology, 2013-07, Vol.54 (3-4), p.453-456

2013

Volltextzugriff (PDF)

Frequency of Carriers of 8.1 Ancestral Haplotype and its Fragments in Two Caucasian Populations

Immunological investigations, 2007-01, Vol.36 (3), p.307-319

2007

Volltextzugriff (PDF)

Immunotherapy with intravenous immunoglobulin (IVIG) and with partner-specific thrombocyte (PST) for treatment of recurrent spontaneous abortions (RSA): Hungarian experience

Journal of reproductive immunology, 2014-03, Vol.101, p.35-36

2014

Volltextzugriff (PDF)

Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?

European journal of gastroenterology & hepatology, 2011-03, Vol.23 (3), p.238-244

2011

Volltextzugriff (PDF)

Role of HLA-DRB1 and PTPN22 genes in susceptibility to juvenile idiopathic arthritis in Hungarian patients

Clinical and experimental rheumatology, 2008-11, Vol.26 (6), p.1146

2008

Volltextzugriff (PDF)

Roma ethnicity and clinical outcomes in kidney transplant recipients

International urology and nephrology, 2012-06, Vol.44 (3), p.945-954

2012

Volltextzugriff (PDF)

Frequent occurrence of conserved extended haplotypes (CEHs) in two Caucasian populations

Molecular immunology, 2010-06, Vol.47 (10), p.1899-1904

2010

Volltextzugriff (PDF)

Seroprevalence of Helicobacter pylori in Central-European uraemic patients and its possible association with presence of HLA-DR12 allele

European journal of gastroenterology & hepatology, 2008-09, Vol.20 (9), p.906-911, Article 906

2008

Volltextzugriff (PDF)

Multiple sclerosis and the CTLA4 autoimmunity polymorphism CT60: no association in patients from Germany, Hungary and Poland

Multiple sclerosis, 2008-03, Vol.14 (2), p.153-158

2008

Volltextzugriff (PDF)

Autoimmune-associated HLA-B8-DR3 haplotypes in Asian Indians are unique in C4 complement gene copy numbers and HSP-2 1267A/G

Human immunology, 2008-09, Vol.69 (9), p.580-587

2008

Volltextzugriff (PDF)

A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern

Diabetes/metabolism research and reviews, 2009-02, Vol.25 (2), p.127-135

2009

Volltextzugriff (PDF)

Linkage analysis of the C4A/ C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population

Molecular immunology, 2009-08, Vol.46 (13), p.2623-2629

2009

Volltextzugriff (PDF)

HLA-DQ3 is a probable risk factor for CMV infection in high-risk kidney transplant patients

Nephrology, dialysis, transplantation, 2008-08, Vol.23 (8), p.2673-2678

2008

Volltextzugriff (PDF)

Studies on mechanisms of the strong association between low C4B gene copy number and cardiovascular morbidity/mortality: Cross-talk of two neighboring genes

Molecular immunology, 2007-09, Vol.44 (16), p.3918-3919

2007

Volltextzugriff (PDF)

1 – 25 von 47

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(44)
Mit Volltextzugriff
(37)

Publikationsform

Artikel
(44)
Buchkapitel
(3)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Donor KIR2DS1 reduces the risk of transplant related mortality in HLA-C2 positive young recipients with hematological malignancies treated by myeloablative conditioning

Similar Genetic Features and Different Islet Cell Autoantibody Pattern of Latent Autoimmune Diabetes in Adults (LADA) Compared With Adult-Onset Type 1 Diabetes With Rapid Progression

The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosis

Structural polymorphisms in the mannose-binding lectin gene are associated with juvenile idiopathic arthritis

HLA-association of serum levels of natural antibodies

Alloimmune and Autoimmune Background in Recurrent Pregnancy Loss - Successful Immunotherapy by Intravenous Immunoglobulin

HLA-DR genotypes in familial rheumatoid arthritis: increased frequency of protective and neutral alleles in a multicase family

Evaluating risk, safety and efficacy of novel reproductive techniques and therapies through the EuroGTP II risk assessment tool

Sex-specific survival difference in association with HLA-DRB1∗04 following allogeneic haematopoietic stem cell transplantation for lymphoid malignancies

Familial multiple myeloma. Two more families

Effective humoral immunity against diphtheria and tetanus in patients with systemic lupus erythematosus or myasthenia gravis

Frequency of Carriers of 8.1 Ancestral Haplotype and its Fragments in Two Caucasian Populations

Immunotherapy with intravenous immunoglobulin (IVIG) and with partner-specific thrombocyte (PST) for treatment of recurrent spontaneous abortions (RSA): Hungarian experience

Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?

Role of HLA-DRB1 and PTPN22 genes in susceptibility to juvenile idiopathic arthritis in Hungarian patients

Roma ethnicity and clinical outcomes in kidney transplant recipients

Frequent occurrence of conserved extended haplotypes (CEHs) in two Caucasian populations

Seroprevalence of Helicobacter pylori in Central-European uraemic patients and its possible association with presence of HLA-DR12 allele

Multiple sclerosis and the CTLA4 autoimmunity polymorphism CT60: no association in patients from Germany, Hungary and Poland

Autoimmune-associated HLA-B8-DR3 haplotypes in Asian Indians are unique in C4 complement gene copy numbers and HSP-2 1267A/G

A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern

The HLA 8.1 ancestral haplotype is strongly linked to the C allele of -429T>C promoter polymorphism of receptor of the advanced glycation endproduct (RAGE) gene. Haplotype-independent association of the -429C allele with high hemoglobinA1C levels in diabetic patients

Linkage analysis of the C4A/ C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population

HLA-DQ3 is a probable risk factor for CMV infection in high-risk kidney transplant patients

Studies on mechanisms of the strong association between low C4B gene copy number and cardiovascular morbidity/mortality: Cross-talk of two neighboring genes

Suchergebnisse filtern