UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Living the SARS-CoV-2 pandemic in Turkey

Nature immunology, 2021-03, Vol.22 (3), p.260-260

Çağdaş, Deniz

2021

Volltextzugriff (PDF)

COVID-19 in Patients with Primary Immunodeficiency

Journal of clinical immunology, 2021-10, Vol.41 (7), p.1515-1522

2021

Volltextzugriff (PDF)

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function

Haematologica (Roma), 2019-03, Vol.104 (3), p.609-621

2019

Volltextzugriff (PDF)

A clinical score to guide in decision making for monogenic type I IFNopathies

Pediatric research, 2020-03, Vol.87 (4), p.745-752

2020

Volltextzugriff (PDF)

Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia

Odontology, 2021-04, Vol.109 (2), p.474-482

2021

Volltextzugriff (PDF)

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R

Haematologica (Roma), 2015-06, Vol.100 (6), p.e216-e219

2015

Volltextzugriff (PDF)

Expression of HLA class I and class II genes in patients with multiple skin warts

Experimental dermatology, 2021-11, Vol.30 (11), p.1642-1649

2021

Volltextzugriff (PDF)

A large single‐center cohort of bare lymphocyte syndrome: Immunological and genetic features in Turkey

Scandinavian journal of immunology, 2024-01, Vol.99 (1), p.e13335-n/a

2024

Volltextzugriff (PDF)

High Inborn Errors of Immunity Risk in Patients with Granuloma

Journal of clinical immunology, 2022-11, Vol.42 (8), p.1795-1809

2022

Volltextzugriff (PDF)

Clinical Features and HSCT Outcome for SCID in Turkey

Journal of clinical immunology, 2019-04, Vol.39 (3), p.316-323

2019

Volltextzugriff (PDF)

Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience

Journal of clinical immunology, 2021-07, Vol.41 (5), p.992-1003

2021

Volltextzugriff (PDF)

Inborn Errors of Immunity in Adults with Autoimmune Liver Diseases

The Turkish journal of gastroenterology, 2024-07, Vol.35 (7), p.560

2024

Volltextzugriff (PDF)

A single‐center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class‐ Switch Recombination defects

Scandinavian journal of immunology, 2022-11, Vol.96 (5), p.e13213-n/a

2022

Volltextzugriff (PDF)

Convalescent plasma and hyperimmune globulin therapy in COVID-19

Expert review of clinical immunology, 2021-04, Vol.17 (4), p.309-316

Cagdas, Deniz

2021

Volltextzugriff (PDF)

Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency

The Turkish journal of pediatrics, 2021-11, Vol.63 (6), p.1072-1077

2021

Volltextzugriff (PDF)

Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

Journal of clinical immunology, 2024-10, Vol.44 (7), p.157, Article 157

2024

Volltextzugriff (PDF)

A Patient Presenting with Chronic Mucocutaneous Candidiasis: A Novel IL12RB1 Mutation

Astım allerji immünoloji, 2022-12, Vol.20 (3), p.194-196

2022

Volltextzugriff (PDF)

Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study

Journal of clinical immunology, 2020-04, Vol.40 (3), p.494-502

2020

Volltextzugriff (PDF)

False Negative Next-Generation-Sequencing Analysis in a Lipopolysa ccharide-Responsive Beige-Like Anchor Defect

Turkish Archives of Pediatrics, 2024-03, Vol.59 (2), p.221-223

2024

Volltextzugriff (PDF)

ORAI1 defect in a patient with disseminated CMV infection and severe hypotonia

Turkish journal of pediatrics, 2023-07, Vol.65 (4), p.698-703

2023

Volltextzugriff (PDF)

Nutritional status of children with primary immunodeficiency: A single center experience

Pediatric investigation, 2022-01, Vol.64 (1), p.e14996-n/a

2022

Volltextzugriff (PDF)

Maternofetal Transfusion, Maternal Chimerism, and Maternal Engraftment: A Mystery in Health and Disease

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2021-11, Vol.9 (11), p.4154-4155

Cagdas, Deniz

2021

Volltextzugriff (PDF)

A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc

Journal of clinical immunology, 2014-11, Vol.34 (8), p.1009-1014

2014

Volltextzugriff (PDF)

DOCK8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection

Turkish journal of pediatrics, 2023-05, Vol.65 (3), p.536-541

2023

Volltextzugriff (PDF)

Impact of mannose‐binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children

Pediatric pulmonology, 2020-05, Vol.55 (5), p.1190-1198

2020

Volltextzugriff (PDF)

1 – 25 von 187

Suche als RSS-Feed

Aktive Filter

KollektionIngenta

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(140)
Mit Volltextzugriff
(133)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(7)

Menü

Weitere Dienste

Einstellungen

Living the SARS-CoV-2 pandemic in Turkey

COVID-19 in Patients with Primary Immunodeficiency

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function

A clinical score to guide in decision making for monogenic type I IFNopathies

Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R

Expression of HLA class I and class II genes in patients with multiple skin warts

A large single‐center cohort of bare lymphocyte syndrome: Immunological and genetic features in Turkey

High Inborn Errors of Immunity Risk in Patients with Granuloma

Clinical Features and HSCT Outcome for SCID in Turkey

Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience

Inborn Errors of Immunity in Adults with Autoimmune Liver Diseases

A single‐center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class‐ Switch Recombination defects

Convalescent plasma and hyperimmune globulin therapy in COVID-19

Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency

Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

A Patient Presenting with Chronic Mucocutaneous Candidiasis: A Novel IL12RB1 Mutation

Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study

False Negative Next-Generation-Sequencing Analysis in a Lipopolysa ccharide-Responsive Beige-Like Anchor Defect

ORAI1 defect in a patient with disseminated CMV infection and severe hypotonia

Nutritional status of children with primary immunodeficiency: A single center experience

Maternofetal Transfusion, Maternal Chimerism, and Maternal Engraftment: A Mystery in Health and Disease

A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc

DOCK8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection

Impact of mannose‐binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children

Aktive Filter

Suchergebnisse filtern