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...

Type I IFN–related NETosis in ataxia telangiectasia and Artemis deficiency

Journal of allergy and clinical immunology, 2018-07, Vol.142 (1), p.246-257

2018

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)

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)

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)

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)

Regulation of MYC by CARD14 in human epithelium is a determinant of epidermal homeostasis and disease

Cell reports (Cambridge), 2024-08, Vol.43 (8), p.114589, Article 114589

2024

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)

The effect of tibial slope angle on clinical and functional results after mobile bearing total knee arthroplasty

Journal of orthopaedics, trauma and rehabilitation, 2022-06, Vol.29 (1), p.221049172210758

2022

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)

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)

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)

Retroperitoneal Abscess in Severe Combined Immunodeficiency Probably Due to BCG Vaccine

Astım allerji immünoloji, 2020-08, Vol.18 (2), p.98-101

2020

Volltextzugriff (PDF)

The clinical and demographical characteristics of Turkish pediatric lymphedema patients: a multicenter study

Turkish journal of medical sciences, 2022-01, Vol.52 (4), p.1139-1147

2022

Volltextzugriff (PDF)

Mutation in BTK Gene Causing an Atypical Presentation of XLA

Astım allerji immünoloji, 2022-12, Vol.20 (3), p.197-201

2022

Volltextzugriff (PDF)

APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity

Scandinavian journal of immunology, 2023-08, Vol.98 (2), p.e13299-n/a

2023

Volltextzugriff (PDF)

A Novel Interleukin 17 Receptor A Mutation in a Child with Chronic Mucocutaneous Candidiasis and Staphylococcal Skin Infections

Turkish Archives of Pediatrics, 2023-07

2023

Volltextzugriff (PDF)

DiGeorge Syndrome: Simultaneously Diagnosis of A Mother-Baby Pair With Great Clinical Variability

Gazi tıp dergisi, 2022-04, Vol.33 (2), p.179-182

2022

Volltextzugriff (PDF)

Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species

Scientific reports, 2024-05, Vol.14 (1), p.10052-12, Article 10052

2024

Volltextzugriff (PDF)

A Rare Central Nervous System Involvement Due to CTLA-4 Gene Defect

Noro-Psikiyatri Arsivi, 2022-09, Vol.59 (3), p.248-252

2022

Volltextzugriff (PDF)

Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation

Turkish journal of haematology, 2015-12, Vol.32 (4), p.378-379

2015

Volltextzugriff (PDF)

Publisher Correction: Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species

Scientific reports, 2024-06, Vol.14 (1), p.14661-3, Article 14661

2024

Volltextzugriff (PDF)

1 – 25 von 102

Suche als RSS-Feed

Aktive Filter

KollektionEZB Electronic Journals Library

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(81)
Mit Volltextzugriff
(94)

Publikationsform

Artikel
(99)
Berichte
(3)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Type I IFN–related NETosis in ataxia telangiectasia and Artemis deficiency

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

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

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

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

Regulation of MYC by CARD14 in human epithelium is a determinant of epidermal homeostasis and disease

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

The effect of tibial slope angle on clinical and functional results after mobile bearing total knee arthroplasty

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

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

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

Retroperitoneal Abscess in Severe Combined Immunodeficiency Probably Due to BCG Vaccine

The clinical and demographical characteristics of Turkish pediatric lymphedema patients: a multicenter study

Mutation in BTK Gene Causing an Atypical Presentation of XLA

APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity

A Novel Interleukin 17 Receptor A Mutation in a Child with Chronic Mucocutaneous Candidiasis and Staphylococcal Skin Infections

DiGeorge Syndrome: Simultaneously Diagnosis of A Mother-Baby Pair With Great Clinical Variability

Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species

A Rare Central Nervous System Involvement Due to CTLA-4 Gene Defect

Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation

Publisher Correction: Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species

Aktive Filter

Suchergebnisse filtern