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...

Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies

Clinical pediatrics, 2022-10, Vol.61 (9), p.629-644

2022

Volltextzugriff (PDF)

Containment of Local COVID-19 Outbreak Among Hematopoietic Stem Cell Transplant Recipients and Healthcare Workers in a Pediatric Stem Cell Unit

Journal of clinical immunology, 2021-10, Vol.41 (7), p.1523-1526

2021

Volltextzugriff (PDF)

Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

Blood, 2011-11, Vol.118 (19), p.5108-5118

2011

Volltextzugriff (PDF)

Langerhans cell histiocytosis of the cervical spine in a child: A case report and review of the literature

Pediatric hematology oncology journal, 2022-12, Vol.7 (4), p.161-164

2022

Volltextzugriff (PDF)

Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians

Cellular physiology and biochemistry, 2021-03, Vol.55 (1), p.117-129

2021

Volltextzugriff (PDF)

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

Frontiers in immunology, 2023-01, Vol.13, p.1057679-1057679

2023

Volltextzugriff (PDF)

PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA

HemaSphere, 2023-08, Vol.7 (S3), p.e0427349-n/a

2023

Volltextzugriff (PDF)

Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and Italy

Annals of human biology, 2019-11, Vol.46 (7-8), p.610-615

2019

Volltextzugriff (PDF)

FANCA Gene Mutations in North African Fanconi Anemia Patients

Frontiers in genetics, 2021-02, Vol.12, p.610050-610050

2021

Volltextzugriff (PDF)

Full Genome Characterization of Respiratory Syncytial Virus Causing a Fatal Infection in an Immunocompromised Patient in Tunisia

Pathogens (Basel), 2022-07, Vol.11 (7), p.758

2022

Volltextzugriff (PDF)

A membranous nephropathy in a 5 year-old boy: and if that’s not all? A nephrology quiz

Journal of nephrology, 2024-04, Vol.37 (3), p.821-825

2024

Volltextzugriff (PDF)

Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)

Clinical and molecular allergy CMA, 2012-04, Vol.10 (1), p.6-6, Article 6

2012

Volltextzugriff (PDF)

First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby

Journal of pediatric hematology/oncology, 2021-11, Vol.43 (8), p.e1055-e1058

2021

Volltextzugriff (PDF)

Incidence and risk factors for osteonecrosis of the femoral head in five hundred and ten sickle cell disease paediatric patients

International orthopaedics, 2023-12, Vol.47 (12), p.2941-2952

2023

Volltextzugriff (PDF)

Clinical features and predictors of osteoarticular manifestations in common variable immunodeficiency

Clinical rheumatology, 2023-11, Vol.42 (11), p.3123-3129

2023

Volltextzugriff (PDF)

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family

Annals of clinical biochemistry, 2023-03, Vol.60 (2), p.81-85

2023

Volltextzugriff (PDF)

Prevalence and predictive factors of splenic sequestration crisis among 423 pediatric patients with sickle cell disease in Tunisia

Blood cells, molecules, & diseases, 2020-02, Vol.80, p.102374-102374, Article 102374

2020

Volltextzugriff (PDF)

Successful Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide in a Severe Combined Immune Deficiency Patient: a First Report

Journal of clinical immunology, 2016-07, Vol.36 (5), p.437-440

2016

Volltextzugriff (PDF)

Predictors of autoimmune hemolytic anemia in beta-thalassemia patients with underlying red blood cells autoantibodies

Blood cells, molecules, & diseases, 2019-11, Vol.79, p.102342-102342, Article 102342

2019

Volltextzugriff (PDF)

Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency

Clinical infectious diseases, 2014-01, Vol.58 (2), p.204-213

2014

Volltextzugriff (PDF)

Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor beta 1 Deficiency

Clinical infectious diseases, 2014-01, Vol.58 (2), p.204-213

2014

Volltextzugriff (PDF)

Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell disease

Annals of hematology, 2018-11, Vol.97 (11), p.2261-2262

2018

Volltextzugriff (PDF)

Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study

Scandinavian journal of immunology, 2019-06, Vol.89 (6), p.e12763-n/a

2019

Volltextzugriff (PDF)

Myocardial and liver iron overload, assessed using T2 magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patients

Annals of hematology, 2017, Vol.96 (1), p.133-139

2017

Volltextzugriff (PDF)

1 – 25 von 83

Suche als RSS-Feed

Aktive Filter

KollektionTaylor & Francis

ThemaEngineering, Environmental

Nur zeigenGeprüft (Peer-Review)

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Mit Volltextzugriff
(75)

Publikationsform

Artikel
(82)
Tagungsberichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies

Containment of Local COVID-19 Outbreak Among Hematopoietic Stem Cell Transplant Recipients and Healthcare Workers in a Pediatric Stem Cell Unit

Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

Langerhans cell histiocytosis of the cervical spine in a child: A case report and review of the literature

Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)

PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA

Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and Italy

FANCA Gene Mutations in North African Fanconi Anemia Patients

Full Genome Characterization of Respiratory Syncytial Virus Causing a Fatal Infection in an Immunocompromised Patient in Tunisia

A membranous nephropathy in a 5 year-old boy: and if that’s not all? A nephrology quiz

Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)

First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby

Incidence and risk factors for osteonecrosis of the femoral head in five hundred and ten sickle cell disease paediatric patients

Clinical features and predictors of osteoarticular manifestations in common variable immunodeficiency

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family

Prevalence and predictive factors of splenic sequestration crisis among 423 pediatric patients with sickle cell disease in Tunisia

Successful Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide in a Severe Combined Immune Deficiency Patient: a First Report

Predictors of autoimmune hemolytic anemia in beta-thalassemia patients with underlying red blood cells autoantibodies

Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency

Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor beta 1 Deficiency

Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell disease

Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study

Myocardial and liver iron overload, assessed using T2 magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patients

Aktive Filter

Suchergebnisse filtern