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...

Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group

Haematologica (Roma), 2011-12, Vol.96 (12), p.1831-1837

2011

Volltextzugriff (PDF)

Risk factors for central venous catheter thrombotic complications in children and adolescents with cancer

Cancer, 2010-09, Vol.116 (17), p.4197-4205

2010

Volltextzugriff (PDF)

Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry

Haematologica (Roma), 2014-08, Vol.99 (8), p.1395-1402

2014

Volltextzugriff (PDF)

P818: NEXT GENERATION TARGETED SEQUENCING FOR ENHANCED GENOTYPING OF DIAMOND BLACKFAN ANEMIA IN ISRAEL

HemaSphere, 2022-06, Vol.6 (Suppl), p.712-713

2022

Volltextzugriff (PDF)

P817: SYNDROMES PREDISPOSING TO LEUKEMIA ARE A MAJOR CAUSE OF INHERITED CYTOPENIAS IN CHILDREN

HemaSphere, 2022-06, Vol.6 (Suppl), p.711-712

2022

Volltextzugriff (PDF)

P835: GENETIC BACKGROUND AND CLINICAL CHARACTERISTICS OF CONGENITAL NEUTROPENIAS IN ISRAEL

HemaSphere, 2022-06, Vol.6 (Suppl), p.729-730

2022

Volltextzugriff (PDF)

Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients

Journal of thrombosis and haemostasis, 2004-10, Vol.2 (10), p.1774-1781

2004

Volltextzugriff (PDF)

Reversal of cardiac complications in thalassemia major by long-term intermittent daily intensive iron chelation

European journal of haematology, 2003-06, Vol.70 (6), p.398-403

2003

Volltextzugriff (PDF)

Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I – response to Ahmed et al

British journal of haematology, 2006-05, Vol.133 (4), p.446-446

2006

Volltextzugriff (PDF)

Hints for writing a grant application

הרפואה, 2009-10, Vol.148 (10), p.728

2009

Volltextzugriff (PDF)

Multinational Study on the Clinical and Genetic Features of the ERCC6L2-Disease

BLOOD, 2021-11, Vol.138 (Supplement 1), p.864-864

2021

Volltextzugriff (PDF)

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

Cell, 2003-11, Vol.115 (4), p.461-473

2003

Volltextzugriff (PDF)

Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous arg1042trp mutation in codanin‐1)

European journal of haematology, 2008-03, Vol.80 (3), p.271-274

2008

Volltextzugriff (PDF)

The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet‐INNOCHRON COST Action

HemaSphere, 2023-04, Vol.7 (4), p.e872-n/a

2023

Volltextzugriff (PDF)

Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients

British journal of haematology, 2000-10, Vol.111 (1), p.338-343

2000

Volltextzugriff (PDF)

Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry

Haematologica (Roma), 2010-08, Vol.95 (8), p.1300-1307

2010

Volltextzugriff (PDF)

PS1269 AUTOIMMUNE NEUTROPENIA OF INFANCY‐ UNEXPECTED PREVALENCE OF PSEUDOMONAS SKIN INFECTIONS

HemaSphere, 2019-06, Vol.3 (S1), p.581-n/a

2019

Volltextzugriff (PDF)

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation

Blood, 2006-01, Vol.107 (1), p.334-340

2006

Volltextzugriff (PDF)

Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adults

European journal of haematology, 2002-03, Vol.68 (3), p.170-174

2002

Volltextzugriff (PDF)

CATSPER2, a human autosomal nonsyndromic male infertility gene

European journal of human genetics : EJHG, 2003-07, Vol.11 (7), p.497-502

2003

Volltextzugriff (PDF)

Neonatal manifestations of congenital dyserythropoietic anemia type I

The Journal of pediatrics, 1997-07, Vol.131 (1), p.95-97

1997

Volltextzugriff (PDF)

Expanding the clinical phenotype of autosomal dominant dyskeratosis congenita caused by TERT mutations

Haematologica (Roma), 2008-06, Vol.93 (6), p.943-944

2008

Volltextzugriff (PDF)

Hepatic iron overload: quantitative MR imaging

Radiology, 1991-05, Vol.179 (2), p.367-369

1991

Volltextzugriff (PDF)

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

European journal of haematology, 2005-02, Vol.74 (2), p.93-100

2005

Volltextzugriff (PDF)

1 – 25 von 93

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(79)
Mit Volltextzugriff
(66)

Publikationsform

Artikel
(92)
Berichte
(1)

Sprache

Englisch
(89)
Hebräisch
(4)

Erscheinungsjahr

n.n

Thema

Humans
(71)
Life Sciences & Biomedicine
(68)
Science & Technology
(68)
Hematology
(45)
Male
(43)
Biological And Medical Sciences
(42)
Medical Sciences
(42)
Female
(41)
Child
(37)
Hematologic And Hematopoietic Diseases
(33)
Adolescent
(28)
Adult
(26)
Child, Preschool
(23)
Pediatrics
(21)
Anemias. Hemoglobinopathies
(19)
Diseases Of Red Blood Cells
(19)
Infant
(15)
Mutation
(15)
Pedigree
(13)
Oncology
(12)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group

Risk factors for central venous catheter thrombotic complications in children and adolescents with cancer

Outcome and management of pregnancies in severe chronic neutropenia patients by the European Branch of the Severe Chronic Neutropenia International Registry

P818: NEXT GENERATION TARGETED SEQUENCING FOR ENHANCED GENOTYPING OF DIAMOND BLACKFAN ANEMIA IN ISRAEL

P817: SYNDROMES PREDISPOSING TO LEUKEMIA ARE A MAJOR CAUSE OF INHERITED CYTOPENIAS IN CHILDREN

P835: GENETIC BACKGROUND AND CLINICAL CHARACTERISTICS OF CONGENITAL NEUTROPENIAS IN ISRAEL

Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients

Reversal of cardiac complications in thalassemia major by long-term intermittent daily intensive iron chelation

Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I – response to Ahmed et al

Hints for writing a grant application

Multinational Study on the Clinical and Genetic Features of the ERCC6L2-Disease

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous arg1042trp mutation in codanin‐1)

The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia

The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet‐INNOCHRON COST Action

Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients

Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry

PS1269 AUTOIMMUNE NEUTROPENIA OF INFANCY‐ UNEXPECTED PREVALENCE OF PSEUDOMONAS SKIN INFECTIONS

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation

Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adults

CATSPER2, a human autosomal nonsyndromic male infertility gene

Neonatal manifestations of congenital dyserythropoietic anemia type I

Expanding the clinical phenotype of autosomal dominant dyskeratosis congenita caused by TERT mutations

Hepatic iron overload: quantitative MR imaging

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

Suchergebnisse filtern