UB Paderborn / Katalog / Suche / in CDI

1 – 23 von 23

Sortiert nach

Flow cytometric and functional characterization of AC133+ cells from human umbilical cord blood

British journal of haematology, 2000-03, Vol.108 (4), p.793-800

2000

Link zum Volltext

Verfügbarkeit prüfen

MLPA assay in F8 gene mutation screening

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-05, Vol.14 (3), p.625-627

2008

Link zum Volltext

Verfügbarkeit prüfen

Cyto-morphologic evaluation of bone marrow in infants with disseminated neuroblastoma

Journal of pediatric hematology/oncology, 2012-03, Vol.34 (2), p.154-158

2012

Link zum Volltext

Verfügbarkeit prüfen

Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A

European journal of human genetics : EJHG, 2005-05, Vol.13 (5), p.635-640

2005

Link zum Volltext

Verfügbarkeit prüfen

Duplication of exon 13 causes one third of the cases of mild hemophilia A in northern Italy

Haematologica (Roma), 2004-06, Vol.89 (6), p.758

2004

Link zum Volltext

Verfügbarkeit prüfen

Frequency of factor VIII intron 1 inversion in a cohort of severe hemophilia A Italian patients

Haematologica (Roma), 2003-05, Vol.88 (5), p.ELT17

2003

Link zum Volltext

Verfügbarkeit prüfen

Cyto-morphologic evaluation of bone marrow in infants with disseminated neuroblastoma

Journal of pediatric hematology/oncology, 2012-03, Vol.34 (2), p.154-158

2012

Link zum Volltext

Verfügbarkeit prüfen

Analysis of 18 novel mutations in the factor VIII gene

British journal of haematology, 2003-09, Vol.122 (5), p.810-817

2003

Link zum Volltext

Verfügbarkeit prüfen

Ectopic mRNA analysis and molecular modelling substantiate severe haemophilia in a patient with a FVIII gene splice mutation

Thrombosis and haemostasis, 2005, Vol.93 (2), p.391

2005

Link zum Volltext

Verfügbarkeit prüfen

Exon skipping partially restores factor VIII coagulant activity in patients with mild hemophilia A with exon 13 duplication

Haematologica (Roma), 2005-07, Vol.90 (7), p.997-999

2005

Link zum Volltext

Verfügbarkeit prüfen

Small FVIII gene rearrangements in 18 hemophilia A patients: Five novel mutations

American journal of hematology, 2005-02, Vol.78 (2), p.117-122

2005

Link zum Volltext

Verfügbarkeit prüfen

Flow cytometric and functional characertization of AC133+ cells from human umbilical cord blood

British journal of haematology, 2000-03, Vol.108 (4), p.793

2000

Link zum Volltext

Verfügbarkeit prüfen

Identification of mutations in exon 14 including five novelties in 13 Italian patients with haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-11, Vol.10 (6), p.744-746

2004

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis impact on the genetic counseling of sporadic hemophilia B families

American journal of medical genetics, 2003-05, Vol.118A (4), p.328-331

2003

Link zum Volltext

Verfügbarkeit prüfen

Growth factors increase retroviral transduction but decrease clonogenic potential of umbilical cord blood CD34+ cells

Haematologica (Roma), 1998-07, Vol.83 (7), p.580

1998

Link zum Volltext

Verfügbarkeit prüfen

Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhGM-CSF) and rhG-CSF in the Treatment of a Child With Severe Chronic Neutropenia

Blood, 1994-11, Vol.84 (9), p.3244-3245

1994

Link zum Volltext

Verfügbarkeit prüfen

A PEDIATRIC CASE OF PURE RED CELL APLASIA: SUCCESSFUL TREATMENT WITH ANTI‐LYMPHOCYTE GLOBULIN AND CORRELATION WITH IN VITRO T CELL‐MEDIATED INHIBITION OF ERYTHROPOIESIS

British journal of haematology, 1991-09, Vol.79 (1), p.129-130

1991

Link zum Volltext

Verfügbarkeit prüfen

Chronic childhood neutropenia: studies on the in vitro clonogenicity of bone marrow myeloid progenitors

Acta haematologica, 1991, Vol.86 (2), p.61

1991

Link zum Volltext

Verfügbarkeit prüfen

T and B Cells in Cerebrospinal Fluid in Acute Lymphocytic Leukemias

The New England journal of medicine, 1976-03, Vol.294 (10), p.550-551

1976

Link zum Volltext

Verfügbarkeit prüfen

Acute lymphoblastic leukemia in Noonan syndrome: Report of two cases

Medical and pediatric oncology, 1993, Vol.21 (6), p.454-455

1993

Link zum Volltext

Verfügbarkeit prüfen

Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome

American journal of medical genetics, 1999-11, Vol.87 (1), p.36-39

1999

Link zum Volltext

Verfügbarkeit prüfen

Secondary acute promyelocytic leukemia with t(8;21) and t(9;22) at onset and loss of the philadelphia chromosome at relapse

Cancer genetics and cytogenetics, 1990-07, Vol.47 (1), p.41-46

1990

Link zum Volltext

Verfügbarkeit prüfen

Immune evaluation of 50 children with neuroblastoma at onset

Medical and pediatric oncology, 1982, Vol.10 (4), p.321-330

1982

Link zum Volltext

Verfügbarkeit prüfen

1 – 23 von 23

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(19)
Mit Volltextzugriff
(17)

Publikationsform

Artikel
(23)

Sprache

Englisch
(23)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Humans
(20)
Life Sciences & Biomedicine
(15)
Science & Technology
(15)
Hematology
(12)
Female
(10)
Male
(10)
Hemophilia A - Genetics
(9)
Biological And Medical Sciences
(8)
Factor Viii - Genetics
(8)
Medical Sciences
(8)
Child
(6)
Child, Preschool
(5)
Hematologic And Hematopoietic Diseases
(5)
Infant
(5)
Italy
(5)
Genetics & Heredity
(4)
Mutation
(4)
Platelet Diseases And Coagulopathies
(4)
Bone Marrow - Pathology
(3)
Cells, Cultured
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Flow cytometric and functional characterization of AC133+ cells from human umbilical cord blood

MLPA assay in F8 gene mutation screening

Cyto-morphologic evaluation of bone marrow in infants with disseminated neuroblastoma

Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A

Duplication of exon 13 causes one third of the cases of mild hemophilia A in northern Italy

Frequency of factor VIII intron 1 inversion in a cohort of severe hemophilia A Italian patients

Cyto-morphologic evaluation of bone marrow in infants with disseminated neuroblastoma

Analysis of 18 novel mutations in the factor VIII gene

Ectopic mRNA analysis and molecular modelling substantiate severe haemophilia in a patient with a FVIII gene splice mutation

Exon skipping partially restores factor VIII coagulant activity in patients with mild hemophilia A with exon 13 duplication

Small FVIII gene rearrangements in 18 hemophilia A patients: Five novel mutations

Flow cytometric and functional characertization of AC133+ cells from human umbilical cord blood

Identification of mutations in exon 14 including five novelties in 13 Italian patients with haemophilia A

Mutation analysis impact on the genetic counseling of sporadic hemophilia B families

Growth factors increase retroviral transduction but decrease clonogenic potential of umbilical cord blood CD34+ cells

Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor (rhGM-CSF) and rhG-CSF in the Treatment of a Child With Severe Chronic Neutropenia

A PEDIATRIC CASE OF PURE RED CELL APLASIA: SUCCESSFUL TREATMENT WITH ANTI‐LYMPHOCYTE GLOBULIN AND CORRELATION WITH IN VITRO T CELL‐MEDIATED INHIBITION OF ERYTHROPOIESIS

Chronic childhood neutropenia: studies on the in vitro clonogenicity of bone marrow myeloid progenitors

T and B Cells in Cerebrospinal Fluid in Acute Lymphocytic Leukemias

Acute lymphoblastic leukemia in Noonan syndrome: Report of two cases

Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome

Secondary acute promyelocytic leukemia with t(8;21) and t(9;22) at onset and loss of the philadelphia chromosome at relapse

Immune evaluation of 50 children with neuroblastoma at onset

Suchergebnisse filtern