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...

High D‐dimer level is associated with increased 15‐d and 3 months mortality through a more central localization of pulmonary emboli and serious comorbidity

British journal of haematology, 2008-01, Vol.140 (2), p.218-222

2008

Volltextzugriff (PDF)

Optimization of the diagnostic management of clinically suspected pulmonary embolism in hospitalized patients

British journal of haematology, 2014-12, Vol.167 (5), p.681-686

2014

Volltextzugriff (PDF)

C‐reactive protein and D‐dimer with clinical probability score in the exclusion of pulmonary embolism

British journal of haematology, 2005-08, Vol.130 (4), p.614-619

2005

Volltextzugriff (PDF)

Hb H disease in a Turkish family resulting from the interaction of a deletional α‐thalassaemia‐1 and a newly discovered poly A mutation

British journal of haematology, 1992-04, Vol.80 (4), p.527-532

1992

Volltextzugriff (PDF)

In vitro drug resistance profiles of adult versus childhood acute lymphoblastic leukaemia

British journal of haematology, 2000-09, Vol.110 (4), p.813-818

2000

Volltextzugriff (PDF)

The dominant β‐thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon (=arginine) at the 5′ end of the second exon

British journal of haematology, 1996-06, Vol.93 (4), p.841-844

1996

Volltextzugriff (PDF)

α and β thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization

British journal of haematology, 1994-02, Vol.86 (2), p.351-354

1994

Volltextzugriff (PDF)

Hb Icaria–Hb H disease: identification of the Hb Icaria mutation through analysis of amplified DNA

British journal of haematology, 1990-06, Vol.75 (2), p.250-253

1990

Volltextzugriff (PDF)

Sickle cell anaemia among Eti‐Turks: haematological, clinical and genetic observations

British journal of haematology, 1986-09, Vol.64 (1), p.45-55

1986

Volltextzugriff (PDF)

Dominant β‐thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β‐globin gene

British journal of haematology, 1991-10, Vol.79 (2), p.306-310

1991

Volltextzugriff (PDF)

Two different quadruplicated α globin gene arrangements

British journal of haematology, 1987-06, Vol.66 (2), p.245-250

1987

Volltextzugriff (PDF)

An IVS‐I‐117 (G→A) acceptor splice site mutation in the α 1‐globin gene is a nondeletional α‐thalassaemia‐2 determinant in an Indian population

British journal of haematology, 1993-09, Vol.85 (1), p.148-152

1993

Volltextzugriff (PDF)

γ‐mRNA and Hb F levels in β‐thalassaemia

British journal of haematology, 1994-10, Vol.88 (2), p.311-317

1994

Volltextzugriff (PDF)

Two different theta (θ) globin gene deletions observed among black newborn babies

British journal of haematology, 1988-02, Vol.68 (2), p.249-253

1988

Volltextzugriff (PDF)

Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β‐thalassaemia due to a homozygosity for the IVS‐I‐6 (T→C) mutation

British journal of haematology, 1994-04, Vol.86 (4), p.824-830

1994

Volltextzugriff (PDF)

Characterization of a newly discovered α‐thalassaemia‐1 in two Spanish patients with Hb H disease

British journal of haematology, 1988-12, Vol.70 (4), p.459-463

1988

Volltextzugriff (PDF)

The relative levels of βA and βS mRNAs in Hb S heterozygotes and in patients with Hb S‐β+ ‐thalassaemia or Hb S‐β+ ‐HPFH combinations

British journal of haematology, 1994-06, Vol.87 (2), p.353-356

1994

Volltextzugriff (PDF)

Variation in clinical severity among patients with Hb Lepore‐Boston‐β‐thalassaemia is related to the type of β‐thalassaemia

British journal of haematology, 1988-03, Vol.68 (3), p.351-355

1988

Volltextzugriff (PDF)

Decreased stability and structural heterogeneity of the residual platelet glycoprotein IIb/IIIa complex in a variant of Glanzmann's thrombasthenia

British journal of haematology, 1989-12, Vol.73 (4), p.514-521

1989

Volltextzugriff (PDF)

Red cell aggregation during normal pregnancy

British journal of haematology, 1988-01, Vol.68 (1), p.121-124

1988

Volltextzugriff (PDF)

The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence

British journal of haematology, 1989-11, Vol.73 (3), p.375-379

1989

Volltextzugriff (PDF)

Zeta and theta 1-globin gene deletions located on the same chromosome

British journal of haematology, 1989-11, Vol.73 (3), p.429

1989

Volltextzugriff (PDF)

Five haplotypes in Black β‐thalassaemia heterozygotes: three are associated with high and two with low Gγ values in fetal haemoglobin

British journal of haematology, 1985-02, Vol.59 (2), p.333-342

1985

Volltextzugriff (PDF)

A Second Type of Hereditary Persistence of Foetal Haemoglobin in India

British journal of haematology, 1973-07, Vol.25 (1), p.131-135

1973

Volltextzugriff (PDF)

Chemical Heterogeneity of Foetal Haemoglobin in the Lepore Haemoglobinopathy

British journal of haematology, 1974-06, Vol.27 (2), p.319-329

1974

Volltextzugriff (PDF)

1 – 25 von 26

Suche als RSS-Feed

Aktive Filter

KollektionSpringerLINK Contemporary (Konsortium Baden-Württemberg)

PublikationsformReviews

Zeitschrift / SerieBritish Journal Of Haematology

ThemaFemale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(26)
Mit Volltextzugriff
(4)

Publikationsform

Artikel
(26)

Sprache

Englisch
(26)

Erscheinungsjahr

n.n

Thema

Humans
(26)
Adult
(21)
Male
(21)
Biological And Medical Sciences
(16)
Medical Sciences
(16)
Child
(15)
Adolescent
(13)
Hematologic And Hematopoietic Diseases
(13)
Middle Aged
(13)
Hematology
(11)
Thalassemia - Genetics
(11)
Anemias. Hemoglobinopathies
(10)
Child, Preschool
(10)
Diseases Of Red Blood Cells
(10)
Globins - Genetics
(10)
Life Sciences & Biomedicine
(10)
Science & Technology
(10)
Base Sequence
(8)
Heterozygote
(8)

14 weitere anzeigen...

Weniger anzeigen...

Kollektion

Wiley Online Library
(26)
MEDLINE
(26)
Wiley Online Library Full Collection 2018
(26)
EZB Electronic Journals Library
(26)
WK Lippincott Williams & Wilkins–Connect here FIRST to enable access
(26)
IngentaConnect Journals
(1)

1 weiteren anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Br J Haematol
(3)
Br. J. Haematol
(1)

Menü

Weitere Dienste

Einstellungen

High D‐dimer level is associated with increased 15‐d and 3 months mortality through a more central localization of pulmonary emboli and serious comorbidity

Optimization of the diagnostic management of clinically suspected pulmonary embolism in hospitalized patients

C‐reactive protein and D‐dimer with clinical probability score in the exclusion of pulmonary embolism

Hb H disease in a Turkish family resulting from the interaction of a deletional α‐thalassaemia‐1 and a newly discovered poly A mutation

In vitro drug resistance profiles of adult versus childhood acute lymphoblastic leukaemia

The dominant β‐thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon (=arginine) at the 5′ end of the second exon

α and β thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization

Hb Icaria–Hb H disease: identification of the Hb Icaria mutation through analysis of amplified DNA

Sickle cell anaemia among Eti‐Turks: haematological, clinical and genetic observations

Dominant β‐thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β‐globin gene

Two different quadruplicated α globin gene arrangements

An IVS‐I‐117 (G→A) acceptor splice site mutation in the α 1‐globin gene is a nondeletional α‐thalassaemia‐2 determinant in an Indian population

γ‐mRNA and Hb F levels in β‐thalassaemia

Two different theta (θ) globin gene deletions observed among black newborn babies

Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β‐thalassaemia due to a homozygosity for the IVS‐I‐6 (T→C) mutation

Characterization of a newly discovered α‐thalassaemia‐1 in two Spanish patients with Hb H disease

The relative levels of βA and βS mRNAs in Hb S heterozygotes and in patients with Hb S‐β+ ‐thalassaemia or Hb S‐β+ ‐HPFH combinations

Variation in clinical severity among patients with Hb Lepore‐Boston‐β‐thalassaemia is related to the type of β‐thalassaemia

Decreased stability and structural heterogeneity of the residual platelet glycoprotein IIb/IIIa complex in a variant of Glanzmann's thrombasthenia

Red cell aggregation during normal pregnancy

The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence

Zeta and theta 1-globin gene deletions located on the same chromosome

Five haplotypes in Black β‐thalassaemia heterozygotes: three are associated with high and two with low Gγ values in fetal haemoglobin

A Second Type of Hereditary Persistence of Foetal Haemoglobin in India

Chemical Heterogeneity of Foetal Haemoglobin in the Lepore Haemoglobinopathy

Aktive Filter

Suchergebnisse filtern