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...

Guidelines for the diagnosis and management of hereditary spherocytosis - 2011 update

British journal of haematology, 2012-01, Vol.156 (1), p.37-49

2012

Volltextzugriff (PDF)

Toward the harmonization of result presentation for the eosin‐5′‐maleimide binding test in the diagnosis of hereditary spherocytosis

Cytometry. Part B, Clinical cytometry, 2015-01, Vol.88 (1), p.50-57

2015

Volltextzugriff (PDF)

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

Nature genetics, 2005-11, Vol.37 (11), p.1258-1263

2005

Volltextzugriff (PDF)

Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis

American journal of hematology, 2017-10, Vol.92 (10), p.E607

2017

Volltextzugriff (PDF)

Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis

Cytometry. Part B, Clinical cytometry, 2008-07, Vol.74B (4), p.244-250

2008

Volltextzugriff (PDF)

Eosin‐5‐maleimide binding to band 3 and Rh‐related proteins forms the basis of a screening test for hereditary spherocytosis

British journal of haematology, 2004-01, Vol.124 (1), p.106-113

2004

Volltextzugriff (PDF)

Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia

British journal of haematology, 2000-12, Vol.111 (3), p.924-933

2000

Volltextzugriff (PDF)

Phenotype and mRNA Expression of Syncytiotrophoblast Microparticles Isolated from Human Placenta

Annals of the New York Academy of Sciences, 2008-08, Vol.1137 (1), p.144-147

2008

Volltextzugriff (PDF)

Hereditary spherocytosis

Paediatrics and child health, 2019-08, Vol.29 (8), p.359-364

2019

Volltextzugriff (PDF)

The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of ‘CDA type II’

Journal of clinical pathology, 2014-04, Vol.67 (4), p.367-369

2014

Volltextzugriff (PDF)

Hereditary spherocytosis

Paediatrics and child health, 2015-08, Vol.25 (8), p.381-386

2015

Volltextzugriff (PDF)

Rapid flow cytometric test for the diagnosis of membrane cytoskeleton‐associated haemolytic anaemia

British journal of haematology, 2000-12, Vol.111 (3), p.924-933

2000

Volltextzugriff (PDF)

Targeted next generation sequencing identifies a novel [beta]-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis

American journal of hematology, 2017-10, Vol.92 (10), p.E607

2017

Volltextzugriff (PDF)

Laboratory diagnosis of hereditary spherocytosis

Advances in Clinical Chemistry and Laboratory Medicine, 2012, p.88-90

2012

Volltextzugriff (PDF)

Blood group antigens on human erythrocytes-distribution, structure and possible functions

Biochimica et biophysica acta, 1994-04, Vol.1197 (1), p.15-44

King, May-Jean

1994

Volltextzugriff (PDF)

Towards the harmonization of result presentation for the eosin-5’- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosis: Feasibility of harmonizing EMA binding results

Cytometry. Part B, Clinical cytometry, 2014-09, p.n/a

2014

Volltextzugriff (PDF)

Two different glycosyltransferase defects that result in GalNAcα-O-peptide (Tn) expression

Glycobiology (Oxford), 1994-06, Vol.4 (3), p.267-280

1994

Volltextzugriff (PDF)

Structure and Possible Functional Significance of Human Red Cell Blood Group Antigens (ABH, Lewis, Ii, P-related, Duffy, and Antigens on Glycophorin A)

Trends in glycoscience and glycotechnology, 1991, Vol.3 (13), p.315-326

KING, May-Jean

1991

Volltextzugriff (PDF)

Hemolytic Anemias Associated with Disorders of Erythrocyte Membrane and Cytoskeleton Proteins

Laboratory Hematology Practice, 2012, p.602-614

2012

Volltextzugriff (PDF)

Absence of CD47 in protein 4.2–deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex

Blood, 2002-09, Vol.100 (5), p.1878-1885

2002

Volltextzugriff (PDF)

Towards the harmonization of result presentation for the eosin-5'- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosis

Cytometry. Part B, Clinical cytometry, 2014-09

2014

Volltextzugriff (PDF)

Structure and Possible Functional Significance of Human Red Cell Blood Group Antigens: ABH, Lewis, Ii, P-related, Duffy, and Antigens on Glycophorin A

Trends in Glycoscience and Glycotechnology, 1991/09/02, Vol.3(13), pp.315-326

KING, May-Jean

1991

Volltextzugriff (PDF)

Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis

Blood, 1998-12, Vol.92 (11), p.4481-4482

1998

Volltextzugriff (PDF)

ヒト赤血球の血液型抗原の構造と機能: ABH, ルイス, Ii, P関連, ダフィー, グリコホリンA

Trends in Glycoscience and Glycotechnology, 1991/09/02, Vol.3(13), pp.315-326

内川, 誠

1991

Volltextzugriff (PDF)

Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis

American journal of hematology, 2017, Vol.92 (10), p.E607-E609

2017

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(21)
Mit Volltextzugriff
(28)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Guidelines for the diagnosis and management of hereditary spherocytosis - 2011 update

Toward the harmonization of result presentation for the eosin‐5′‐maleimide binding test in the diagnosis of hereditary spherocytosis

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis

Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis

Eosin‐5‐maleimide binding to band 3 and Rh‐related proteins forms the basis of a screening test for hereditary spherocytosis

Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia

Phenotype and mRNA Expression of Syncytiotrophoblast Microparticles Isolated from Human Placenta

Hereditary spherocytosis

The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of ‘CDA type II’

Hereditary spherocytosis

Rapid flow cytometric test for the diagnosis of membrane cytoskeleton‐associated haemolytic anaemia

Targeted next generation sequencing identifies a novel [beta]-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis

Laboratory diagnosis of hereditary spherocytosis

Blood group antigens on human erythrocytes-distribution, structure and possible functions

Towards the harmonization of result presentation for the eosin-5’- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosis: Feasibility of harmonizing EMA binding results

Two different glycosyltransferase defects that result in GalNAcα-O-peptide (Tn) expression

Structure and Possible Functional Significance of Human Red Cell Blood Group Antigens (ABH, Lewis, Ii, P-related, Duffy, and Antigens on Glycophorin A)

Hemolytic Anemias Associated with Disorders of Erythrocyte Membrane and Cytoskeleton Proteins

Absence of CD47 in protein 4.2–deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex

Towards the harmonization of result presentation for the eosin-5'- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosis

Structure and Possible Functional Significance of Human Red Cell Blood Group Antigens: ABH, Lewis, Ii, P-related, Duffy, and Antigens on Glycophorin A

Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis

ヒト赤血球の血液型抗原の構造と機能: ABH, ルイス, Ii, P関連, ダフィー, グリコホリンA

Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis

Suchergebnisse filtern