Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis (Q34331072)

1 August 2017

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title

Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis (English)

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1 August 2017

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Fukuda MN

1

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1 August 2017

publication date

1 June 1993

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Best Practice and Research: Clinical Haematology

1 August 2017

published in

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1 August 2017

volume

6

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1 August 2017

issue

2

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1 August 2017

page(s)

493-511

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Alterations of Globin Chain Synthesis and of Red Cell Membrane Proteins in Congenital Dyserythropoietic Anemia I and II

1 August 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Congenital dyserythropoietic anaemia, types I and II: aberrant pattern of erythrocyte membrane proteins in CDA II, as revealed by two-dimensional polyacrylamide gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMP AS)

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Unclassified type of congenital dyserythropoietic anaemia (CDA) with prominent peripheral erythroblastosis

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Hereditary Erythroblastic Multinuclearity Associated with a Positive Acidified-Serum Test: a Type of Congenital Dyserythropoietic Anaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Normal serum ferritin levels in a patient with HEMPAS syndrome and iron overload

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS).

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Isolation and characterization of poly-N-acetyllactosaminylceramides accumulated in the erythrocytes of congenital dyserythropoietic anemia type II patients

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Congenital dyserythropoietic anaemia type II (HEMPAS): characterization of aberrant intracellular organelles by immunogold electron microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS)

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

AGGLUTINABILITY OF RED CELLS BY ANTI-I IN PATIENTS WITH THALASSEMIA MAJOR AND OTHER HAEMATOLOGICAL DISORDERS.

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Severe hemochromatosis: the predominant clinical manifestation of congenital dyserythropoietic anemia type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Erythrocyte membrane proteins in an unusual case of congenital dyserythropoietic anaemia type II (CDA II)

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Biliary proteins. Unique inhibitors of cholesterol crystal nucleation in human gallbladder bile

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Accumulation of glycolipids containing N-acetylglucosamine in erythrocyte stroma of patients with congenital dyserythropoietic anemia type II (HEMPAS)

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Immunochemistry of Ii-Active Glycosphingolipids of Erythrocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Congenital dyserythropoietic anaemia (CDA) with severe gout, rare Kell phenotype and erythrocyte, granulocyte and platelet membrane reduplication: a new variant of CDA type II.

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Incomplete glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (CDA II)

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Isolation, characterization, and expression of cDNAs encoding murine alpha-mannosidase II, a Golgi enzyme that controls conversion of high mannose to complex N-glycans

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Congenital dyserythropoietic anaemia type II (CDA-II): chromosomal banding studies and adherent cell effects on erythroid colony (CFU-E) and burst (BFU-E) formation

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II).

1 reference

https://api.crossref.org/works/10.1016%2FS0950-3536%2805%2980156-8

7 January 2021

10.1016/S0950-3536(05)80156-8

Identifiers

DOI

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1 August 2017

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