HEMPAS. Hereditary erythroblastic multinuclearity with positive acidified serum lysis test (Q33778425)

29 July 2017

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title

HEMPAS. Hereditary erythroblastic multinuclearity with positive acidified serum lysis test (English)

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29 July 2017

M N Fukuda

1

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29 July 2017

language of work or name

English

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publication date

1 October 1999

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Biochimica et Biophysica Acta

29 July 2017

published in

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29 July 2017

volume

1455

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29 July 2017

issue

2-3

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29 July 2017

page(s)

231-239

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

29 July 2017

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Congenital dyserythropoietic anemias

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7 January 2021

HEMPAS disease: genetic defect of glycosylation

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7 January 2021

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

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7 January 2021

Congenital dyserythropoietic anaemia type II associated with a new type of G6PD deficiency (G6PD Gabrovizza)

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Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child

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7 January 2021

Erythrocyte lipids and vitamin E in type II congenital dyserythropoietic anemia

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7 January 2021

Parvovirus infection associated with aplastic crisis in a patient with HEMPAS

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7 January 2021

Congenital dyserythropoietic anaemia (type II) presenting with haemosiderosis

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Transient anti-D in an Rh-positive patient with congenital dyserythropoietic anemia type II

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7 January 2021

Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)

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7 January 2021

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

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7 January 2021

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

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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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II

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7 January 2021

Molecular cloning and expression of cDNAs encoding human alpha-mannosidase II and a previously unrecognized alpha-mannosidase IIx isozyme

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7 January 2021

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

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7 January 2021

Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search

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7 January 2021

Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesis.

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7 January 2021

Mouse models of human genetic disease: which mouse is more like a man?

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7 January 2021

Gene targeting in the mouse

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7 January 2021

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

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7 January 2021

Polylactosamines are not obligate receptors for invasion of Plasmodium falciparum malaria as shown in HEMPAS variant II-gal- erythrocytes

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7 January 2021

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.

1 reference

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7 January 2021

Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25

1 reference

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7 January 2021

10.1016/S0925-4439(99)00070-8

Identifiers

DOI

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29 July 2017

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