(Q33778425)

29 July 2017

1 reference

title

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

1 reference

29 July 2017

M N Fukuda

1

1 reference

PubMed ID

10571015

29 July 2017

language of work or name

English

0 references

publication date

1 October 1999

1 reference

Biochimica et Biophysica Acta

29 July 2017

1 reference

29 July 2017

1455

1 reference

29 July 2017

2-3

1 reference

29 July 2017

231-239

1 reference

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

29 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

Congenital dyserythropoietic anemias

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

HEMPAS disease: genetic defect of glycosylation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

Erythrocyte lipids and vitamin E in type II congenital dyserythropoietic anemia

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

Parvovirus infection associated with aplastic crisis in a patient with HEMPAS

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

Congenital dyserythropoietic anaemia (type II) presenting with haemosiderosis

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

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)

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

Gene targeting in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

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%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

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

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2899%2900070-8

7 January 2021

10.1016/S0925-4439(99)00070-8

Identifiers

DOI

1 reference

29 July 2017

1 reference

PubMed ID

10571015