(Q50174928)

26 February 2018

title

A case of congenital dyserythropoietic anemia type II, Gilbert's syndrome and malleolar trophic ulcers. (English)

1 reference

26 February 2018

congenital dyserythropoietic anemia

main subject

1 reference

based on heuristic

inferred from title

congenital dyserythropoietic anemia type II

1 reference

3

Roberto Guariglia

1 reference

26 February 2018

Angelo Tirelli

6

object named as

Angelo Tirelli

1 reference

26 February 2018

author name string

Bruno Bordi

1

1 reference

26 February 2018

Maria Rosaria D'Amico

2

1 reference

26 February 2018

Gaetana Capobianco

4

1 reference

26 February 2018

Emilio Bordi

5

1 reference

26 February 2018

publication date

1 June 2002

1 reference

26 February 2018

published in

Hematology

1 reference

26 February 2018

volume

7

1 reference

26 February 2018

page(s)

197-199

1 reference

26 February 2018

issue

3

1 reference

26 February 2018

Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data

cites work

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II).

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

Natural history of congenital dyserythropoietic anemia type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

The congenital dyserythropoietic anaemias

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F1024533021000008146

10.1080/1024533021000008146

21 January 2018

Identifiers

DOI

1 reference

26 February 2018

PubMed ID

12243985

1 reference

26 February 2018