(Q36681614)

15 August 2017

Primary shunt hyperbilirubinaemia: a variant of the congenital dyserythropoietic anaemias (English)

1 reference

bilirubin metabolic disorder

15 August 2017

0 references

1 reference

Bird AR

1

1 reference

15 August 2017

Knottenbelt E

series ordinal

2

1 reference

15 August 2017

Jacobs P

series ordinal

3

1 reference

15 August 2017

Maigrot J

series ordinal

4

1 reference

15 August 2017

language of work or name

English

0 references

publication date

1 April 1991

1 reference

Postgraduate Medical Journal

15 August 2017

1 reference

15 August 2017

67

1 reference

15 August 2017

786

1 reference

15 August 2017

396-398

1 reference

Congenital dyserythropoietic anaemia: response to splenectomy and quantitation of ineffective erythropoiesis

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2398831

A new type of congenital dyserythropoietic anaemia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2398831

Role of bilirubin overproduction in revealing Gilbert's syndrome: is dyserythropoiesis an important factor?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2398831

Dyserythropoiesis and dyserythropoietic anemias.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2398831

Internal regulation of iron absorption

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2398831

Primary shunt hyperbilirubinemia with secondary iron overload: a case report

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2398831

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2398831

Congenital dyserythropoietic anemia—type IV

5 September 2018

1 reference

12 December 2020

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

12 December 2020

Type IV congenital dyserythropoietic anemia with an unusual response to splenectomy

1 reference

12 December 2020

Hereditary dyserythropoiesis with abnormal membrane folate transport

1 reference

12 December 2020

Iron loading in congenital dyserythropoietic anaemias and congenital sideroblastic anaemias

1 reference

12 December 2020

Identifiers

DOI

10.1136/PGMJ.67.786.396

1 reference

15 August 2017

1 reference

15 August 2017

1 reference