(Q34197725)

31 July 2017

title

Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I. (English)

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congenital dyserythropoietic anemia type I

31 July 2017

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6

Dorine W Swinkels

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31 July 2017

Hannah Tamary

1

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31 July 2017

Hanna Shalev

2

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31 July 2017

Galit Perez-Avraham

3

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31 July 2017

Meira Zoldan

4

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31 July 2017

Itai Levi

5

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31 July 2017

Toshihiko Tanno

7

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31 July 2017

Jeffery L Miller

8

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31 July 2017

language of work or name

English

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publication date

29 September 2008

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31 July 2017

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31 July 2017

volume

112

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31 July 2017

issue

13

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31 July 2017

page(s)

5241-5244

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Advances in quantitative hepcidin measurements by time-of-flight mass spectrometry

31 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Erythropoietin mediates hepcidin expression in hepatocytes through EPOR signaling and regulation of C/EBPalpha

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Regulation of hepcidin: insights from biochemical analyses on human serum samples

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Liver iron concentrations and urinary hepcidin in beta-thalassemia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Hepcidin in iron overload disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Dyserythropoiesis and congenital dyserythropoietic anaemias

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous Arg1042Trp mutation in codanin-1).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Hepcidin is decreased in TFR2 hemochromatosis

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2954708

Hepcidin and iron-loading anemias

28 October 2018

1 reference

12 December 2020

Hypocholesterolemia in chronic anemias with increased erythropoietic activity

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12 December 2020

Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts

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12 December 2020

Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I

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12 December 2020

Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis

1 reference

12 December 2020

Clinical and molecular variability in congenital dyserythropoietic anaemia type I

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12 December 2020

10.1182/BLOOD-2008-06-165738

Identifiers

DOI

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31 July 2017

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31 July 2017

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