(Q50027819)

English

GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.

scientific article published on 21 March 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia. (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

1 reference

based on heuristic

inferred from title

author name string

Hiroyuki Ishida

1

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

Kosuke Imai

2

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

Kenichi Honma

3

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

Shin-Ichi Tamura

4

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

Toshihiko Imamura

5

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

Masafumi Ito

6

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

Shigeaki Nonoyama

7

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

publication date

21 March 2012

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

171

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

8

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

1273-1276

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

https://scigraph.springernature.com/pub.10.1007/s00431-012-1715-7

0 references

The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implications

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Immunity to microbes: lessons from primary immunodeficiencies.

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Successful allogeneic hematopoietic stem cell transplantation for GATA2 deficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

GATA-2 regulates granulocyte-macrophage progenitor cell function

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Prognostic significance of WT1 mRNA and anti-WT1 antibody levels in peripheral blood in patients with myelodysplastic syndromes.

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria, fungi, papillomaviruses, and myelodysplasia

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

Emberger syndrome-Primary lymphedema with myelodysplasia: Report of seven new cases

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1715-7

21 January 2018

The Wilms' tumor gene WT1 is a good marker for diagnosis of disease progression of myelodysplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22430350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-012-1715-7

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 February 2018

http://europepmc.org/abstract/MED/22430350

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