(Q57122792)

severe congenital neutropenia

inferred from title

1 reference

C Ferry

1

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M Ouachée

2

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T Leblanc

3

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G Michel

4

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A Notz-Carrére

5

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R Tabrizi

6

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T Flood

7

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P Lutz

8

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A Fischer

9

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E Gluckman

10

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J Donadieu

Bone Marrow Transplantation

11

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language of work or name

English

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publication date

January 2005

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published in

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volume

35

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issue

1

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page(s)

45-50

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.bmt.1704718

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cites work

Infantile genetic agranulocytosis. A review with presentation of ten new cases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Mutations in proto-oncogene GFI1 cause human neutropenia and target ELA2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Severe chronic neutropenia: treatment and follow-up of patients in the Severe Chronic Neutropenia International Registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Uneventful outcome of unrelated hematopoietic stem cell transplantation in a patient with leukemic transformation of Kostmann syndrome and long‐lasting invasive pulmonary mycosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Correction of infantile agranulocytosis (Kostmann's syndrome) by allogeneic bone marrow transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Use of recombinant human granulocyte colony-stimulating factor to increase chemotherapy dose-intensity: a randomized trial in very high-risk childhood acute lymphoblastic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original "Kostmann family" and a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

7 January 2021

Effects of recombinant human granulocyte colony-stimulating factor on neutropenia in patients with congenital agranulocytosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

7 January 2021

Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French neutropenia register

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

7 January 2021

Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1704718

7 January 2021