Hematopoietic stem cell transplantation in severe congenital neutropenia: experience of the French SCN register (Q57122792)

severe congenital neutropenia

inferred from title

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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

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

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

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

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

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

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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

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

21 January 2018

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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

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7 January 2021

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

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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

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7 January 2021

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

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7 January 2021