(Q34720883)

4 August 2017

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title

Successful treatment of Griscelli syndrome with unrelated donor allogeneic hematopoietic stem cell transplantation (English)

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stem cell transplantation

4 August 2017

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1 reference

M Aricò

1

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4 August 2017

M Zecca

2

1 reference

4 August 2017

N Santoro

3

1 reference

4 August 2017

D Caselli

4

1 reference

4 August 2017

R Maccario

5

1 reference

4 August 2017

C Danesino

6

1 reference

4 August 2017

G de Saint Basile

7

1 reference

4 August 2017

F Locatelli

8

1 reference

4 August 2017

language of work or name

English

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publication date

1 June 2002

1 reference

Bone Marrow Transplantation

4 August 2017

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4 August 2017

29

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4 August 2017

995-998

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4 August 2017

12

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https://scigraph.springernature.com/pub.10.1038/sj.bmt.1703567

4 August 2017

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cites work

A syndrome associating partial albinism and immunodeficiency

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Two genes are responsible for Griscelli syndrome at the same 15q21 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Griscelli syndrome: rare neonatal syndrome of recurrent hemophagocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Griscelli syndrome: report of the first peripheral blood stem cell transplant and the role of mutations in the RAB27A gene as an indication for BMT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Pathogenesis of haemophagocytic lymphohistiocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

Umbilical cord blood transplants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

A kindred with Griscelli disease: spectrum of neurological involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Partial albinism with immunodeficiency (Griscelli syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Bone marrow transplantation (BMT) for the syndrome of pigmentary dilution and lymphohistiocytosis (Griscelli's syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Griscelli syndrome: report of a case and review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvement

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Total body irradiation, thiotepa, and cyclophosphamide as a conditioning regimen for children with acute lymphoblastic leukemia in first or second remission undergoing bone marrow transplantation with HLA-identical siblings

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Fludarabine-based non-myeloablative chemotherapy followed by infusion of HLA-identical stem cells for relapsed leukaemia and lymphoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Fludarabine-based preparative protocol for unrelated donor cord blood transplantation in children: successful engraftment with minimal toxicity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703567

7 January 2021

Identifiers

DOI

10.1038/SJ.BMT.1703567

1 reference

Dimensions Publication ID

4 August 2017

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1 reference