(Q43747131)

English

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.

scientific article published in August 2001

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scholarly article

1 reference

Europe PubMed Central

26 November 2017

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. (English)

1 reference

Europe PubMed Central

26 November 2017

Griscelli syndrome

1 reference

based on heuristic

inferred from title

author name string

F Schuster

1

1 reference

Europe PubMed Central

26 November 2017

D K Stachel

2

1 reference

Europe PubMed Central

26 November 2017

I Schmid

3

1 reference

Europe PubMed Central

26 November 2017

F A Baumeister

4

1 reference

Europe PubMed Central

26 November 2017

U B Graubner

5

1 reference

Europe PubMed Central

26 November 2017

M Weiss

6

1 reference

Europe PubMed Central

26 November 2017

R J Haas

7

1 reference

Europe PubMed Central

26 November 2017

B H Belohradsky

8

1 reference

Europe PubMed Central

26 November 2017

language of work or name

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publication date

1 August 2001

1 reference

Europe PubMed Central

26 November 2017

Bone Marrow Transplantation

1 reference

Europe PubMed Central

26 November 2017

28

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Europe PubMed Central

26 November 2017

409-412

1 reference

Europe PubMed Central

26 November 2017

4

1 reference

Europe PubMed Central

26 November 2017

https://scigraph.springernature.com/pub.10.1038/sj.bmt.1703114

0 references

A syndrome associating partial albinism and immunodeficiency

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

Accelerated phase in partial albinism with immunodeficiency (Griscelli syndrome): genetics and stem cell transplantation in a 2-month-old girl

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

Lymphoproliferative syndrome in an infant after stem cell transplantation: successful therapy with T-lymphocytes and anti-CD20 monoclonal antibodies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

Myosin V colocalizes with melanosomes and subcortical actin bundles not associated with stress fibers in human epidermal melanocytes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

Brain myosin V is a synaptic vesicle-associated motor protein: evidence for a Ca2+-dependent interaction with the synaptobrevin-synaptophysin complex

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

21 January 2018

Partial albinism with immunodeficiency (Griscelli syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

7 January 2021

based on heuristic

inferred from DOI database lookup

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.1703114

7 January 2021

based on heuristic

inferred from DOI database lookup

A kindred with Griscelli disease: spectrum of neurological involvement

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

7 January 2021

based on heuristic

inferred from DOI database lookup

Allogeneic bone marrow transplantation for erythrophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

7 January 2021

based on heuristic

inferred from DOI database lookup

Bone-marrow transplantation for immunodeficiencies and osteopetrosis: European survey, 1968-1985

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BMT.1703114

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.BMT.1703114

1 reference

Europe PubMed Central

26 November 2017

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1 reference

Europe PubMed Central

26 November 2017

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