(Q34388591)

1 August 2017

Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity (English)

1 reference

familial hemophagocytic lymphohistiocytosis

1 August 2017

0 references

1 reference

Dufourcq-Lagelouse R

1

1 reference

1 August 2017

Jabado N

2

1 reference

1 August 2017

Le Deist F

3

1 reference

1 August 2017

Stéphan JL

4

1 reference

1 August 2017

Souillet G

5

1 reference

1 August 2017

Bruin M

6

1 reference

1 August 2017

Vilmer E

7

1 reference

1 August 2017

Schneider M

8

1 reference

1 August 2017

Janka G

9

1 reference

1 August 2017

Fischer A

10

1 reference

1 August 2017

de Saint Basile G

11

1 reference

1 August 2017

language of work or name

English

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publication date

1 January 1999

1 reference

American Journal of Human Genetics

1 August 2017

1 reference

1 August 2017

64

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1 August 2017

172-179

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1 August 2017

1

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Familial haemophagocytic reticulosis

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Familial hemophagocytic lymphohistiocytosis. Primary hemophagocytic lymphohistiocytosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Identification of mutations in two major mRNA isoforms of the Chediak-Higashi syndrome gene in human and mouse

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Parametric and nonparametric linkage analysis: a unified multipoint approach

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte Society.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

A comprehensive genetic map of the human genome based on 5,264 microsatellites

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Malignant lymphoma and erythrophagocytosis simulating malignant histiocytosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Hypercytokinemia in familial hemophagocytic lymphohistiocytosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Dinucleotide repeat polymorphism at the human CTLA4 gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

A syndrome associating partial albinism and immunodeficiency

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Virus-associated hemophagocytic syndromeA benign histiocytic proliferation distinct from malignant histiocytosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

X-linked recessive progressive combined variable immunodeficiency (Duncan's disease)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Successful correction of hemophagocytic lymphohistiocytosis with related or unrelated bone marrow transplantation.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

Avoiding recomputation in linkage analysis.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377715

[The accelerated phase of Chediak-Higashi syndrome]

27 October 2018

1 reference

12 December 2020

Linkage analysis and family classification under heterogeneity

1 reference

12 December 2020

A polymorphic dinucleotide repeat in the human IL-10 promoter

1 reference

12 December 2020

Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping

1 reference

12 December 2020

Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A

1 reference

12 December 2020

Frequency and severity of central nervous system lesions in hemophagocytic lymphohistiocytosis

1 reference

12 December 2020

Treatment of familial hemophagocytic lymphohistiocytosis with bone marrow transplantation from HLA genetically nonidentical donors

1 reference

12 December 2020

Identifiers

DOI

10.1086/302194

1 reference

1 August 2017

1 reference

1 August 2017

1 reference