X-linked lymphoproliferative disease: three atypical cases (Q77067621)

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2 December 2019

title

X-linked lymphoproliferative disease: three atypical cases (English)

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2 December 2019

author name string

K Nistala

1

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2 December 2019

K C Gilmour

2

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2 December 2019

T Cranston

3

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2 December 2019

E G Davies

4

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2 December 2019

D Goldblatt

5

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2 December 2019

H B Gaspar

6

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2 December 2019

A M Jones

7

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publication date

1 October 2001

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Clinical and Experimental Immunology

2 December 2019

published in

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volume

126

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2 December 2019

issue

1

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2 December 2019

page(s)

126-130

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Cutting edge: human 2B4, an activating NK cell receptor, recruits the protein tyrosine phosphatase SHP-2 and the adaptor signaling protein SAP

2 December 2019

cites work

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12 December 2020

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

1 reference

12 December 2020

Atypical X-linked agammaglobulinemia diagnosed in three adults

1 reference

12 December 2020

Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome

1 reference

12 December 2020

Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease.

1 reference

12 December 2020

SH2D1A mutation analysis for diagnosis of XLP in typical and atypical patients

1 reference

12 December 2020

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

1 reference

12 December 2020

Recurrent B-cell non-Hodgkin's lymphoma in two brothers with X-linked lymphoproliferative disease without evidence for Epstein-Barr virus infection

1 reference

12 December 2020

Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case families

1 reference

12 December 2020

Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry

1 reference

12 December 2020

Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expression

1 reference

12 December 2020

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

1 reference

12 December 2020

Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative disease

1 reference

12 December 2020

Evaluation of families wherein a single male manifests a phenotype of X-linked lymphoproliferative disease (XLP).

1 reference

12 December 2020

Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease

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12 December 2020

X-linked lymphoproliferative disease: twenty-five years after the discovery

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12 December 2020

Cure of X-linked lymphoproliferative disease (XLP) with allogeneic hematopoietic stem cell transplantation (HSCT): report from the XLP registry.

1 reference

12 December 2020

Clinical spectrum of X-linked hyper-IgM syndrome

1 reference

12 December 2020

Extreme variation in X-linked agammaglobulinemia phenotype in a three-generation family

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12 December 2020

1 reference

12 December 2020

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

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12 December 2020

Common variable immunodeficiency: clinical and immunological features of 248 patients.

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12 December 2020

10.1046/J.1365-2249.2001.01599.X

Identifiers

DOI

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2 December 2019

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