(Q34251009)

English

X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings

scientific article

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scholarly article

1 reference

Europe PubMed Central

31 July 2017

X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings (English)

1 reference

Europe PubMed Central

31 July 2017

severe combined immunodeficiency

1 reference

based on heuristic

inferred from title

author name string

M E Conley

1

1 reference

Europe PubMed Central

31 July 2017

R H Buckley

2

1 reference

Europe PubMed Central

31 July 2017

R Hong

3

1 reference

Europe PubMed Central

31 July 2017

C Guerra-Hanson

4

1 reference

Europe PubMed Central

31 July 2017

C M Roifman

5

1 reference

Europe PubMed Central

31 July 2017

J A Brochstein

6

1 reference

Europe PubMed Central

31 July 2017

S Pahwa

7

1 reference

Europe PubMed Central

31 July 2017

J M Puck

8

1 reference

Europe PubMed Central

31 July 2017

language of work or name

0 references

publication date

1 May 1990

1 reference

Europe PubMed Central

31 July 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

31 July 2017

85

1 reference

Europe PubMed Central

31 July 2017

1548-1554

1 reference

Europe PubMed Central

31 July 2017

5

1 reference

Europe PubMed Central

31 July 2017

Genetic deficiencies of adenosine deaminase and purine nucleoside phosphorylase: overview, genetic heterogeneity and therapy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Diagnosis and classification of severe combined immunodeficiency disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Transplantation for severe combined immunodeficiency with HLA-A,B,D,DR incompatible parental marrow cells fractionated by soybean agglutinin and sheep red blood cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Immunologic reconstitution after haploidentical bone marrow transplantation for immune deficiency disorders: treatment of bone marrow cells with monoclonal antibody CT-2 and complement.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Adenosine deaminase and purine nucleoside phosphorylase deficiencies: evaluation of therapeutic interventions in eight patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Development of immunity in human severe primary T cell deficiency following haploidentical bone marrow stem cell transplantation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Report of the committee on the genetic constitution of the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

X-linked agammaglobulinemia: an analysis of 96 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Heterogeneity of lymphocyte subpopulations in severe combined immunodeficiency. Evidence against a stem cell defect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Selective defect of precursor T cells associated with apparently normal B lymphocytes in severe combined immunodeficiency disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296604

6 July 2018

Presence of plasma cells and gamma-1-M-globulin synthesis in a patient with thymic alymphoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2332505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transfer factor induced delayed hypersensitivity in X-linked combined immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2332505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

XX T cells and XY B cells in two patients with severe combined immune deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2332505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clonal analysis using recombinant DNA probes from the X-chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2332505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accelerated development of immunity following transplantation of maternal marrow stem cells into infants with severe combined immunodeficiency and transplacentally acquired lymphoid chimerism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2332505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thymic dysplasia ("Swiss agammaglobulinemia"). I. Graft versus host reaction following bone-marrow transfusion

1 reference

https://pubmed.ncbi.nlm.nih.gov/2332505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI114603

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

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0 references

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