Autoimmune lymphoproliferative syndrome. A human disorder of abnormal lymphocyte survival

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Autoimmune lymphoproliferative syndrome. A human disorder of abnormal lymphocyte survival is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.1016/S0031-3955(05)70272-8
P698PubMed publication ID11130997

P2093author name stringStraus SE
Fleisher TA
Bleesing JJ
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Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosisQ30080034
An inherited disorder of lymphocyte apoptosis: the autoimmune lymphoproliferative syndromeQ33328425
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Chronic pseudomalignant immuneproliferation (Canale-Smith syndrome) (author's transl)Q33345710
Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunityQ33488225
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Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunityQ33497763
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The spectrum of apoptotic defects and clinical manifestations, including systemic lupus erythematosus, in humans with CD95 (Fas/APO-1) mutationsQ33747849
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Defective CD95/APO-1/Fas signal complex formation in the human autoimmune lymphoproliferative syndrome, type Ia.Q35132088
CD5 B cells in autoimmunityQ35321025
A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld diseaseQ35604700
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Spontaneous development of plasmacytoid tumors in mice with defective Fas-Fas ligand interactionsQ36400965
Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiencyQ38467986
Fas gene mutation in the progression of adult T cell leukemiaQ40962746
Lymphadenopathy in childrenQ45113420
The use of the anti-malaria drug Fansidar (pyrimethamine and sulphadoxine) in the treatment of a patient with autoimmune lymphoproliferative syndrome and Fas deficiencyQ47720590
Alterations of Fas (Apo-1/CD95) gene in non-small cell lung cancer.Q54089913
Interleukin-2 reverses the defect in activation-induced apoptosis in T cells from autoimmune lpr mice.Q54139209
Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndromeQ55670225
Phenotypical and Functional Characterization of Double-Negative (CD4-CD8-) alphabeta T-Cell Receptor Positive Cells from an Immunodeficient PatientQ56112112
Dyserythropoiesis associated with a Fas-deficient condition in childhoodQ57078479
Increased spontaneous in vitro apoptosis in double negative T cells of humans with a fas/apo-1 mutationQ57956205
Fas/Apo1 mutations and autoimmune lymphoproliferative syndrome in a patient with type 2 autoimmune hepatitisQ58435123
Chronic lymphadenopathy simulating malignant lymphomaQ59242110
Novel T-lymphocyte population in combined immunodeficiency with features of graft-versus-host diseaseQ69741242
Chronic lymphoproliferative disordersQ73196685
Somatic mutations of Fas (Apo-1/CD95) gene in cutaneous squamous cell carcinoma arising from a burn scarQ73322019
Novel Fas (CD95/APO-1) mutations in infants with a lymphoproliferative disorderQ74418696
Correction of autoimmune lymphoproliferative syndrome by bone marrow transplantationQ77169432
The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosisQ77577103
Defective apoptosis due to a point mutation in the death domain of CD95 associated with autoimmune lymphoproliferative syndrome, T-cell lymphoma, and Hodgkin's diseaseQ77787538
P433issue6
P921main subjectautoimmune lymphoproliferative syndromeQ1151300
P304page(s)1291-1310
P577publication date2000-12-01
P1433published inPediatric Clinics of North AmericaQ7159204
P1476titleAutoimmune lymphoproliferative syndrome. A human disorder of abnormal lymphocyte survival
P478volume47

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cites work (P2860)
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