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1
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0028985611
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Primary immunodeficiency diseases
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Report of a WHO Scientific Group: Primary immunodeficiency diseases. Clin Exp Immunol 1995, 99(suppl 1):2-24. A comprehensive update on the classification and pathogenesis of the primary immunodeficiencies. Unfortunately, it is unreferenced.
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(1995)
Clin Exp Immunol
, vol.99
, Issue.1 SUPPL.
, pp. 2-24
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2
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0025690483
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Adenosine deaminase deficiency
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Hirschhorn R: Adenosine deaminase deficiency. Immunodeficiency Rev 1990,2:175-198.
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(1990)
Immunodeficiency Rev
, vol.2
, pp. 175-198
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Hirschhorn, R.1
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3
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0028136274
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Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency
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Shovlin CL, Simmonds HA, Fairbanks LD, Deacock SJ, Hughes JMB, Lechler RI, Webster AD, Sun X, Webb JC, Southar AK: Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency. J Immunol 1994, 153:2331-2339. The first report of ADA deficiency presenting in adulthood.
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(1994)
J Immunol
, vol.153
, pp. 2331-2339
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Shovlin, C.L.1
Simmonds, H.A.2
Fairbanks, L.D.3
Deacock, S.J.4
Hughes, J.M.B.5
Lechler, R.I.6
Webster, A.D.7
Sun, X.8
Webb, J.C.9
Southar, A.K.10
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4
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0024538472
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Clinical and immunologic analyses of 103 patients with common variable immunodeficiency
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Cunningham-Rundles C: Clinical and immunologic analyses of 103 patients with common variable immunodeficiency. J Clin Immunol 1989, 9:22-33.
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(1989)
J Clin Immunol
, vol.9
, pp. 22-33
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Cunningham-Rundles, C.1
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5
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0027602669
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NIH Conference: New insights into common variable immunodeficiency
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Sneller MC, Strober W, Eisenstein E, Jaffe JS, Cunningham-Rundles C: NIH Conference: new insights into common variable immunodeficiency. Ann Intern Med 1993, 118:720-730.
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(1993)
Ann Intern Med
, vol.118
, pp. 720-730
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Sneller, M.C.1
Strober, W.2
Eisenstein, E.3
Jaffe, J.S.4
Cunningham-Rundles, C.5
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6
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0028935638
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Reduced IL-2 expression upon antigen stimulation is accompanied by deficient IL-9 gene expression in T cells of patients with CVID
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Hauber I, Fischer MB, Maris M, Eibl MM: Reduced IL-2 expression upon antigen stimulation is accompanied by deficient IL-9 gene expression in T cells of patients with CVID. Scand J Immunol 1995, 41:215-219. The authors explore a mechanism for the defective T cell activation in some patients with CVID.
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(1995)
Scand J Immunol
, vol.41
, pp. 215-219
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Hauber, I.1
Fischer, M.B.2
Maris, M.3
Eibl, M.M.4
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7
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0028003720
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A defect in the early phase of T cell receptor-mediated T cell activation in patients with common variable immunodeficiency
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Fischer MB, Hauber I, Eggenbauer H, Thon V, Vogel E, Schaffer E, Lokaj J, Litzman J, Wolf HM, Mannhalter JW, Eibl MM: A defect In the early phase of T cell receptor-mediated T cell activation in patients with common variable immunodeficiency. Blood 1994, 84:4234-4241. This study shows that a defect in the early phase of T cell activation is present in some patients with CVID.
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(1994)
Blood
, vol.84
, pp. 4234-4241
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Fischer, M.B.1
Hauber, I.2
Eggenbauer, H.3
Thon, V.4
Vogel, E.5
Schaffer, E.6
Lokaj, J.7
Litzman, J.8
Wolf, H.M.9
Mannhalter, J.W.10
Eibl, M.M.11
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8
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0028088276
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Immunodeficiency due to a faulty interaction between T cells and B cells
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Laman J, Claasen E, Noelle RJ: Immunodeficiency due to a faulty interaction between T cells and B cells. Curr Opin Immunol 1994, 6:636-641. Useful review highlighting the importance of defects in the interactions between T and B cells in the pathogenesis of immunodeficiency.
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(1994)
Curr Opin Immunol
, vol.6
, pp. 636-641
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Laman, J.1
Claasen, E.2
Noelle, R.J.3
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9
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0028323311
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Study of B and T cell phenotypes in blood from patients with common variable immunodeficiency (CVID)
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Farrant J, Spickett G, Matamoros N, Copas D, Hernandez M, North M, Chapel H, Webster AD: Study of B and T cell phenotypes in blood from patients with common variable immunodeficiency (CVID). Immunodeficiency 1994, 5:159-169. The authors demonstrate the importance of T cell regulation of B cell responses.
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(1994)
Immunodeficiency
, vol.5
, pp. 159-169
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Farrant, J.1
Spickett, G.2
Matamoros, N.3
Copas, D.4
Hernandez, M.5
North, M.6
Chapel, H.7
Webster, A.D.8
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10
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0028011077
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CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency
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Farrington M, Grosmaire LS, Nonoyama S, Fischer SH, Hollenbaugh D, Ledbetter JA, Noelle RJ, Aruffo A, Ochs HD: CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency. Proc Natl Acad Sci USA 1994, 91:1099-1103.
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(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 1099-1103
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Farrington, M.1
Grosmaire, L.S.2
Nonoyama, S.3
Fischer, S.H.4
Hollenbaugh, D.5
Ledbetter, J.A.6
Noelle, R.J.7
Aruffo, A.8
Ochs, H.D.9
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11
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0028201730
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The CD40 antigen and its ligand
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Banchereau J, Bazan F, Blanchard D, Briere F, Galizzi JP, van Kooten C, Liu YJ, Roussel F, Saeland S: The CD40 antigen and its ligand. Annu Rev Immunol 1994, 12:881-922.
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(1994)
Annu Rev Immunol
, vol.12
, pp. 881-922
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Banchereau, J.1
Bazan, F.2
Blanchard, D.3
Briere, F.4
Galizzi, J.P.5
Van Kooten, C.6
Liu, Y.J.7
Roussel, F.8
Saeland, S.9
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12
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0028146992
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Hyper IgM syndrome associated with defective CD40 mediated B cell activation
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Conley ME, Larche M, Bonagura VR, Lawton AR, Buckley RH, Fu SM, Coustan-Smith E, Herrod HG, Campana D: Hyper IgM syndrome associated with defective CD40 mediated B cell activation. J Clin Invest 1994, 94:1404-1409. This report shows that in a subset of patients with hyper IgM syndrome, in addition to the defective expression of CD40 ligand, defective signal transduction occurs in T cells expressing CD40 ligand.
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(1994)
J Clin Invest
, vol.94
, pp. 1404-1409
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Conley, M.E.1
Larche, M.2
Bonagura, V.R.3
Lawton, A.R.4
Buckley, R.H.5
Fu, S.M.6
Coustan-Smith, E.7
Herrod, H.G.8
Campana, D.9
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13
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0027937345
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Hyper IgM syndrome: Two mutations distinguish HIM
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Foy TM, Masters SR, Noelle RJ: Hyper IgM syndrome: two mutations distinguish HIM. J Clin Invest 1994, 94:1349-1350. This editorial discusses the work of Conley et al. (J Clin Invest 1994, 94:1404-1409) from the perspective of other recent findings and draws attention to the potential importance of the unique nonredundancy of the CD40-CD40 ligand interaction in T cell-dependent humoral immunity.
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(1994)
J Clin Invest
, vol.94
, pp. 1349-1350
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Foy, T.M.1
Masters, S.R.2
Noelle, R.J.3
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14
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0029074506
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Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene
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Kwan SP, Hagemann TL, Radtke BE, Blaese RM, Rosen FS: Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene. Proc Natl Acad Sci U S A 1995, 92:4706-4710. Further characterization of the molecular basis of the Wiskott-Aldrich syndrome.
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(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 4706-4710
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Kwan, S.P.1
Hagemann, T.L.2
Radtke, B.E.3
Blaese, R.M.4
Rosen, F.S.5
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15
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0028183399
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The genetic basis of chronic granulomatous disease
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Roos D: The genetic basis of chronic granulomatous disease. Immunol Rev 1994, 138:121-157. A useful review of the molecular biology and clinical aspects of chronic granulomatous disease.
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(1994)
Immunol Rev
, vol.138
, pp. 121-157
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Roos, D.1
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16
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0028913564
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A variant X-linked chronic granulomatous disease patient (X91+) with partially functional cytochrome b
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Cross AR, Heywoth PG, Rae J, Curnutte JT: A variant X-linked chronic granulomatous disease patient (X91+) with partially functional cytochrome b. J Biol Chem 1995, 270:8194-8200. The authors illustrate the heterogeneity of the mutations accounting for CGD.
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(1995)
J Biol Chem
, vol.270
, pp. 8194-8200
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Cross, A.R.1
Heywoth, P.G.2
Rae, J.3
Curnutte, J.T.4
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17
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0028893203
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Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte Superoxide production
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Pollock JD, Williams DA, Gifford MA, Li LL, Du X, Fisherman J, Orkin SH, Doerschuk CM, Dinauer MC: Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte Superoxide production. Nat Genet 1995, 9:202-209. The authors describe a mouse model of CGD that will be useful for study of this condition.
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(1995)
Nat Genet
, vol.9
, pp. 202-209
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Pollock, J.D.1
Williams, D.A.2
Gifford, M.A.3
Li, L.L.4
Du, X.5
Fisherman, J.6
Orkin, S.H.7
Doerschuk, C.M.8
Dinauer, M.C.9
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19
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0028315882
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Polyarthritis resembling juvenile rheumatoid arthritis in a girl with chronic granulomatous disease
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Lee BW, Yap H: Polyarthritis resembling juvenile rheumatoid arthritis in a girl with chronic granulomatous disease. Arthritis Rheum 1994, 37:773-776. An unusual case, providing a reminder that the association with autoimmune disease is not restricted to the immunodeficiencies associated with decreased immunoglobulins.
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(1994)
Arthritis Rheum
, vol.37
, pp. 773-776
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Lee, B.W.1
Yap, H.2
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20
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0028812516
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Cancer in children with primary or secondary immunodeficiencies
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Mueller BU, Pizzo PA: Cancer in children with primary or secondary immunodeficiencies. J Pediatr 1995, 126:1-10. A useful review of the frequency and types of malignancies occurring in immunodeficient patients, particularly children.
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(1995)
J Pediatr
, vol.126
, pp. 1-10
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Mueller, B.U.1
Pizzo, P.A.2
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21
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0028265349
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Lymphoproliferative disorders and other tumors complicating immunodeficiencies
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Filipovich AH, Mathur A, Kamat D, Kersey JH, Shapiro RS: Lymphoproliferative disorders and other tumors complicating immunodeficiencies. Immunodeficiency 1994, 5:91-112. A second review of malignancy complicating immunodeficiencies that reports the data from the Immunodeficiency Cancer Registry. Particularly good in discussing the role of Epstein-Barr virus.
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(1994)
Immunodeficiency
, vol.5
, pp. 91-112
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Filipovich, A.H.1
Mathur, A.2
Kamat, D.3
Kersey, J.H.4
Shapiro, R.S.5
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22
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84900356858
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Case records of the Massachusetts General Hospital: Case 7-1995
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Scully RE, Mark EM, McNeely WF, McNeely BU: Case records of the Massachusetts General Hospital: Case 7-1995. N Engl J Med 1995, 332:663-671. This case illustrates the diagnostic difficulties that face clinicians in dealing with immunodeficient patients in whom autoimmune disease, infection, and malignancy may be potential causes of illness.
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(1995)
N Engl J Med
, vol.332
, pp. 663-671
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Scully, R.E.1
Mark, E.M.2
McNeely, W.F.3
McNeely, B.U.4
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23
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0028017422
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Intravenous Immune globulin in primary immunodeficiency
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Haeney M: Intravenous Immune globulin in primary immunodeficiency. Clin Exp Immunol 1994, 97(suppl 1):11-15. The author reviews practical aspects of immunoglobulin therapy in immunodeficient patients.
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(1994)
Clin Exp Immunol
, vol.97
, Issue.1 SUPPL.
, pp. 11-15
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Haeney, M.1
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24
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0028857579
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Subcutaneous Immunoglobulin replacement in patients with primary antibody deficiencies: Safety and costs
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Gardulf A, Andersen V, Bjorkander J, Ericson D, Froland SS, Gustafson R, Hammarstrom L, Jacobsen MB, Jonsson E, Moller G, et al.: Subcutaneous Immunoglobulin replacement in patients with primary antibody deficiencies: safety and costs. Lancet 1995, 345:365-369. A report on the efficacy, safety, and cost of home-based subcutaneous immunoglobulin infusions.
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(1995)
Lancet
, vol.345
, pp. 365-369
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Gardulf, A.1
Andersen, V.2
Bjorkander, J.3
Ericson, D.4
Froland, S.S.5
Gustafson, R.6
Hammarstrom, L.7
Jacobsen, M.B.8
Jonsson, E.9
Moller, G.10
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25
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0028907019
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PEG-ADA: An alternative to haploidentical bone marrow transplantation and an adjunct to gene therapy for adenosine deaminase deficiency
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Hershfield MS. PEG-ADA: an alternative to haploidentical bone marrow transplantation and an adjunct to gene therapy for adenosine deaminase deficiency. Hum Mutat 1995, 5:107-112. A review of polyethylene glycol ADA in the management of SCID due to ADA deficiency.
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(1995)
Hum Mutat
, vol.5
, pp. 107-112
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Hershfield, M.S.1
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26
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0028024183
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Enhanced humoral immunity in common variable Immunodeficiency after long-term treatment with polyethylene glycol-conjugated lnterleukin-2
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Cunningham-Rundles C, Kazbay K, Hassett J, Zhou Z, Mayer L: Enhanced humoral immunity in common variable Immunodeficiency after long-term treatment with polyethylene glycol-conjugated lnterleukin-2. N Engl J Med 1994, 331:918-922. A report of enhanced humoral immunity following treatment of CVID with polyethylene glycol-conjugated interleukin-2.
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(1994)
N Engl J Med
, vol.331
, pp. 918-922
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Cunningham-Rundles, C.1
Kazbay, K.2
Hassett, J.3
Zhou, Z.4
Mayer, L.5
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