-
1
-
-
0036224043
-
Primary immunodeficiency disorders: antibody deficiency
-
Ballow M. Primary immunodeficiency disorders: antibody deficiency. J. Allergy Clin. Immunol. 109 (2002) 581-591
-
(2002)
J. Allergy Clin. Immunol.
, vol.109
, pp. 581-591
-
-
Ballow, M.1
-
2
-
-
0027538145
-
Primary hypogammaglobulinemia: a survey of clinical manifestations and complications
-
Hermaszewski R.A., and Webster A.D. Primary hypogammaglobulinemia: a survey of clinical manifestations and complications. Q. J. Med. 86 (1993) 31-42
-
(1993)
Q. J. Med.
, vol.86
, pp. 31-42
-
-
Hermaszewski, R.A.1
Webster, A.D.2
-
3
-
-
0032976666
-
Common variable immunodeficiency: clinical and immunological features of 248 patients
-
Cunningham-Rundles C., and Bodian C. Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin. Immunol. 92 (1992) 34-48
-
(1992)
Clin. Immunol.
, vol.92
, pp. 34-48
-
-
Cunningham-Rundles, C.1
Bodian, C.2
-
6
-
-
27944467842
-
TACItly changing tunes: farewell to a yin and yang of BAFF receptor and TACI in humoral immunity? New genetic defects in common variable immunodeficiency
-
Salzer U., and Grimbacher B. TACItly changing tunes: farewell to a yin and yang of BAFF receptor and TACI in humoral immunity? New genetic defects in common variable immunodeficiency. Curr. Opin. Allergy Clin. Immunol. 5 (2005) 496-503
-
(2005)
Curr. Opin. Allergy Clin. Immunol.
, vol.5
, pp. 496-503
-
-
Salzer, U.1
Grimbacher, B.2
-
7
-
-
0034041626
-
Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry
-
Kanegane H., Tsukada S., Iwata T., et al. Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry. Clin. Exp. Immunol. 120 (2000) 512-517
-
(2000)
Clin. Exp. Immunol.
, vol.120
, pp. 512-517
-
-
Kanegane, H.1
Tsukada, S.2
Iwata, T.3
-
8
-
-
10344239867
-
Mutations in the mu heavy-chain gene in patients with agammaglobulinaemia
-
Yel L., Minegishi Y., Coustan-Smith E., et al. Mutations in the mu heavy-chain gene in patients with agammaglobulinaemia. N. Engl. J. Med. 335 (1996) 1486-1493
-
(1996)
N. Engl. J. Med.
, vol.335
, pp. 1486-1493
-
-
Yel, L.1
Minegishi, Y.2
Coustan-Smith, E.3
-
9
-
-
0031594211
-
Mutations in the human lambda 5/14.1 gene result in B cell deficiency and agammaglobulinaemia
-
Minegishi Y., Coustan-Smith E., Wang Y.H., Cooper M.D., Campana D., and Conley M.E. Mutations in the human lambda 5/14.1 gene result in B cell deficiency and agammaglobulinaemia. J. Exp. Med. 187 (1998) 71-77
-
(1998)
J. Exp. Med.
, vol.187
, pp. 71-77
-
-
Minegishi, Y.1
Coustan-Smith, E.2
Wang, Y.H.3
Cooper, M.D.4
Campana, D.5
Conley, M.E.6
-
10
-
-
0033521148
-
An essential role for BLNK in human B cell development
-
Minegishi Y., Rohrer J., Coustan-Smith E., et al. An essential role for BLNK in human B cell development. Science 286 (1999) 1954-1957
-
(1999)
Science
, vol.286
, pp. 1954-1957
-
-
Minegishi, Y.1
Rohrer, J.2
Coustan-Smith, E.3
-
11
-
-
13144253109
-
Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical molecular, and immunological features
-
Lougaris V., Badolato R., Ferrari S., and Plebani A. Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical molecular, and immunological features. Immunol. Rev. 203 (2005) 48-66
-
(2005)
Immunol. Rev.
, vol.203
, pp. 48-66
-
-
Lougaris, V.1
Badolato, R.2
Ferrari, S.3
Plebani, A.4
-
12
-
-
0034264851
-
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)
-
Revy P., Muto T., Levy Y., et al. Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). Cell 102 (2000) 565-575
-
(2000)
Cell
, vol.102
, pp. 565-575
-
-
Revy, P.1
Muto, T.2
Levy, Y.3
-
13
-
-
0142092610
-
Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination
-
Imai K., Slupphaug G., Lee W.I., et al. Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination. Nat. Immunol. 4 (2003) 1023-1028
-
(2003)
Nat. Immunol.
, vol.4
, pp. 1023-1028
-
-
Imai, K.1
Slupphaug, G.2
Lee, W.I.3
-
14
-
-
1642401844
-
Defective B-cell-negative selection and terminal differentiation in the ICF syndrome
-
Blanco-Betancourt C.E., Moncla A., Milili M., et al. Defective B-cell-negative selection and terminal differentiation in the ICF syndrome. Blood 103 (2004) 2683-2690
-
(2004)
Blood
, vol.103
, pp. 2683-2690
-
-
Blanco-Betancourt, C.E.1
Moncla, A.2
Milili, M.3
-
15
-
-
23044463627
-
TACI is mutant in common variable immunodeficiency and IgA deficiency
-
Castigli E., Wilson S.A., Garibyan L., et al. TACI is mutant in common variable immunodeficiency and IgA deficiency. Nat. Genet. 37 (2005) 829-834
-
(2005)
Nat. Genet.
, vol.37
, pp. 829-834
-
-
Castigli, E.1
Wilson, S.A.2
Garibyan, L.3
-
16
-
-
23044443492
-
Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans
-
Salzer U., Chapel H.M., Webster A.D., et al. Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. Nat. Genet. 37 (2005) 820-828
-
(2005)
Nat. Genet.
, vol.37
, pp. 820-828
-
-
Salzer, U.1
Chapel, H.M.2
Webster, A.D.3
-
17
-
-
0027394391
-
The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome
-
Aruffo A., Farrington M., Hollenbaugh D., et al. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome. Cell 72 (1993) 291-300
-
(1993)
Cell
, vol.72
, pp. 291-300
-
-
Aruffo, A.1
Farrington, M.2
Hollenbaugh, D.3
-
18
-
-
0037340349
-
Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency
-
Grimbacher B., Hutloff A., Schlesier M., et al. Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency. Nat. Immunol. 4 (2003) 261-268
-
(2003)
Nat. Immunol.
, vol.4
, pp. 261-268
-
-
Grimbacher, B.1
Hutloff, A.2
Schlesier, M.3
-
19
-
-
0036260179
-
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome
-
Gennery A.R., Barge D., O'Sullivan J.J., Flood T.J., Abinun M., and Cant A.J. Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome. Arch. Dis. Child. 86 (2002) 422-425
-
(2002)
Arch. Dis. Child.
, vol.86
, pp. 422-425
-
-
Gennery, A.R.1
Barge, D.2
O'Sullivan, J.J.3
Flood, T.J.4
Abinun, M.5
Cant, A.J.6
-
20
-
-
4344609133
-
Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency
-
Eastwood D., Gilmour K.C., Nistala K., et al. Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency. Clin. Exp. Immunol. 137 (2004) 584-588
-
(2004)
Clin. Exp. Immunol.
, vol.137
, pp. 584-588
-
-
Eastwood, D.1
Gilmour, K.C.2
Nistala, K.3
-
21
-
-
33746846393
-
Redefining autoimmunity in primary immunodeficiency diseases
-
Arkwright P.D., Abinun M., and Cant A.J. Redefining autoimmunity in primary immunodeficiency diseases. Blood 100 (2002) 2678-2679
-
(2002)
Blood
, vol.100
, pp. 2678-2679
-
-
Arkwright, P.D.1
Abinun, M.2
Cant, A.J.3
-
22
-
-
4444379717
-
Primary immunodeficiency diseases: an update
-
Notarangelo L., Casanova J.L., Fischer A., Puck J., Rosen F., Seger R., and Geha R. Primary immunodeficiency diseases: an update. J. Allergy Clin. Immunol. 114 (2004) 677-687
-
(2004)
J. Allergy Clin. Immunol.
, vol.114
, pp. 677-687
-
-
Notarangelo, L.1
Casanova, J.L.2
Fischer, A.3
Puck, J.4
Rosen, F.5
Seger, R.6
Geha, R.7
-
23
-
-
0032879799
-
Report of an IUIS Scientific Committee
-
International Union of Immunological Societies. Primary immunodeficiency diseases. Report of an IUIS Scientific Committee. Clin. Exp. Immunol. 118 Suppl 1 (1999) 1-28
-
(1999)
Clin. Exp. Immunol.
, vol.118
, Issue.SUPPL. 1
, pp. 1-28
-
-
-
24
-
-
0032737534
-
Pulmonary abnormalities in patients with primary hypogammaglobulinemia
-
Kainulainen L., Varpula M., Liippo K., et al. Pulmonary abnormalities in patients with primary hypogammaglobulinemia. J. Allergy Clin. Immunol. 104 (1999) 1031-1036
-
(1999)
J. Allergy Clin. Immunol.
, vol.104
, pp. 1031-1036
-
-
Kainulainen, L.1
Varpula, M.2
Liippo, K.3
-
25
-
-
0025353943
-
Classification of patients with common variable immunodeficiency by B cell secretion of IgM and IgG in response to anti-IgM and interleukin-2
-
Bryant A., Calver N.C., Toubi E., Webster A.D., and Farrant J. Classification of patients with common variable immunodeficiency by B cell secretion of IgM and IgG in response to anti-IgM and interleukin-2. Clin. Immunol. Immunopathol. 56 (1990) 239-248
-
(1990)
Clin. Immunol. Immunopathol.
, vol.56
, pp. 239-248
-
-
Bryant, A.1
Calver, N.C.2
Toubi, E.3
Webster, A.D.4
Farrant, J.5
-
26
-
-
0042332029
-
Common variable immunodeficiency. Patient classification based on impaired B cell memory differentiation correlates with clinical aspects
-
Piqueras B., Lavenu-Bombled C., Galicier L., et al. Common variable immunodeficiency. Patient classification based on impaired B cell memory differentiation correlates with clinical aspects. J. Clin. Immunol. 5 (2003) 385-400
-
(2003)
J. Clin. Immunol.
, vol.5
, pp. 385-400
-
-
Piqueras, B.1
Lavenu-Bombled, C.2
Galicier, L.3
-
27
-
-
0036493366
-
-) in subgroups of patients with common variable immunodeficiency (CVID): a new approach to classify a heterogeneous disease
-
-) in subgroups of patients with common variable immunodeficiency (CVID): a new approach to classify a heterogeneous disease. Blood 99 (2002) 1544-1551
-
(2002)
Blood
, vol.99
, pp. 1544-1551
-
-
Warnatz, K.1
Denz, A.2
Drager, R.3
-
28
-
-
13444278991
-
The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency
-
Carsetti R., Rosado M.M., Donnanno S., et al. The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency. J. Allergy Clin. Immunol. 115 (2005) 412-417
-
(2005)
J. Allergy Clin. Immunol.
, vol.115
, pp. 412-417
-
-
Carsetti, R.1
Rosado, M.M.2
Donnanno, S.3
-
29
-
-
19544378527
-
Immune competence and switched memory B cells in common variable immunodeficiency
-
Ko J., Radigan L., and Cunningham-Rundles C. Immune competence and switched memory B cells in common variable immunodeficiency. Clin. Immunol. 116 (2005) 37-41
-
(2005)
Clin. Immunol.
, vol.116
, pp. 37-41
-
-
Ko, J.1
Radigan, L.2
Cunningham-Rundles, C.3
-
30
-
-
0027245077
-
The acquisition of anti-pneumococcal capsular polysaccharide Haemophilus influenzae type b and tetanus toxoid antibodies with age in the UK
-
Hazlewood M., Nusrat R., Kumararatne D.S., et al. The acquisition of anti-pneumococcal capsular polysaccharide Haemophilus influenzae type b and tetanus toxoid antibodies with age in the UK. Clin. Exp. Immunol. 93: (1993) 57-64
-
(1993)
Clin. Exp. Immunol.
, vol.93
, pp. 57-64
-
-
Hazlewood, M.1
Nusrat, R.2
Kumararatne, D.S.3
-
31
-
-
0041324979
-
Measurement and interpretation of pneumococcal IgG levels for clinical management
-
Balmer P., North J., Baxter D., et al. Measurement and interpretation of pneumococcal IgG levels for clinical management. Clin. Exp. Immunol. 133 (2003) 364-369
-
(2003)
Clin. Exp. Immunol.
, vol.133
, pp. 364-369
-
-
Balmer, P.1
North, J.2
Baxter, D.3
-
32
-
-
4944257670
-
The role of activation-induced cytidine deaminase in antibody diversification, immunodeficiency, and B-cell malignancies
-
Luo Z., Ronai D., and Scharff M.D. The role of activation-induced cytidine deaminase in antibody diversification, immunodeficiency, and B-cell malignancies. J. Allergy Clin. Immunol. 114 (2004) 726-735
-
(2004)
J. Allergy Clin. Immunol.
, vol.114
, pp. 726-735
-
-
Luo, Z.1
Ronai, D.2
Scharff, M.D.3
-
33
-
-
1142310694
-
Human models of inherited immunoglobulin class switch recombination and somatic hypermutation defects (hyper-IgM syndromes)
-
Durandy A., Revy P., and Fischer A. Human models of inherited immunoglobulin class switch recombination and somatic hypermutation defects (hyper-IgM syndromes). Adv. Immunol. 82 (2004) 295-330
-
(2004)
Adv. Immunol.
, vol.82
, pp. 295-330
-
-
Durandy, A.1
Revy, P.2
Fischer, A.3
-
34
-
-
4444297541
-
Class switch recombination in B lymphopoiesis: a potential pathway for B cell autoimmunity
-
Diamant E., and Melamed D. Class switch recombination in B lymphopoiesis: a potential pathway for B cell autoimmunity. Autoimmun. Rev. 3 (2004) 464-469
-
(2004)
Autoimmun. Rev.
, vol.3
, pp. 464-469
-
-
Diamant, E.1
Melamed, D.2
-
35
-
-
8344290474
-
Common variable immunodeficiency and the gastrointestinal tract
-
Kalha I., and Sellin J.H. Common variable immunodeficiency and the gastrointestinal tract. Curr. Gastroenterol. Rep. 6 (2004) 377-383
-
(2004)
Curr. Gastroenterol. Rep.
, vol.6
, pp. 377-383
-
-
Kalha, I.1
Sellin, J.H.2
-
36
-
-
0034954783
-
Immuno-bacterial homeostasis in the gut: new insights into an old enigma
-
Elson C.O., Cong Y., Iqbal N., and Weaver C.T. Immuno-bacterial homeostasis in the gut: new insights into an old enigma. Semin. Immunol. 13 (2001) 187-194
-
(2001)
Semin. Immunol.
, vol.13
, pp. 187-194
-
-
Elson, C.O.1
Cong, Y.2
Iqbal, N.3
Weaver, C.T.4
-
37
-
-
13244291394
-
Anti-inflammatory effects of macrolides-an underappreciated benefit in the treatment of community-acquired respiratory tract infections and chronic inflammatory pulmonary conditions?
-
Amsden G.W. Anti-inflammatory effects of macrolides-an underappreciated benefit in the treatment of community-acquired respiratory tract infections and chronic inflammatory pulmonary conditions?. J. Antimicrob. Chemother. 55 (2005) 10-21
-
(2005)
J. Antimicrob. Chemother.
, vol.55
, pp. 10-21
-
-
Amsden, G.W.1
|