-
2
-
-
3242697783
-
Autoimmune thrombocytopenic purpura and common variable immunodeficiency: Analysis of 21 cases and review of the literature
-
Michel M, Chanet V, Galicier L, et al. Autoimmune thrombocytopenic purpura and common variable immunodeficiency: analysis of 21 cases and review of the literature. Medicine (Baltimore) 2004; 83:254-263.
-
(2004)
Medicine (Baltimore)
, vol.83
, pp. 254-263
-
-
Michel, M.1
Chanet, V.2
Galicier, L.3
-
3
-
-
22444432594
-
Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID)
-
Wang J, Cunningham-Rundles C. Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID). J Autoimmun 2005; 25:57-62.
-
(2005)
J Autoimmun
, vol.25
, pp. 57-62
-
-
Wang, J.1
Cunningham-Rundles, C.2
-
4
-
-
0036787850
-
Autoimmunity in severe combined immunodeficiency (SCID)
-
author reply 2678-2679
-
Elhasid R, Bergman R, Etzioni A. Autoimmunity in severe combined immunodeficiency (SCID). Blood 2002; 100:2677-2678; author reply 2678-2679.
-
(2002)
Blood
, vol.100
, pp. 2677-2678
-
-
Elhasid, R.1
Bergman, R.2
Etzioni, A.3
-
5
-
-
44449162969
-
Autoimmunity in severe combined immunodeficiency (SCID): Lessons from patients and experimental models
-
Milner JD, Fasth A, Etzioni A. Autoimmunity in severe combined immunodeficiency (SCID): lessons from patients and experimental models. J Clin Immunol 2008; 28 (Suppl 1):S29-S33.
-
(2008)
J Clin Immunol
, vol.28
, Issue.SUPPL. 1
-
-
Milner, J.D.1
Fasth, A.2
Etzioni, A.3
-
8
-
-
33750826824
-
Intractable colitis associated with chronic granulomatous disease
-
Arimura Y, Goto A, Yamashita K, et al. Intractable colitis associated with chronic granulomatous disease. J Med Microbiol 2006; 55:1587- 1590.
-
(2006)
J Med Microbiol
, vol.55
, pp. 1587-1590
-
-
Arimura, Y.1
Goto, A.2
Yamashita, K.3
-
9
-
-
33747599652
-
Omenn syndrome: A lack of tolerance on the background of deficient lymphocyte development and maturation
-
Honig M, Schwarz K. Omenn syndrome: a lack of tolerance on the background of deficient lymphocyte development and maturation. Curr Opin Rheumatol 2006; 18:383-388.
-
(2006)
Curr Opin Rheumatol
, vol.18
, pp. 383-388
-
-
Honig, M.1
Schwarz, K.2
-
10
-
-
0034698825
-
Homeostatic T cell proliferation: How far can T cells be activated to self-ligands?
-
Surh CD, Sprent J. Homeostatic T cell proliferation: how far can T cells be activated to self-ligands? J Exp Med 2000; 192:F9-F14.
-
(2000)
J Exp Med
, vol.192
-
-
Surh, C.D.1
Sprent, J.2
-
11
-
-
0037114168
-
Naive B lymphocytes undergo homeostatic proliferation in response to B cell deficit
-
Cabatingan MS, Schmidt MR, Sen R, Woodland RT. Naive B lymphocytes undergo homeostatic proliferation in response to B cell deficit. J Immunol 2002; 169:6795-6805.
-
(2002)
J Immunol
, vol.169
, pp. 6795-6805
-
-
Cabatingan, M.S.1
Schmidt, M.R.2
Sen, R.3
Woodland, R.T.4
-
12
-
-
0037243278
-
Neonates support lymphopeniainduced proliferation
-
Min B, McHugh R, Sempowski GD, et al. Neonates support lymphopeniainduced proliferation. Immunity 2003; 18:131-140.
-
(2003)
Immunity
, vol.18
, pp. 131-140
-
-
Min, B.1
McHugh, R.2
Sempowski, G.D.3
-
13
-
-
0037124362
-
Cytokine requirements for acute and basal homeostatic proliferation of naive and memory CD8+ T cells
-
Goldrath AW, Sivakumar PV, Glaccum M, et al. Cytokine requirements for acute and basal homeostatic proliferation of naive and memory CD8+ T cells. J Exp Med 2002; 195:1515-1522.
-
(2002)
J Exp Med
, vol.195
, pp. 1515-1522
-
-
Goldrath, A.W.1
Sivakumar, P.V.2
Glaccum, M.3
-
14
-
-
11144221749
-
The new paradigm of T-cell homeostatic proliferation-induced autoimmunity
-
Baccala R, Theofilopoulos AN. The new paradigm of T-cell homeostatic proliferation-induced autoimmunity. Trends Immunol 2005; 26:5-8.
-
(2005)
Trends Immunol
, vol.26
, pp. 5-8
-
-
Baccala, R.1
Theofilopoulos, A.N.2
-
15
-
-
1942453326
-
Homeostatic expansion of T cells during immune insufficiency generates autoimmunity
-
King C, Ilic A, Koelsch K, Sarvetnick N. Homeostatic expansion of T cells during immune insufficiency generates autoimmunity. Cell 2004; 117:265- 277.
-
(2004)
Cell
, vol.117
, pp. 265-277
-
-
King, C.1
Ilic, A.2
Koelsch, K.3
Sarvetnick, N.4
-
16
-
-
34248176213
-
Homeostatically proliferating CD4 T cells are involved in the pathogenesis of an Omenn syndrome murine model
-
Another link between lymphopenia and homeostatic expansion of T cells in a mouse model of Omenn syndrome
-
Khiong K, Murakami M, Kitabayashi C, et al. Homeostatically proliferating CD4 T cells are involved in the pathogenesis of an Omenn syndrome murine model. J Clin Invest 2007; 117:1270-1281. Another link between lymphopenia and homeostatic expansion of T cells in a mouse model of Omenn syndrome.
-
(2007)
J Clin Invest
, vol.117
, pp. 1270-1281
-
-
Khiong, K.1
Murakami, M.2
Kitabayashi, C.3
-
17
-
-
34248229621
-
A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome
-
Marrella V, Poliani PL, Casati A, et al. A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome. J Clin Invest 2007; 117:1260-1269.
-
(2007)
J Clin Invest
, vol.117
, pp. 1260-1269
-
-
Marrella, V.1
Poliani, P.L.2
Casati, A.3
-
18
-
-
0025295238
-
Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients
-
Ahonen P, Myllarniemi S, Sipila I, Perheentupa J. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. N Engl J Med 1990; 322:1829-1836.
-
(1990)
N Engl J Med
, vol.322
, pp. 1829-1836
-
-
Ahonen, P.1
Myllarniemi, S.2
Sipila, I.3
Perheentupa, J.4
-
19
-
-
0037383758
-
Aire regulates negative selection of organspecific T cells
-
Liston A, Lesage S, Wilson J, et al. Aire regulates negative selection of organspecific T cells. Nat Immunol 2003; 4:350-354.
-
(2003)
Nat Immunol
, vol.4
, pp. 350-354
-
-
Liston, A.1
Lesage, S.2
Wilson, J.3
-
20
-
-
0037084784
-
Aire deficient mice develop multiple features of APECED phenotype and show altered immune response
-
Ramsey C, Winqvist O, Puhakka L, et al. Aire deficient mice develop multiple features of APECED phenotype and show altered immune response. Hum Mol Genet 2002; 11:397-409.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 397-409
-
-
Ramsey, C.1
Winqvist, O.2
Puhakka, L.3
-
21
-
-
0037112047
-
Projection of an immunological self shadow within the thymus by the aire protein
-
Anderson MS, Venanzi ES, Klein L, et al. Projection of an immunological self shadow within the thymus by the aire protein. Science 2002; 298:1395- 1401.
-
(2002)
Science
, vol.298
, pp. 1395-1401
-
-
Anderson, M.S.1
Venanzi, E.S.2
Klein, L.3
-
22
-
-
20044376279
-
AIRE deficiency in thymus of 2 patients with Omenn syndrome
-
Cavadini P, Vermi W, Facchetti F, et al. AIRE deficiency in thymus of 2 patients with Omenn syndrome. J Clin Invest 2005; 115:728-732.
-
(2005)
J Clin Invest
, vol.115
, pp. 728-732
-
-
Cavadini, P.1
Vermi, W.2
Facchetti, F.3
-
24
-
-
0038434099
-
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis
-
Gambineri E, Torgerson TR, Ochs HD. Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis. Curr Opin Rheumatol 2003; 15:430-435.
-
(2003)
Curr Opin Rheumatol
, vol.15
, pp. 430-435
-
-
Gambineri, E.1
Torgerson, T.R.2
Ochs, H.D.3
-
25
-
-
0036346861
-
Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome
-
Wildin RS, Smyk-Pearson S, Filipovich AH. Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome. J Med Genet 2002; 39:537-545.
-
(2002)
J Med Genet
, vol.39
, pp. 537-545
-
-
Wildin, R.S.1
Smyk-Pearson, S.2
Filipovich, A.H.3
-
26
-
-
53149085302
-
Homeostatic proliferation in the mice with germline • FoxP3 mutation and its contribution to fatal autoimmunity
-
An interesting paper implicating homeostatic proliferation in the genesis of autoimmunity in FoxP3 mutant mice
-
Chang X, Zheng P, Liu Y. Homeostatic proliferation in the mice with germline • FoxP3 mutation and its contribution to fatal autoimmunity. J Immunol 2008; 181:2399-2406. An interesting paper implicating homeostatic proliferation in the genesis of autoimmunity in FoxP3 mutant mice.
-
(2008)
J Immunol
, vol.181
, pp. 2399-2406
-
-
Chang, X.1
Zheng, P.2
Liu, Y.3
-
28
-
-
0021914994
-
Subset specificity of antilymphocyte antibodies in systemic lupus erythematosus: Preferential reactivity with cells bearing the T4 and autologous erythrocyte receptor phenotypes
-
Yamada A, Cohen PL, Winfield JB. Subset specificity of antilymphocyte antibodies in systemic lupus erythematosus: preferential reactivity with cells bearing the T4 and autologous erythrocyte receptor phenotypes. Arthritis Rheum 1985; 28:262-270.
-
(1985)
Arthritis Rheum
, vol.28
, pp. 262-270
-
-
Yamada, A.1
Cohen, P.L.2
Winfield, J.B.3
-
29
-
-
0021366339
-
Relationship between systemic lupus erythematosus T cell subsets, anti-T cell antibodies, and T cell functions
-
Morimoto C, Reinherz EL, Distaso JA, et al. Relationship between systemic lupus erythematosus T cell subsets, anti-T cell antibodies, and T cell functions. J Clin Invest 1984; 73:689-700.
-
(1984)
J Clin Invest
, vol.73
, pp. 689-700
-
-
Morimoto, C.1
Reinherz, E.L.2
Distaso, J.A.3
-
30
-
-
0030702854
-
Clinical spectrum of X-linked hyper- IgM syndrome
-
Levy J, Espanol-Boren T, Thomas C, et al. Clinical spectrum of X-linked hyper- IgM syndrome. J Pediatr 1997; 131:47-54.
-
(1997)
J Pediatr
, vol.131
, pp. 47-54
-
-
Levy, J.1
Espanol-Boren, T.2
Thomas, C.3
-
31
-
-
0345276650
-
The X-linked hyper-IgM syndrome: Clinical and immunologic features of 79 patients
-
Winkelstein JA, Marino MC, Ochs H, et al. The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients. Medicine (Baltimore) 2003; 82:373-384.
-
(2003)
Medicine (Baltimore)
, vol.82
, pp. 373-384
-
-
Winkelstein, J.A.1
Marino, M.C.2
Ochs, H.3
-
32
-
-
47149093903
-
-
Arceci RJ. When T cells and macrophages do not talk: the hemophagocytic syndromes. Curr Opin Hematol 2008; 15:359-367.
-
Arceci RJ. When T cells and macrophages do not talk: the hemophagocytic syndromes. Curr Opin Hematol 2008; 15:359-367.
-
-
-
-
33
-
-
13144302865
-
Molecular and cellular pathogenesis of X-linked lymphoproliferative disease
-
Nichols KE, Ma CS, Cannons JL, et al. Molecular and cellular pathogenesis of X-linked lymphoproliferative disease. Immunol Rev 2005; 203:180-199.
-
(2005)
Immunol Rev
, vol.203
, pp. 180-199
-
-
Nichols, K.E.1
Ma, C.S.2
Cannons, J.L.3
-
34
-
-
17344372694
-
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2- domain encoding gene
-
Coffey AJ, Brooksbank RA, Brandau O, et al. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2- domain encoding gene. Nat Genet 1998; 20:129-135.
-
(1998)
Nat Genet
, vol.20
, pp. 129-135
-
-
Coffey, A.J.1
Brooksbank, R.A.2
Brandau, O.3
-
35
-
-
23044463627
-
TACI is mutant in common variable immunodeficiency and IgA deficiency
-
Castigli E, Wilson SA, Garibyan L, et al. TACI is mutant in common variable immunodeficiency and IgA deficiency. Nat Genet 2005; 37:829- 834.
-
(2005)
Nat Genet
, vol.37
, pp. 829-834
-
-
Castigli, E.1
Wilson, S.A.2
Garibyan, L.3
-
36
-
-
23044443492
-
Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans
-
Salzer U, Chapel HM, Webster AD, et al. Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. Nat Genet 2005; 37:820-828.
-
(2005)
Nat Genet
, vol.37
, pp. 820-828
-
-
Salzer, U.1
Chapel, H.M.2
Webster, A.D.3
-
37
-
-
0032976666
-
Common variable immunodeficiency: Clinical and immunological features of 248 patients
-
Cunningham-Rundles C, Bodian C. Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol 1999; 92:34-48.
-
(1999)
Clin Immunol
, vol.92
, pp. 34-48
-
-
Cunningham-Rundles, C.1
Bodian, C.2
-
38
-
-
0031857626
-
Juvenile rheumatoid arthritis and common variable hypogammaglobulinemia
-
Uluhan A, Sager D, Jasin HE. Juvenile rheumatoid arthritis and common variable hypogammaglobulinemia. J Rheumatol 1998; 25:1205-1210.
-
(1998)
J Rheumatol
, vol.25
, pp. 1205-1210
-
-
Uluhan, A.1
Sager, D.2
Jasin, H.E.3
-
39
-
-
12344297875
-
TACI and BAFF-R mediate isotype switching in B cells
-
Castigli E, Wilson SA, Scott S, et al. TACI and BAFF-R mediate isotype switching in B cells. J Exp Med 2005; 201:35-39.
-
(2005)
J Exp Med
, vol.201
, pp. 35-39
-
-
Castigli, E.1
Wilson, S.A.2
Scott, S.3
-
40
-
-
0034919939
-
Activation and accumulation of B cells in TACI- deficient mice
-
Yan M, Wang H, Chan B, et al. Activation and accumulation of B cells in TACI- deficient mice. Nat Immunol 2001; 2:638-643.
-
(2001)
Nat Immunol
, vol.2
, pp. 638-643
-
-
Yan, M.1
Wang, H.2
Chan, B.3
-
42
-
-
0037736679
-
Autoimmunity in Wiskott-Aldrich syndrome: Risk factors, clinical features, and outcome in a single-center cohort of 55 patients
-
Dupuis-Girod S, Medioni J, Haddad E, et al. Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients. Pediatrics 2003; 111 :e622-e627.
-
(2003)
Pediatrics
, vol.111
-
-
Dupuis-Girod, S.1
Medioni, J.2
Haddad, E.3
-
43
-
-
0033230229
-
Antigen receptor-induced activation and cytoskeletal rearrangement are impaired in Wiskott-Aldrich syndrome protein-deficient lymphocytes
-
Zhang J, Shehabeldin A, da Cruz LA, et al. Antigen receptor-induced activation and cytoskeletal rearrangement are impaired in Wiskott-Aldrich syndrome protein-deficient lymphocytes. J Exp Med 1999; 190:1329-1342.
-
(1999)
J Exp Med
, vol.190
, pp. 1329-1342
-
-
Zhang, J.1
Shehabeldin, A.2
da Cruz, L.A.3
-
44
-
-
20044375773
-
WASP deficiency leads to global defects of directed leukocyte migration in vitro and in vivo
-
Snapper SB, Meelu P, Nguyen D, et al. WASP deficiency leads to global defects of directed leukocyte migration in vitro and in vivo. J Leukoc Biol 2005; 77:993-998.
-
(2005)
J Leukoc Biol
, vol.77
, pp. 993-998
-
-
Snapper, S.B.1
Meelu, P.2
Nguyen, D.3
-
45
-
-
0037143734
-
Wiskott-Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cellactivating immunologic synapses
-
Orange JS, Ramesh N, Remold-O'Donnell E, et al. Wiskott-Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cellactivating immunologic synapses. Proc Natl Acad Sci U S A 2002; 99:11351-11356.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 11351-11356
-
-
Orange, J.S.1
Ramesh, N.2
Remold-O'Donnell, E.3
-
46
-
-
0347407821
-
Impaired signaling via the highaffinity IgE receptor in Wiskott-Aldrich syndrome protein-deficient mast cells
-
Pivniouk VI, Snapper SB, Kettner A, et al. Impaired signaling via the highaffinity IgE receptor in Wiskott-Aldrich syndrome protein-deficient mast cells. Int Immunol 2003; 15:1431-1440.
-
(2003)
Int Immunol
, vol.15
, pp. 1431-1440
-
-
Pivniouk, V.I.1
Snapper, S.B.2
Kettner, A.3
-
47
-
-
0032118427
-
Wiskott-Aldrich syndrome proteindeficient mice reveal a role for WASP in T but not B cell activation
-
Snapper SB, Rosen FS, Mizoguchi E, et al. Wiskott-Aldrich syndrome proteindeficient mice reveal a role for WASP in T but not B cell activation. Immunity 1998; 9:81-91.
-
(1998)
Immunity
, vol.9
, pp. 81-91
-
-
Snapper, S.B.1
Rosen, F.S.2
Mizoguchi, E.3
-
48
-
-
33846850600
-
Wiskott-Aldrich syndrome protein is • required for regulatory T cell homeostasis
-
The paper implicates defective Treg homeostasis and function to the autoimmunity seen in the Wiskott-Aldrich syndrome
-
Humblet-Baron S, Sather B, AnoverS, et al. Wiskott-Aldrich syndrome protein is • required for regulatory T cell homeostasis. J Clin Invest 2007; 117:407-418. The paper implicates defective Treg homeostasis and function to the autoimmunity seen in the Wiskott-Aldrich syndrome.
-
(2007)
J Clin Invest
, vol.117
, pp. 407-418
-
-
Humblet-Baron, S.1
Sather, B.2
AnoverS3
-
49
-
-
34250687456
-
-
Adriani M, Aoki J, Horai R, et al. Impaired in vitro regulatory T cell function • associated with Wiskott-Aldrich syndrome. Clin Immunol 2007; 124:41 -48. The paper implicates defective Treg homeostasis and function to the autoimmunity seen in the Wiskott-Aldrich syndrome.
-
Adriani M, Aoki J, Horai R, et al. Impaired in vitro regulatory T cell function • associated with Wiskott-Aldrich syndrome. Clin Immunol 2007; 124:41 -48. The paper implicates defective Treg homeostasis and function to the autoimmunity seen in the Wiskott-Aldrich syndrome.
-
-
-
-
50
-
-
33847161301
-
-
Maillard MH, Cotta-de-Almeida V, Takeshima F, et al. The Wiskott-Aldrich • syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells. J Exp Med 2007; 204:381 -391. The paper implicates defective Treg homeostasis and function to the autoimmunity seen in the Wiskott-Aldrich syndrome.
-
Maillard MH, Cotta-de-Almeida V, Takeshima F, et al. The Wiskott-Aldrich • syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells. J Exp Med 2007; 204:381 -391. The paper implicates defective Treg homeostasis and function to the autoimmunity seen in the Wiskott-Aldrich syndrome.
-
-
-
-
51
-
-
0034192223
-
Wiskott-Aldrich syndrome protein is necessary for efficient IgG-mediated phagocytosis
-
Lorenzi R, Brickell PM, Katz DR, et al. Wiskott-Aldrich syndrome protein is necessary for efficient IgG-mediated phagocytosis. Blood 2000; 95:2943- 2946.
-
(2000)
Blood
, vol.95
, pp. 2943-2946
-
-
Lorenzi, R.1
Brickell, P.M.2
Katz, D.R.3
-
52
-
-
0022494269
-
Cloning the gene for an inherited human disorder-chronic granulomatous disease-on the basis of its chromosomal location
-
Royer-Pokora B, Kunkel LM, Monaco AP, et al. Cloning the gene for an inherited human disorder-chronic granulomatous disease-on the basis of its chromosomal location. Nature 1986; 322:32-38.
-
(1986)
Nature
, vol.322
, pp. 32-38
-
-
Royer-Pokora, B.1
Kunkel, L.M.2
Monaco, A.P.3
-
53
-
-
0034040532
-
Chronic granulomatous disease. Report on a national registry of 368 patients
-
Winkelstein JA, Marino MC, Johnston RB Jr, et al. Chronic granulomatous disease. Report on a national registry of 368 patients. Medicine (Baltimore) 2000; 79:155-169.
-
(2000)
Medicine (Baltimore)
, vol.79
, pp. 155-169
-
-
Winkelstein, J.A.1
Marino, M.C.2
Johnston Jr, R.B.3
-
54
-
-
1542406446
-
NOX enzymes and the biology of reactive oxygen
-
Lambeth JD. NOX enzymes and the biology of reactive oxygen. Nat Rev Immunol 2004;4:181-189.
-
(2004)
Nat Rev Immunol
, vol.4
, pp. 181-189
-
-
Lambeth, J.D.1
-
56
-
-
0028893203
-
Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production
-
Pollock JD, Williams DA, Gifford MA, et al. Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production. Nat Genet 1995; 9:202-209.
-
(1995)
Nat Genet
, vol.9
, pp. 202-209
-
-
Pollock, J.D.1
Williams, D.A.2
Gifford, M.A.3
-
57
-
-
0347364678
-
Gene expression profiling provides insight into the pathophysiology of chronic granulomatous disease
-
Kobayashi SD, Voyich JM, Braughton KR, et al. Gene expression profiling provides insight into the pathophysiology of chronic granulomatous disease. J Immunol 2004; 172:636-643.
-
(2004)
J Immunol
, vol.172
, pp. 636-643
-
-
Kobayashi, S.D.1
Voyich, J.M.2
Braughton, K.R.3
|