-
1
-
-
1842529365
-
Clustering of autoimmune disease in parents of siblings from the type I diabetes Warren repository
-
Tait KF, Marshall T, Berman J, Carr-Smith J, Rowe B, Todd JA, Bain SC, Barnett AH, Gough SC 2004 Clustering of autoimmune disease in parents of siblings from the type I diabetes Warren repository. Diabet Med 21:358-362
-
(2004)
Diabet Med
, vol.21
, pp. 358-362
-
-
Tait, K.F.1
Marshall, T.2
Berman, J.3
Carr-Smith, J.4
Rowe, B.5
Todd, J.A.6
Bain, S.C.7
Barnett, A.H.8
Gough, S.C.9
-
4
-
-
0019811879
-
Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes
-
Neufeld M, Maclaren NK, Blizzard RM 1981 Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes. Medicine (Baltimore) 60:355-362
-
(1981)
Medicine (Baltimore)
, vol.60
, pp. 355-362
-
-
Neufeld, M.1
Maclaren, N.K.2
Blizzard, R.M.3
-
5
-
-
0032544004
-
Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases
-
Becker KG, Simon RM, Bailey-Wilson JE, Freidlin B, Biddison WE, McFarland HF, Trent JM 1998 Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases. Proc Natl Acad Sci USA 95:9979-9984
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 9979-9984
-
-
Becker, K.G.1
Simon, R.M.2
Bailey-Wilson, J.E.3
Freidlin, B.4
Biddison, W.E.5
McFarland, H.F.6
Trent, J.M.7
-
6
-
-
0029982537
-
Genetic analysis of autoimmune disease
-
Vyse TJ, Todd JA 1996 Genetic analysis of autoimmune disease. Cell 85:311-318
-
(1996)
Cell
, vol.85
, pp. 311-318
-
-
Vyse, T.J.1
Todd, J.A.2
-
7
-
-
0022656450
-
Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome
-
Maclaren NK, Riley WJ 1986 Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome. J Clin Endocrinol Metab 62:455-459
-
(1986)
J Clin Endocrinol Metab
, vol.62
, pp. 455-459
-
-
Maclaren, N.K.1
Riley, W.J.2
-
8
-
-
0016335428
-
HLA antigens as markers for disease susceptibility and autoimmunity in Graves' disease
-
Grumet FC, Payne RO, Konishi J, Kriss JP 1974 HLA antigens as markers for disease susceptibility and autoimmunity in Graves' disease. J Clin Endocrinol Metab 39:1115-1119
-
(1974)
J Clin Endocrinol Metab
, vol.39
, pp. 1115-1119
-
-
Grumet, F.C.1
Payne, R.O.2
Konishi, J.3
Kriss, J.P.4
-
9
-
-
0029038612
-
Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine autoimmune disease
-
Badenhoop K, Walfish PG, Rau H, Fischer S, Nicolay A, Bogner U, Schleusener H, Usadel KH 1995 Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine autoimmune disease. J Clin Endocrinol Metab 80:2112-2117
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 2112-2117
-
-
Badenhoop, K.1
Walfish, P.G.2
Rau, H.3
Fischer, S.4
Nicolay, A.5
Bogner, U.6
Schleusener, H.7
Usadel, K.H.8
-
10
-
-
0032776137
-
The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus
-
Vaidya B, Imrie H, Perros P, Young ET, Kelly WF, Carr D, Large DM, Toft AD, McCarthy MI, Kendall-Taylor P, Pearce SHS 1999 The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus. Hum Mol Genet 8:1195-1199
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1195-1199
-
-
Vaidya, B.1
Imrie, H.2
Perros, P.3
Young, E.T.4
Kelly, W.F.5
Carr, D.6
Large, D.M.7
Toft, A.D.8
McCarthy, M.I.9
Kendall-Taylor, P.10
Pearce, S.H.S.11
-
11
-
-
0033305040
-
Microsatellite polymorphism of the MHC class I chain-related (MIC-A and MIC-B) genes marks the risk for autoimmune Addison's disease
-
Gambelunghe G, Falorni A, Ghaderi M, Laureti S, Tortoioli C, Santeusanio F, Brunetti P, Sanjeevi CB 1999 Microsatellite polymorphism of the MHC class I chain-related (MIC-A and MIC-B) genes marks the risk for autoimmune Addison's disease. J Clin Endocrinol Metab 84:3701-3707
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 3701-3707
-
-
Gambelunghe, G.1
Falorni, A.2
Ghaderi, M.3
Laureti, S.4
Tortoioli, C.5
Santeusanio, F.6
Brunetti, P.7
Sanjeevi, C.B.8
-
12
-
-
38349098473
-
Analysis of extended human leukocyte antigen haplotype association with Addison's disease in three populations
-
Gombos Z, Hermann R, Kiviniemi M, Nejentsev S, Reimand K, Fadeyev V, Peterson P, Uibo R, Ilonen J 2007 Analysis of extended human leukocyte antigen haplotype association with Addison's disease in three populations. Eur J Endocrinol 157:757-761
-
(2007)
Eur J Endocrinol
, vol.157
, pp. 757-761
-
-
Gombos, Z.1
Hermann, R.2
Kiviniemi, M.3
Nejentsev, S.4
Reimand, K.5
Fadeyev, V.6
Peterson, P.7
Uibo, R.8
Ilonen, J.9
-
13
-
-
17744373659
-
Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease
-
Vaidya B, Imrie H, Geatch DR, Perros P, Ball SG, Baylis PH, Carr D, Hurel SJ, James RA, Kelly WF, Kemp EH, Young ET, Weetman AP, Kendall-Taylor P, Pearce SHS 2000 Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease. J Clin Endocrinol Metab 85:688-691
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 688-691
-
-
Vaidya, B.1
Imrie, H.2
Geatch, D.R.3
Perros, P.4
Ball, S.G.5
Baylis, P.H.6
Carr, D.7
Hurel, S.J.8
James, R.A.9
Kelly, W.F.10
Kemp, E.H.11
Young, E.T.12
Weetman, A.P.13
Kendall-Taylor, P.14
Pearce, S.H.S.15
-
14
-
-
3242732770
-
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease
-
Blomhoff A, Lie BA, Myhre AG, Kemp EH, Weetman AP, Akselsen HE, Huseby ES, Undlien DE 2004 Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease. J Clin Endocrinol Metab 89:3474-3476
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 3474-3476
-
-
Blomhoff, A.1
Lie, B.A.2
Myhre, A.G.3
Kemp, E.H.4
Weetman, A.P.5
Akselsen, H.E.6
Huseby, E.S.7
Undlien, D.E.8
-
15
-
-
8744266374
-
The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease
-
Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, Donaldson PT, Ball SG, James RA, Quinton R, Perros P, Pearce SH 2004 The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease. J Clin Endocrinol Metab 89:5862-5865
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5862-5865
-
-
Velaga, M.R.1
Wilson, V.2
Jennings, C.E.3
Owen, C.J.4
Herington, S.5
Donaldson, P.T.6
Ball, S.G.7
James, R.A.8
Quinton, R.9
Perros, P.10
Pearce, S.H.11
-
16
-
-
42549159759
-
Mutation screening of PTPN22: Association of the 1858T-allele with Addison's disease
-
Skinningsrud B, Husebye ES, Gervin K, Løvås K, Blomhoff A, Wolff AB, Kemp EH, Egeland T, Undlien DE 2008 Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease. Eur J Hum Genet 16:977-982
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 977-982
-
-
Skinningsrud, B.1
Husebye, E.S.2
Gervin, K.3
Løvås, K.4
Blomhoff, A.5
Wolff, A.B.6
Kemp, E.H.7
Egeland, T.8
Undlien, D.E.9
-
17
-
-
60349083325
-
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease
-
Roycroft M, Fichna M, McDonald D, Owen K, Zurawek M, Gryczyń ska M, Januszkiewicz-Lewandowska D, Fichna P, Cordell H, Donaldson P, Nowak J, Pearce S 2009 The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease. Clin Endocrinol (Oxf) 70:358-362
-
(2009)
Clin Endocrinol (Oxf)
, vol.70
, pp. 358-362
-
-
Roycroft, M.1
Fichna, M.2
McDonald, D.3
Owen, K.4
Zurawek, M.5
Gryczyń ska, M.6
Januszkiewicz-Lewandowska, D.7
Fichna, P.8
Cordell, H.9
Donaldson, P.10
Nowak, J.11
Pearce, S.12
-
18
-
-
33947546815
-
Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association
-
Owen CJ, Kelly H, Eden JA, Merriman ME, Pearce SH, Merriman TR 2007 Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association. J Clin Endocrinol Metab 92:1106-1111
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 1106-1111
-
-
Owen, C.J.1
Kelly, H.2
Eden, J.A.3
Merriman, M.E.4
Pearce, S.H.5
Merriman, T.R.6
-
19
-
-
18844366115
-
Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease
-
Hiratani H, Bowden DW, Ikegami S, Shirasawa S, Shimizu A, Iwatani Y, Akamizu T 2005 Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease. J Clin Endocrinol Metab 90:2898-2903
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 2898-2903
-
-
Hiratani, H.1
Bowden, D.W.2
Ikegami, S.3
Shirasawa, S.4
Shimizu, A.5
Iwatani, Y.6
Akamizu, T.7
-
20
-
-
33644790167
-
Association of the TSHR gene with Graves' disease: The first disease specific locus
-
Dechairo BM, Zabaneh D, Collins J, Brand O, Dawson GJ, Green AP, Mackay I, Franklyn JA, Connell JM, Wass JA, Wiersinga WM, Hegedus L, Brix T, Robinson BG, Hunt PJ, Weetman AP, Carey AH, Gough SC 2005 Association of the TSHR gene with Graves' disease: the first disease specific locus. Eur J Hum Genet 13:1223-1230
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 1223-1230
-
-
Dechairo, B.M.1
Zabaneh, D.2
Collins, J.3
Brand, O.4
Dawson, G.J.5
Green, A.P.6
Mackay, I.7
Franklyn, J.A.8
Connell, J.M.9
Wass, J.A.10
Wiersinga, W.M.11
Hegedus, L.12
Brix, T.13
Robinson, B.G.14
Hunt, P.J.15
Weetman, A.P.16
Carey, A.H.17
Gough, S.C.18
-
21
-
-
0344303638
-
Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease
-
Ban Y, Greenberg DA, Concepcion E, Skrabanek L, Villanueva R, Tomer Y 2003 Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease. Proc Natl Acad Sci USA 100:15119-15124
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 15119-15124
-
-
Ban, Y.1
Greenberg, D.A.2
Concepcion, E.3
Skrabanek, L.4
Villanueva, R.5
Tomer, Y.6
-
22
-
-
4444254102
-
A promoter polymorphism of the CYP27B1 gene is associated with Addison's disease, Hashimoto's thyroiditis, Graves' disease and type 1 diabetes mellitus in Germans
-
Lopez ER, Zwermann O, Segni M, Meyer G, Reincke M, Seissler J, Herwig J, Usadel KH, Badenhoop K 2004 A promoter polymorphism of the CYP27B1 gene is associated with Addison's disease, Hashimoto's thyroiditis, Graves' disease and type 1 diabetes mellitus in Germans. Eur J Endocrinol 151:193-197
-
(2004)
Eur J Endocrinol
, vol.151
, pp. 193-197
-
-
Lopez, E.R.1
Zwermann, O.2
Segni, M.3
Meyer, G.4
Reincke, M.5
Seissler, J.6
Herwig, J.7
Usadel, K.H.8
Badenhoop, K.9
-
23
-
-
21344464689
-
A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population
-
Jennings CE, Owen CJ, Wilson V, Pearce SH 2005 A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population. J Mol Endocrinol 34:859-863
-
(2005)
J Mol Endocrinol
, vol.34
, pp. 859-863
-
-
Jennings, C.E.1
Owen, C.J.2
Wilson, V.3
Pearce, S.H.4
-
24
-
-
51749098572
-
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency
-
Skinningsrud B, Husebye ES, Pearce SH, McDonald DO, Brandal K, Wolff AB, Løvås K, Egeland T, Undlien DE 2008 Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. J Clin Endocrinol Metab 93:3310-3317
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 3310-3317
-
-
Skinningsrud, B.1
Husebye, E.S.2
Pearce, S.H.3
McDonald, D.O.4
Brandal, K.5
Wolff, A.B.6
Løvås, K.7
Egeland, T.8
Undlien, D.E.9
-
25
-
-
33749540401
-
MHC2TA single nucleotide polymorphism and genetic risk for autoimmune adrenal insufficiency
-
Ghaderi M, Gambelunghe G, Tortoioli C, Brozzetti A, Jatta K, Gharizadeh B, De Bellis A, Pecori Giraldi F, Terzolo M, Betterle C, Falorni A 2006 MHC2TA single nucleotide polymorphism and genetic risk for autoimmune adrenal insufficiency. J Clin Endocrinol Metab 91:4107-4111
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 4107-4111
-
-
Ghaderi, M.1
Gambelunghe, G.2
Tortoioli, C.3
Brozzetti, A.4
Jatta, K.5
Gharizadeh, B.6
De Bellis, A.7
Pecori Giraldi, F.8
Terzolo, M.9
Betterle, C.10
Falorni, A.11
-
26
-
-
61849088045
-
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
-
Magitta NF, Bøe Wolff AS, Johansson S, Skinningsrud B, Lie BA, Myhr KM, Undlien DE, Joner G, Njølstad PR, Kvien TK, Førre Ø, Knappskog PM, Husebye ES 2009 A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes. Genes Immun. 10:120-124
-
(2009)
Genes Immun
, vol.10
, pp. 120-124
-
-
Magitta, N.F.1
Bøe Wolff, A.S.2
Johansson, S.3
Skinningsrud, B.4
Lie, B.A.5
Myhr, K.M.6
Undlien, D.E.7
Joner, G.8
Njølstad, P.R.9
Kvien, T.K.10
Førre, Ø.11
Knappskog, P.M.12
Husebye, E.S.13
-
27
-
-
0037307930
-
Blockade of programmed death-1 ligands on dendritic cells enhances T cell activation and cytokine production
-
Brown JA, Dorfman DM, Ma FR, Sullivan EL, Munoz O, Wood CR, Greenfield EA, Freeman GJ 2003 Blockade of programmed death-1 ligands on dendritic cells enhances T cell activation and cytokine production. J Immunol 170:1257-1266
-
(2003)
J Immunol
, vol.170
, pp. 1257-1266
-
-
Brown, J.A.1
Dorfman, D.M.2
Ma, F.R.3
Sullivan, E.L.4
Munoz, O.5
Wood, C.R.6
Greenfield, E.A.7
Freeman, G.J.8
-
28
-
-
13244277850
-
-
Prokunina L, Castillejo-Ló pez C, Oberg F, Gunnarsson I, Berg L, Magnusson V, Brookes AJ, Tentler D, Kristjansdó ttir H, Grö ndal G, Bolstad AI, Svenungsson E, Lundberg I, Sturfelt G, Jö nssen A, Truedsson L, Lima G, Alcocer-Varela J, Jonsson R, Gyllensten UB, Harley JB, Alarcón-Segovia D, Steinsson K, Alarcón-Riquelme ME 2002 A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nat Genet 32:666-669
-
Prokunina L, Castillejo-Ló pez C, Oberg F, Gunnarsson I, Berg L, Magnusson V, Brookes AJ, Tentler D, Kristjansdó ttir H, Grö ndal G, Bolstad AI, Svenungsson E, Lundberg I, Sturfelt G, Jö nssen A, Truedsson L, Lima G, Alcocer-Varela J, Jonsson R, Gyllensten UB, Harley JB, Alarcón-Segovia D, Steinsson K, Alarcón-Riquelme ME 2002 A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nat Genet 32:666-669
-
-
-
-
29
-
-
0344099132
-
Association of a putative regulatory polymorphism in the PD-1 gene with susceptibility to type 1 diabetes
-
Nielsen C, Hansen D, Husby S, Jacobsen BB, Lillevang ST 2003 Association of a putative regulatory polymorphism in the PD-1 gene with susceptibility to type 1 diabetes. Tissue Antigens 62:492-497
-
(2003)
Tissue Antigens
, vol.62
, pp. 492-497
-
-
Nielsen, C.1
Hansen, D.2
Husby, S.3
Jacobsen, B.B.4
Lillevang, S.T.5
-
30
-
-
2642575164
-
Association of the PD-1.3A allele of the PDCD1 gene in patients with rheumatoid arthritis negative for rheumatoid factor and the shared epitope
-
Prokunina L, Padyukov L, Bennet A, de Faire U, Wiman B, Prince J, Alfredsson L, Klareskog L, Alarcó n-Riquelme M 2004 Association of the PD-1.3A allele of the PDCD1 gene in patients with rheumatoid arthritis negative for rheumatoid factor and the shared epitope. Arthritis Rheum 50:1770-1773
-
(2004)
Arthritis Rheum
, vol.50
, pp. 1770-1773
-
-
Prokunina, L.1
Padyukov, L.2
Bennet, A.3
de Faire, U.4
Wiman, B.5
Prince, J.6
Alfredsson, L.7
Klareskog, L.8
Alarcó n-Riquelme, M.9
-
31
-
-
34547756980
-
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility
-
Sutherland A, Davies J, Owen CJ, Vaikkakara S, Walker C, Cheetham TD, James RA, Perros P, Donaldson PT, Cordell HJ, Quinton R, Pearce SH 2007 Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility. J Clin Endocrinol Metab 92:3338-3341
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 3338-3341
-
-
Sutherland, A.1
Davies, J.2
Owen, C.J.3
Vaikkakara, S.4
Walker, C.5
Cheetham, T.D.6
James, R.A.7
Perros, P.8
Donaldson, P.T.9
Cordell, H.J.10
Quinton, R.11
Pearce, S.H.12
-
32
-
-
44949142100
-
Association of an A/C single nucleotide polymorphism in programmed cell death ligand 1 gene with Graves' disease in Japanese patients
-
Hayashi M, Kouki T, Takasu N, Sunagawa S, Komiya I 2008 Association of an A/C single nucleotide polymorphism in programmed cell death ligand 1 gene with Graves' disease in Japanese patients. Eur J Endocrinol 158:817-822
-
(2008)
Eur J Endocrinol
, vol.158
, pp. 817-822
-
-
Hayashi, M.1
Kouki, T.2
Takasu, N.3
Sunagawa, S.4
Komiya, I.5
-
33
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
The International HapMap Consortium
-
The International HapMap Consortium 2007. A second generation human haplotype map of over 3.1 million SNPs. Nature 449:851-861
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
-
34
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F 2003 Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 25:115-221
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-221
-
-
Dudbridge, F.1
-
35
-
-
62849101614
-
Genetics of type 1 diabetes and autoimmune thyroid disease
-
Pearce SH, Merriman TR 2009 Genetics of type 1 diabetes and autoimmune thyroid disease. Endocrinol Metab Clin North Am 38:289-301
-
(2009)
Endocrinol Metab Clin North Am
, vol.38
, pp. 289-301
-
-
Pearce, S.H.1
Merriman, T.R.2
-
36
-
-
33645846313
-
Tissue expression of PD-L1 mediates peripheral T cell tolerance
-
Keir ME, Liang SC, Guleria I, Latchman YE, Qipo A, Albacker LA, Koulmanda M, Freeman GJ, Sayegh MH, Sharpe AH 2006 Tissue expression of PD-L1 mediates peripheral T cell tolerance. J Exp Med 203:883-895
-
(2006)
J Exp Med
, vol.203
, pp. 883-895
-
-
Keir, M.E.1
Liang, S.C.2
Guleria, I.3
Latchman, Y.E.4
Qipo, A.5
Albacker, L.A.6
Koulmanda, M.7
Freeman, G.J.8
Sayegh, M.H.9
Sharpe, A.H.10
|