-
2
-
-
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
-
3
-
-
43249086529
-
Infections in 252 patients with common variable immunodeficiency
-
Oksenhendler E, Gerard L, Fieschi C, et al. Infections in 252 patients with common variable immunodeficiency. Clin Infect Dis 2008;46: 1547-54.
-
(2008)
Clin Infect Dis
, vol.46
, pp. 1547-54
-
-
Oksenhendler, E.1
Gerard, L.2
Fieschi, C.3
-
4
-
-
34249048637
-
Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency
-
Quinti I, Soresina A, Spadaro G, et al. Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency. J Clin Immunol 2007;27:308-16.
-
(2007)
J Clin Immunol
, vol.27
, pp. 308-16
-
-
Quinti, I.1
Soresina, A.2
Spadaro, G.3
-
5
-
-
22244489355
-
Clinical and im-munological features of 65 Iranian patients with common variable immunodeficiency
-
Aghamohammadi A, Farhoudi A, Moin M, et al. Clinical and im-munological features of 65 Iranian patients with common variable immunodeficiency. Clin Diagn Lab Immunol 2005;12:825-32.
-
(2005)
Clin Diagn Lab Immunol
, vol.12
, pp. 825-32
-
-
Aghamohammadi, A.1
Farhoudi, A.2
Moin, M.3
-
6
-
-
47749137360
-
Clinical and immunologic features of pediatric patients with common variable immunodeficiency and respiratory complications
-
Aydogan M, Eifan AO, Gocmen I, et al. Clinical and immunologic features of pediatric patients with common variable immunodeficiency and respiratory complications. J Investig Allergol Clin Immunol 2008; 18:260-5.
-
(2008)
J Investig Allergol Clin Immunol
, vol.18
, pp. 260-5
-
-
Aydogan, M.1
Eifan, A.O.2
Gocmen, I.3
-
7
-
-
0035049393
-
Diagnostic findings in 95 Finnish patients with common variable immunodeficiency
-
Kainulainen L, Nikoskelainen J, Ruuskanen O. Diagnostic findings in 95 Finnish patients with common variable immunodeficiency. J Clin Immunol 2001;21:145-9.
-
(2001)
J Clin Immunol
, vol.21
, pp. 145-9
-
-
Kainulainen, L.1
Nikoskelainen, J.2
Ruuskanen, O.3
-
8
-
-
63149147362
-
Common variable immunodeficiency: 20-year experience at a single centre
-
Llobet MP, Soler-Palacin P, Detkova D, et al. Common variable immunodeficiency: 20-year experience at a single centre. Pediatr Allergy Immunol 2009;20:113-8.
-
(2009)
Pediatr Allergy Immunol
, vol.20
, pp. 113-8
-
-
Llobet, M.P.1
Soler-Palacin, P.2
Detkova, D.3
-
9
-
-
36448992684
-
Gastrointestinal tract pathology in patients with common variable immunodeficiency (CVID): A clinicopathologic study and review
-
Daniels JA, Lederman HM, Maitra A, et al. Gastrointestinal tract pathology in patients with common variable immunodeficiency (CVID): a clinicopathologic study and review. Am J Surg Pathol 2007;31:1800-12.
-
(2007)
Am J Surg Pathol
, vol.31
, pp. 1800-12
-
-
Daniels, J.A.1
Lederman, H.M.2
Maitra, A.3
-
10
-
-
34848833281
-
Gastrointestinal manifestations in patients with common variable immunodeficiency
-
Khodadad A, Aghamohammadi A, Parvaneh N, et al. Gastrointestinal manifestations in patients with common variable immunodeficiency. Dig Dis Sci 2007;52:2977-83.
-
(2007)
Dig Dis Sci
, vol.52
, pp. 2977-83
-
-
Khodadad, A.1
Aghamohammadi, A.2
Parvaneh, N.3
-
11
-
-
0037253625
-
Duodenal pathology and clinical-immunological implications in common variable immunodeficiency patients
-
Luzi G, Zullo A, Iebba F, et al. Duodenal pathology and clinical-immunological implications in common variable immunodeficiency patients. Am J Gastroenterol 2003;98:118-21.
-
(2003)
Am J Gastroenterol
, vol.98
, pp. 118-21
-
-
Luzi, G.1
Zullo, A.2
Iebba, F.3
-
12
-
-
0029813737
-
Gastrointestinal pathology in patients with common variable immunodeficiency and X-linked agammaglobulinemia
-
Washington K, Stenzel TT, Buckley RH, et al. Gastrointestinal pathology in patients with common variable immunodeficiency and X-linked agammaglobulinemia. Am J Surg Pathol 1996;20:1240-52.
-
(1996)
Am J Surg Pathol
, vol.20
, pp. 1240-52
-
-
Washington, K.1
Stenzel, T.T.2
Buckley, R.H.3
-
13
-
-
0032966062
-
Gastric pathology in patients with common variable immunodeficiency
-
Zullo A, Romiti A, Rinaldi V, et al. Gastric pathology in patients with common variable immunodeficiency. Gut 1999;45:77-81.
-
(1999)
Gut
, vol.45
, pp. 77-81
-
-
Zullo, A.1
Romiti, A.2
Rinaldi, V.3
-
14
-
-
0015900093
-
Primary immunodeficiency diseases and cancer: The immunodeficiency-cancer registry
-
Kersey JH, Spector BD, Good RA. Primary immunodeficiency diseases and cancer: the immunodeficiency-cancer registry. Int J Cancer 1973;12:333-47.
-
(1973)
Int J Cancer
, vol.12
, pp. 333-47
-
-
Kersey, J.H.1
Spector, B.D.2
Good, R.A.3
-
15
-
-
18744411225
-
Cancer risk among patients with IgA deficiency or common variable immunodeficiency and their relatives: A combined Danish and Swedish study
-
Mellemkjaer L, Hammarstrom L, Andersen V, et al. Cancer risk among patients with IgA deficiency or common variable immunodeficiency and their relatives: a combined Danish and Swedish study. Clin Exp Immunol 2002;130:495-500.
-
(2002)
Clin Exp Immunol
, vol.130
, pp. 495-500
-
-
Mellemkjaer, L.1
Hammarstrom, L.2
Andersen, V.3
-
16
-
-
0017073215
-
Idiopathic late-onset immu-noglobulin deficiency. Clinical observations in 50 patients
-
Hermans PE, Diaz-Buxo JA, Stobo JD. Idiopathic late-onset immu-noglobulin deficiency. Clinical observations in 50 patients. Am J Med 1976;61:221-37.
-
(1976)
Am J Med
, vol.61
, pp. 221-37
-
-
Hermans, P.E.1
Diaz-Buxo, J.A.2
Stobo, J.D.3
-
17
-
-
0027538145
-
Primary hypogammaglobulinaemia: A survey of clinical manifestations and complications
-
Hermaszewski RA, Webster AD. Primary hypogammaglobulinaemia: a survey of clinical manifestations and complications. Q J Med 1993; 86:31-42.
-
(1993)
Q J Med
, vol.86
, pp. 31-42
-
-
Hermaszewski, R.A.1
Webster, A.D.2
-
18
-
-
0021915329
-
Prospective study of cancer in patients with hypogammaglobulinaemia
-
Kinlen LJ, Webster AD, Bird AG, et al. Prospective study of cancer in patients with hypogammaglobulinaemia. Lancet 1985;1:263-6.
-
(1985)
Lancet
, vol.1
, pp. 263-6
-
-
Kinlen, L.J.1
Webster, A.D.2
Bird, A.G.3
-
20
-
-
0242708853
-
Lymphoproliferative disease in antibody deficiency: A multi-centre study
-
Gompels MM, Hodges E, Lock RJ, et al. Lymphoproliferative disease in antibody deficiency: a multi-centre study. Clin Exp Immunol 2003; 134:314-20.
-
(2003)
Clin Exp Immunol
, vol.134
, pp. 314-20
-
-
Gompels, M.M.1
Hodges, E.2
Lock, R.J.3
-
21
-
-
0034757950
-
Physiology of IgA and IgA deficiency
-
Cunningham-Rundles C. Physiology of IgA and IgA deficiency. J Clin Immunol 2001;21:303-9.
-
(2001)
J Clin Immunol
, vol.21
, pp. 303-9
-
-
Cunningham-Rundles, C.1
-
22
-
-
69949147603
-
Selective IgA deficiency in early life: Association to infections and allergic diseases during childhood
-
Janzi M, Kull I, Sjoberg R, et al. Selective IgA deficiency in early life: association to infections and allergic diseases during childhood. Clin Immunol 2009;133:78-85.
-
(2009)
Clin Immunol
, vol.133
, pp. 78-85
-
-
Janzi, M.1
Kull, I.2
Sjoberg, R.3
-
23
-
-
0022447364
-
Susceptibility to infections in children with selective IgA-and IgA-IgG subclass deficiency
-
Morell A, Muehlheim E, Schaad U, et al. Susceptibility to infections in children with selective IgA-and IgA-IgG subclass deficiency. Eur J Pediatr 1986;145:199-203.
-
(1986)
Eur J Pediatr
, vol.145
, pp. 199-203
-
-
Morell, A.1
Muehlheim, E.2
Schaad, U.3
-
24
-
-
0015134807
-
IgA deficiency in children. A clinical study with special reference to intestinal findings
-
Savilahti E, Pelkonen P, Visakorpi JK. IgA deficiency in children. A clinical study with special reference to intestinal findings. Arch Dis Child 1971;46:665-70.
-
(1971)
Arch Dis Child
, vol.46
, pp. 665-70
-
-
Savilahti, E.1
Pelkonen, P.2
Visakorpi, J.K.3
-
25
-
-
0015062976
-
Selective IgA deficiency: Presentation of 30 cases and a review of the literature
-
Ammann AJ, Hong R. Selective IgA deficiency: presentation of 30 cases and a review of the literature. Medicine (Baltimore) 1971;50: 223-36.
-
(1971)
Medicine (Baltimore)
, vol.50
, pp. 223-36
-
-
Ammann, A.J.1
Hong, R.2
-
26
-
-
0019719802
-
Primary immunodeficiency syndrome in Japan. I. Overview of a nationwide survey on primary immunodeficiency syndrome
-
Hayakawa H, Iwata T, Yata J, et al. Primary immunodeficiency syndrome in Japan. I. Overview of a nationwide survey on primary immunodeficiency syndrome. J Clin Immunol 1981;1:31-9.
-
(1981)
J Clin Immunol
, vol.1
, pp. 31-9
-
-
Hayakawa, H.1
Iwata, T.2
Yata, J.3
-
27
-
-
0020400363
-
Primary immunodeficiency disorders in Sweden: Cases among children 1974-1979
-
Fasth A. Primary immunodeficiency disorders in Sweden: cases among children, 1974-1979. J Clin Immunol 1982;2:86-92.
-
(1982)
J Clin Immunol
, vol.2
, pp. 86-92
-
-
Fasth, A.1
-
28
-
-
0021036687
-
Primary immunodeficiency syndromes in Italy: A report of the national register in children and adults
-
Luzi G, Businco L, Aiuti F. Primary immunodeficiency syndromes in Italy: a report of the national register in children and adults. J Clin Immunol 1983;3:316-20.
-
(1983)
J Clin Immunol
, vol.3
, pp. 316-20
-
-
Luzi, G.1
Businco, L.2
Aiuti, F.3
-
29
-
-
0024209085
-
Primary immunodeficiencies in Switzerland: First report of the national registry in adults and children
-
Ryser O, Morell A, Hitzig WH. Primary immunodeficiencies in Switzerland: first report of the national registry in adults and children. J Clin Immunol 1988;8:479-85.
-
(1988)
J Clin Immunol
, vol.8
, pp. 479-85
-
-
Ryser, O.1
Morell, A.2
Hitzig, W.H.3
-
30
-
-
59449092473
-
IgA deficiency: Correlation between clinical and immunological phenotypes
-
Aghamohammadi A, Cheraghi T, Gharagozlou M, et al. IgA deficiency: correlation between clinical and immunological phenotypes. J Clin Immunol 2009;29:130-6.
-
(2009)
J Clin Immunol
, vol.29
, pp. 130-6
-
-
Aghamohammadi, A.1
Cheraghi, T.2
Gharagozlou, M.3
-
31
-
-
0025896040
-
Clinical manifestations in selective IgA deficiency in childhood. A follow-up report
-
De Laat PC, Weemaes CM, Gonera R, et al. Clinical manifestations in selective IgA deficiency in childhood. A follow-up report. Acta Paediatr Scand 1991;80:798-804.
-
(1991)
Acta Paediatr Scand
, vol.80
, pp. 798-804
-
-
De Laat, P.C.1
Weemaes, C.M.2
Gonera, R.3
-
32
-
-
0021042433
-
Recurrent infections in children with "selective" IgA deficiency: Association with IgG2 and IgG4 deficiency
-
Ugazio AG, Out TA, Plebani A, et al. Recurrent infections in children with "selective" IgA deficiency: association with IgG2 and IgG4 deficiency. Birth Defects Orig Artic Ser 1983;19:169-71.
-
(1983)
Birth Defects Orig Artic ser
, vol.19
, pp. 169-71
-
-
Ugazio, A.G.1
Out, T.A.2
Plebani, A.3
-
33
-
-
0018877395
-
Selective IgA deficiency: Clinical and immunological evaluation of 50 pediatric patients
-
Burgio GR, Duse M, Monafo V, et al. Selective IgA deficiency: clinical and immunological evaluation of 50 pediatric patients. Eur J Pediatr 1980;133:101-6.
-
(1980)
Eur J Pediatr
, vol.133
, pp. 101-6
-
-
Burgio, G.R.1
Duse, M.2
Monafo, V.3
-
34
-
-
0014694096
-
Correlation of milk precipitins with IgA deficiency
-
Buckley RH, Dees SC. Correlation of milk precipitins with IgA deficiency. N Engl J Med 1969;281:465-9.
-
(1969)
N Engl J Med
, vol.281
, pp. 465-9
-
-
Buckley, R.H.1
Dees, S.C.2
-
35
-
-
2042536683
-
Burden of allergic disease in the UK: Secondary analyses of national databases
-
Gupta R, Sheikh A, Strachan DP, et al. Burden of allergic disease in the UK: secondary analyses of national databases. Clin Exp Allergy 2004; 34:520-6.
-
(2004)
Clin Exp Allergy
, vol.34
, pp. 520-6
-
-
Gupta, R.1
Sheikh, A.2
Strachan, D.P.3
-
36
-
-
0021822070
-
Levels of immunoglobulin G, M, A, and e at various ages in allergic and nonallergic black and white individuals
-
Grundbacher FJ, Massie FS. Levels of immunoglobulin G, M, A, and E at various ages in allergic and nonallergic black and white individuals. J Allergy Clin Immunol 1985;75:651-8.
-
(1985)
J Allergy Clin Immunol
, vol.75
, pp. 651-8
-
-
Grundbacher, F.J.1
Massie, F.S.2
-
37
-
-
0023105593
-
Comparison of the frequency of atopic diseases in children with severe and partial IgA deficiency
-
Plebani A, Monafo V, Ugazio AG, et al. Comparison of the frequency of atopic diseases in children with severe and partial IgA deficiency. Int Arch Allergy Appl Immunol 1987;82:485-6.
-
(1987)
Int Arch Allergy Appl Immunol
, vol.82
, pp. 485-6
-
-
Plebani, A.1
Monafo, V.2
Ugazio, A.G.3
-
38
-
-
0014365564
-
Selective hypogammaglobulinemia in rheumatoid arthritis
-
Cassidy JT, Burt A. Selective hypogammaglobulinemia in rheumatoid arthritis. Univ Mich Med Cent J 1968:241-243.
-
(1968)
Univ Mich Med Cent J
, pp. 241-243
-
-
Cassidy, J.T.1
Burt, A.2
-
39
-
-
0015373806
-
Serum immunoglobulins in systemic lupus erythematosus
-
Alarcon-Segovia D, Fishbein E. Serum immunoglobulins in systemic lupus erythematosus. Clin Sci 1972;43:121-31.
-
(1972)
Clin Sci
, vol.43
, pp. 121-31
-
-
Alarcon-Segovia, D.1
Fishbein, E.2
-
42
-
-
0017114834
-
Antibodies to nucleic acids in congenital immune deficiency states
-
Gershwin ME, Blaese RM, Steinberg AD, et al. Antibodies to nucleic acids in congenital immune deficiency states. J Pediatr 1976;89: 377-81.
-
(1976)
J Pediatr
, vol.89
, pp. 377-81
-
-
Gershwin, M.E.1
Blaese, R.M.2
Steinberg, A.D.3
-
43
-
-
0014815641
-
Juvenile rheumatoid arthritis\a serologic survey of 200 consecutive patients
-
Bluestone R, Goldberg LS, Katz RM, et al. Juvenile rheumatoid arthritis\a serologic survey of 200 consecutive patients. J Pediatr 1970;77:98-102.
-
(1970)
J Pediatr
, vol.77
, pp. 98-102
-
-
Bluestone, R.1
Goldberg, L.S.2
Katz, R.M.3
-
44
-
-
0015254039
-
Juvenile rheumatoid arthritis. Cellularhypersensitivity and selective IgA deficiency
-
Panush RS, Bianco NE, Schur PH, et al. Juvenile rheumatoid arthritis. Cellularhypersensitivity and selective IgA deficiency. Clin Exp Immunol 1972;10:103-15.
-
(1972)
Clin Exp Immunol
, vol.10
, pp. 103-15
-
-
Panush, R.S.1
Bianco, N.E.2
Schur, P.H.3
-
45
-
-
0015766924
-
Levels of serum immu-noglobulins in juvenile rheumatoid arthritis
-
Salmi TT, Schmidt E, Laaksonen AL, et al. Levels of serum immu-noglobulins in juvenile rheumatoid arthritis. Ann Clin Res 1973; 5:395-7.
-
(1973)
Ann Clin Res
, vol.5
, pp. 395-7
-
-
Salmi, T.T.1
Schmidt, E.2
Laaksonen, A.L.3
-
46
-
-
0018775238
-
IgA deficiency in juvenile chronic polyarthritis
-
Barkley DO, Hohermuth HJ, Howard A, et al. IgA deficiency in juvenile chronic polyarthritis. J Rheumatol 1979;6:219-24.
-
(1979)
J Rheumatol
, vol.6
, pp. 219-24
-
-
Barkley, D.O.1
Hohermuth, H.J.2
Howard, A.3
-
47
-
-
0021079288
-
Persistent and transient IgA deficiency in juvenile rheumatoid arthritis
-
Pelkonen P, Savilahti E, Makela AL. Persistent and transient IgA deficiency in juvenile rheumatoid arthritis. Scand J Rheumatol 1983; 12:273-9.
-
(1983)
Scand J Rheumatol
, vol.12
, pp. 273-9
-
-
Pelkonen, P.1
Savilahti, E.2
Makela, A.L.3
-
48
-
-
0015015023
-
Family studies in individuals with selective absence of gamma-A-globulin
-
Natvig JB, Harboe M, Fausa O, et al. Family studies in individuals with selective absence of gamma-A-globulin. Clin Exp Immunol 1971; 8:229-36.
-
(1971)
Clin Exp Immunol
, vol.8
, pp. 229-36
-
-
Natvig, J.B.1
Harboe, M.2
Fausa, O.3
-
49
-
-
0030665561
-
Celiac disease and selective immunoglobulin A deficiency
-
Cataldo F, Marino V, Bottaro G, et al. Celiac disease and selective immunoglobulin A deficiency. J Pediatr 1997;131:306-8.
-
(1997)
J Pediatr
, vol.131
, pp. 306-8
-
-
Cataldo, F.1
Marino, V.2
Bottaro, G.3
-
51
-
-
47549092356
-
Celiac disease and IgA deficiency: Complications of serological testing approaches encountered in the clinic
-
McGowan KE, Lyon ME, Butzner JD. Celiac disease and IgA deficiency: complications of serological testing approaches encountered in the clinic. Clin Chem 2008;54:1203-9.
-
(2008)
Clin Chem
, vol.54
, pp. 1203-9
-
-
McGowan, K.E.1
Lyon, M.E.2
Butzner, J.D.3
-
52
-
-
0242266471
-
Elevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiency
-
Korponay-Szabo IR, Dahlbom I, Laurila K, et al. Elevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiency. Gut 2003;52: 1567-71.
-
(2003)
Gut
, vol.52
, pp. 1567-71
-
-
Korponay-Szabo, I.R.1
Dahlbom, I.2
Laurila, K.3
-
53
-
-
0023583602
-
Deficiency of immunoglobulin A
-
Klemola T. Deficiency of immunoglobulin A. Ann Clin Res 1987;19: 248-57.
-
(1987)
Ann Clin Res
, vol.19
, pp. 248-57
-
-
Klemola, T.1
-
54
-
-
0023908418
-
Immunohistochemical findings in the intestine of IgA-deficient persons: Number of intraepithelial T lymphocytes is increased
-
Klemola T. Immunohistochemical findings in the intestine of IgA-deficient persons: number of intraepithelial T lymphocytes is increased. J Pediatr Gastroenterol Nutr 1988;7:537-43.
-
(1988)
J Pediatr Gastroenterol Nutr
, vol.7
, pp. 537-43
-
-
Klemola, T.1
-
55
-
-
0030457134
-
Prevalence and diagnosis of celiac disease in IgA-deficient children
-
Meini A, Pillan NM, Villanacci V, et al. Prevalence and diagnosis of celiac disease in IgA-deficient children. Ann Allergy Asthma Immunol 1996;77:333-6.
-
(1996)
Ann Allergy Asthma Immunol
, vol.77
, pp. 333-6
-
-
Meini, A.1
Pillan, N.M.2
Villanacci, V.3
-
56
-
-
0036843842
-
Celiac disease and immunoglobulin a deficiency: How effective are the serological methods of diagnosis?
-
Kumar V, Jarzabek-Chorzelska M, Sulej J, et al. Celiac disease and immunoglobulin a deficiency: how effective are the serological methods of diagnosis? Clin Diagn Lab Immunol 2002;9:1295-300.
-
(2002)
Clin Diagn Lab Immunol
, vol.9
, pp. 1295-300
-
-
Kumar, V.1
Jarzabek-Chorzelska, M.2
Sulej, J.3
-
57
-
-
51849093138
-
Progression of selective IgA deficiency to common variable immunodeficiency
-
Aghamohammadi A, Mohammadi J, Parvaneh N, et al. Progression of selective IgA deficiency to common variable immunodeficiency. Int Arch Allergy Immunol 2008;147:87-92.
-
(2008)
Int Arch Allergy Immunol
, vol.147
, pp. 87-92
-
-
Aghamohammadi, A.1
Mohammadi, J.2
Parvaneh, N.3
-
59
-
-
0029839187
-
Development of a common variable immunodeficiency in IgA-deficient patients
-
Espanol T, Catala M, Hernandez M, et al. Development of a common variable immunodeficiency in IgA-deficient patients. Clin Immunol Immunopathol 1996;80:333-5.
-
(1996)
Clin Immunol Immunopathol
, vol.80
, pp. 333-5
-
-
Espanol, T.1
Catala, M.2
Hernandez, M.3
-
60
-
-
0030786740
-
Progressive immunodeficiency in a patient with IgA deficiency
-
Gutierrez MG, Kirkpatrick CH. Progressive immunodeficiency in a patient with IgA deficiency. Ann Allergy Asthma Immunol 1997;79: 297-301.
-
(1997)
Ann Allergy Asthma Immunol
, vol.79
, pp. 297-301
-
-
Gutierrez, M.G.1
Kirkpatrick, C.H.2
-
61
-
-
0032806334
-
Diagnostic criteria for primary immunodeficiencies Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)
-
Conley ME, Notarangelo LD, Etzioni A. Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). Clin Immunol 1999;93:190-7.
-
(1999)
Clin Immunol
, vol.93
, pp. 190-7
-
-
Conley, M.E.1
Notarangelo, L.D.2
Etzioni, A.3
-
62
-
-
0034040532
-
Chronic granu-lomatous disease. Report on a national registry of 368 patients
-
Winkelstein JA, Marino MC, Johnston RB Jr et al. Chronic granu-lomatous disease. Report on a national registry of 368 patients. Medicine (Baltimore) 2000;79:155-69.
-
(2000)
Medicine (Baltimore)
, vol.79
, pp. 155-69
-
-
Winkelstein, J.A.1
Marino, M.C.2
Johnston Jr., R.B.3
-
63
-
-
70449140148
-
A fatal granulomatosus of childhood: The clinical study of a new syndrome
-
Berendes H, Bridges RA, Good RA. A fatal granulomatosus of childhood: the clinical study of a new syndrome. Minn Med 1957; 40:309-12.
-
(1957)
Minn Med
, vol.40
, pp. 309-12
-
-
Berendes, H.1
Bridges, R.A.2
Good, R.A.3
-
64
-
-
70449235654
-
A fatal granulomatous disease of childhood; The clinical, pathological, and laboratory features of a new syndrome
-
Bridges RA, Berendes H, Good RA. A fatal granulomatous disease of childhood; the clinical, pathological, and laboratory features of a new syndrome. AMA J Dis Child 1959;97:387-408.
-
(1959)
AMA J Dis Child
, vol.97
, pp. 387-408
-
-
Bridges, R.A.1
Berendes, H.2
Good, R.A.3
-
65
-
-
65349179624
-
Chronic granulo-matous disease: The European experience
-
Van Den Berg JM, van Koppen E, Ahlin A, et al. Chronic granulo-matous disease: the European experience. PLoS One 2009;4:e5234.
-
(2009)
PLoS One
, vol.4
-
-
Van Den Berg, J.M.1
Van Koppen, E.2
Ahlin, A.3
-
66
-
-
0029565532
-
Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden
-
Ahlin A, De Boer M, Roos D, et al. Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden. Acta Paediatr 1995;84:1386-94.
-
(1995)
Acta Paediatr
, vol.84
, pp. 1386-94
-
-
Ahlin, A.1
De Boer, M.2
Roos, D.3
-
67
-
-
54249141863
-
Clinical features and prognoses of 23 patients with chronic granulomatous disease followed for 21 years by a single hospital in Japan
-
Kobayashi S, Murayama S, Takanashi S, et al. Clinical features and prognoses of 23 patients with chronic granulomatous disease followed for 21 years by a single hospital in Japan. Eur J Pediatr 2008;167: 1389-94.
-
(2008)
Eur J Pediatr
, vol.167
, pp. 1389-94
-
-
Kobayashi, S.1
Murayama, S.2
Takanashi, S.3
-
68
-
-
0033739697
-
Long-term follow-up and outcome of 39 patients with chronic granulomatous disease
-
Liese J, Kloos S, Jendrossek V, et al. Long-term follow-up and outcome of 39 patients with chronic granulomatous disease. J Pediatr 2000;137:687-93.
-
(2000)
J Pediatr
, vol.137
, pp. 687-93
-
-
Liese, J.1
Kloos, S.2
Jendrossek, V.3
-
69
-
-
37849008955
-
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study
-
Martire B, Rondelli R, Soresina A, et al. Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study. Clin Immunol 2008;126:155-64.
-
(2008)
Clin Immunol
, vol.126
, pp. 155-64
-
-
Martire, B.1
Rondelli, R.2
Soresina, A.3
-
71
-
-
51249086031
-
Chronic granulomatous disease in Israel: Clinical, functional and molecular studies of 38 patients
-
Wolach B, Gavrieli R, de Boer M, et al. Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patients. Clin Immunol 2008;129:103-14.
-
(2008)
Clin Immunol
, vol.129
, pp. 103-14
-
-
Wolach, B.1
Gavrieli, R.2
De Boer, M.3
-
72
-
-
42049108433
-
Special article: Chronic granulomatous disease in the United Kingdom and Ireland: A comprehensive national patient-based registry
-
Jones LB, McGrogan P, Flood TJ, et al. Special article: chronic granulomatous disease in the United Kingdom and Ireland: a comprehensive national patient-based registry. Clin Exp Immunol 2008; 152:211-8.
-
(2008)
Clin Exp Immunol
, vol.152
, pp. 211-8
-
-
Jones, L.B.1
McGrogan, P.2
Flood, T.J.3
-
73
-
-
60749102218
-
Inflammatory bowel disease in CGD reproduces the clinicopathological features of Crohn's disease
-
Marks DJ, Miyagi K, Rahman FZ, et al. Inflammatory bowel disease in CGD reproduces the clinicopathological features of Crohn's disease. Am J Gastroenterol 2009;104:117-24.
-
(2009)
Am J Gastroenterol
, vol.104
, pp. 117-24
-
-
Marks, D.J.1
Miyagi, K.2
Rahman, F.Z.3
-
74
-
-
33947364434
-
Hepatic abnormalities in patients with chronic granulomatous disease
-
Hussain N, Feld JJ, Kleiner DE, et al. Hepatic abnormalities in patients with chronic granulomatous disease. Hepatology 2007;45: 675-83.
-
(2007)
Hepatology
, vol.45
, pp. 675-83
-
-
Hussain, N.1
Feld, J.J.2
Kleiner, D.E.3
-
75
-
-
0027937223
-
Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
-
Derry JM, Ochs HD, Francke U. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell 1994;78:635-44.
-
(1994)
Cell
, vol.78
, pp. 635-44
-
-
Derry, J.M.1
Ochs, H.D.2
Francke, U.3
-
76
-
-
0000788042
-
Familiarer angeborener Morbus Werlhofii?
-
Wiskott A. Familiarer, angeborener Morbus Werlhofii? Monatsschr Kiderheilkd 1937;68:212-6.
-
(1937)
Monatsschr Kiderheilkd
, vol.68
, pp. 212-6
-
-
Wiskott, A.1
-
77
-
-
0001102239
-
Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea
-
Aldrich RA, Steinberg AG, Campbell DC. Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. Pediatrics 1954;13: 133-9.
-
(1954)
Pediatrics
, vol.13
, pp. 133-9
-
-
Aldrich, R.A.1
Steinberg, A.G.2
Campbell, D.C.3
-
79
-
-
0018932524
-
The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979)
-
Perry GS 3rd, Spector BD, Schuman LM, et al. The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979). J Pediatr 1980;97:72-8.
-
(1980)
J Pediatr
, vol.97
, pp. 72-8
-
-
Spector, B.D.1
Schuman, L.M.2
-
80
-
-
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:e622-7.
-
(2003)
Pediatrics
, vol.111
-
-
Dupuis-Girod, S.1
Medioni, J.2
Haddad, E.3
-
81
-
-
0028116532
-
A multiinstitutional survey of the Wiskott-Aldrich syndrome
-
Sullivan KE, Mullen CA, Blaese RM, et al. A multiinstitutional survey of the Wiskott-Aldrich syndrome. J Pediatr 1994;125:876-85.
-
(1994)
J Pediatr
, vol.125
, pp. 876-85
-
-
Sullivan, K.E.1
Mullen, C.A.2
Blaese, R.M.3
-
82
-
-
0037385330
-
Foxp3 programs the development and function of CD4\+CD25\+ regulatory T cells
-
Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4\+CD25\+ regulatory T cells. Nat Immunol 2003;4:330-6.
-
(2003)
Nat Immunol
, vol.4
, pp. 330-6
-
-
Fontenot, J.D.1
Gavin, M.A.2
Rudensky, A.Y.3
-
83
-
-
0347785480
-
Control of regulatory T cell development by the transcription factor Foxp3
-
Hori S, Nomura T, Sakaguchi S. Control of regulatory T cell development by the transcription factor Foxp3. Science 2003;299:1057-61.
-
(2003)
Science
, vol.299
, pp. 1057-61
-
-
Hori, S.1
Nomura, T.2
Sakaguchi, S.3
-
84
-
-
0037385314
-
An essential role for Scurfin in CD4\+CD25\+ T regulatory cells
-
Khattri R, Cox T, Yasayko SA, et al. An essential role for Scurfin in CD4\+CD25\+ T regulatory cells. Nat Immunol 2003;4:337-42.
-
(2003)
Nat Immunol
, vol.4
, pp. 337-42
-
-
Khattri, R.1
Cox, T.2
Yasayko, S.A.3
-
85
-
-
0035813231
-
Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation
-
Schubert LA, Jeffery E, Zhang Y, et al. Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation. J Biol Chem 2001;276:37672-9.
-
(2001)
J Biol Chem
, vol.276
, pp. 37672-9
-
-
Schubert, L.A.1
Jeffery, E.2
Zhang, Y.3
-
86
-
-
0035167967
-
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
-
Bennett CL, Christie J, Ramsdell F, et al. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nat Genet 2001;27:20-1.
-
(2001)
Nat Genet
, vol.27
, pp. 20-1
-
-
Bennett, C.L.1
Christie, J.2
Ramsdell, F.3
-
87
-
-
0035163909
-
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
-
Wildin RS, Ramsdell F, Peake J, et al. X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy. Nat Genet 2001;27:18-20.
-
(2001)
Nat Genet
, vol.27
, pp. 18-20
-
-
Wildin, R.S.1
Ramsdell, F.2
Peake, J.3
-
88
-
-
0034526617
-
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome
-
Chatila TA, Blaeser F, Ho N, et al. JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome. J Clin Invest 2000;106:R75-81.
-
(2000)
J Clin Invest
, vol.106
-
-
Chatila, T.A.1
Blaeser, F.2
Ho, N.3
-
89
-
-
70350328995
-
FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome
-
D'Hennezel E, Ben-Shoshan M, Ochs HD, et al. FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome. N Engl J Med 2009;361:1710-3.
-
(2009)
N Engl J Med
, vol.361
, pp. 1710-3
-
-
D'Hennezel, E.1
Ben-Shoshan, M.2
Ochs, H.D.3
-
90
-
-
57249097253
-
Clinical and molecular profile of a new series of patients with immune dysregulation, poly-endocrinopathy, enteropathy, X-linked syndrome: Inconsistent correlation between forkhead box protein 3 expression and disease severity
-
Gambineri E, Perroni L, Passerini L, et al. Clinical and molecular profile of a new series of patients with immune dysregulation, poly-endocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity. J Allergy Clin Immunol 2008;122:1105.
-
(2008)
J Allergy Clin Immunol
, vol.122
, pp. 1105
-
-
Gambineri, E.1
Perroni, L.2
Passerini, L.3
-
91
-
-
0034723729
-
Manifestations and linkage analysis in X-linked autoimmunity- immunodeficiency syndrome
-
Ferguson PJ, Blanton SH, Saulsbury FT, et al. Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome. Am J Med Genet 2000;90:390-7.
-
(2000)
Am J Med Genet
, vol.90
, pp. 390-7
-
-
Ferguson, P.J.1
Blanton, S.H.2
Saulsbury, F.T.3
-
92
-
-
18244378309
-
Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)
-
Kobayashi I, Shiari R, Yamada M, et al. Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX). J Med Genet 2001;38: 874-6.
-
(2001)
J Med Genet
, vol.38
, pp. 874-6
-
-
Kobayashi, I.1
Shiari, R.2
Yamada, M.3
-
93
-
-
0020038580
-
An X-linked syndrome of diarrhea, polyendocrinopathy, and fatal infection in infancy
-
Powell BR, Buist NR, Stenzel P. An X-linked syndrome of diarrhea, polyendocrinopathy, and fatal infection in infancy. J Pediatr 1982;100: 731-7.
-
(1982)
J Pediatr
, vol.100
, pp. 731-7
-
-
Powell, B.R.1
Buist, N.R.2
Stenzel, P.3
-
94
-
-
33744976135
-
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) associated with pemphigoid nodularis: A case report and review of the literature
-
McGinness JL, Bivens MM, Greer KE, et al. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) associated with pemphigoid nodularis: a case report and review of the literature. J Am Acad Dermatol 2006;55:143-8.
-
(2006)
J Am Acad Dermatol
, vol.55
, pp. 143-8
-
-
McGinness, J.L.1
Bivens, M.M.2
Greer, K.E.3
-
95
-
-
44449126967
-
A remarkable depletion of both naive CD4\+ and CD8\+ with high proportion of memory T cells in an IPEX infant with a FOXP3 mutation in the forkhead domain
-
Costa-Carvalho BT, de Moraes-Pinto MI, de Almeida LC, et al. A remarkable depletion of both naive CD4\+ and CD8\+ with high proportion of memory T cells in an IPEX infant with a FOXP3 mutation in the forkhead domain. Scand J Immunol 2008;68:85-91.
-
(2008)
Scand J Immunol
, vol.68
, pp. 85-91
-
-
Costa-Carvalho, B.T.1
De Moraes-Pinto, M.I.2
De Almeida, L.C.3
-
96
-
-
0035053151
-
Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome
-
Levy-Lahad E, Wildin RS. Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: further evidence for an X-linked lethal syndrome. J Pediatr 2001;138:577-80.
-
(2001)
J Pediatr
, vol.138
, pp. 577-80
-
-
Levy-Lahad, E.1
Wildin, R.S.2
-
97
-
-
0029894371
-
X-linked immune dysregula-tion, neonatal insulin dependent diabetes, and intractable diarrhoea
-
Peake JE, McCrossin RB, Byrne G, et al. X-linked immune dysregula-tion, neonatal insulin dependent diabetes, and intractable diarrhoea. Arch Dis Child Fetal Neonatal Ed 1996;74:F195-9.
-
(1996)
Arch Dis Child Fetal Neonatal Ed
, vol.74
-
-
Peake, J.E.1
McCrossin, R.B.2
Byrne, G.3
-
98
-
-
30344482899
-
Clinical and molecular findings in IPEX syndrome
-
Myers AK, Perroni L, Costigan C, et al. Clinical and molecular findings in IPEX syndrome. Arch Dis Child 2006;91:63-4.
-
(2006)
Arch Dis Child
, vol.91
, pp. 63-4
-
-
Myers, A.K.1
Perroni, L.2
Costigan, C.3
-
99
-
-
0035821985
-
Treatment of the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) by allogeneic bone marrow transplantation
-
Baud O, Goulet O, Canioni D, et al. Treatment of the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) by allogeneic bone marrow transplantation. N Engl J Med 2001;344:1758-62.
-
(2001)
N Engl J Med
, vol.344
, pp. 1758-62
-
-
Baud, O.1
Goulet, O.2
Canioni, D.3
-
100
-
-
23944510233
-
Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, poly-endocrinopathy, enteropathy, X-linked syndrome)
-
Bindl L, Torgerson T, Perroni L, et al. Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, poly-endocrinopathy, enteropathy, X-linked syndrome). J Pediatr 2005;147: 256-9.
-
(2005)
J Pediatr
, vol.147
, pp. 256-9
-
-
Bindl, L.1
Torgerson, T.2
Perroni, L.3
-
101
-
-
3543045638
-
Prospective immunological profiling in a case of immune dysregulation, polyendocrinopathy, entero-pathy, X-linked syndrome (IPEX)
-
Bakke AC, Purtzer MZ, Wildin RS. Prospective immunological profiling in a case of immune dysregulation, polyendocrinopathy, entero-pathy, X-linked syndrome (IPEX). Clin Exp Immunol 2004;137:373-8.
-
(2004)
Clin Exp Immunol
, vol.137
, pp. 373-8
-
-
Bakke, A.C.1
Purtzer, M.Z.2
Wildin, R.S.3
-
102
-
-
11144355358
-
Dermatologic and im-munologic findings in the immune dysregulation, polyendocrino-pathy, enteropathy, X-linked syndrome
-
Nieves DS, Phipps RP, Pollock SJ, et al. Dermatologic and im-munologic findings in the immune dysregulation, polyendocrino-pathy, enteropathy, X-linked syndrome. Arch Dermatol 2004;140: 466-72.
-
(2004)
Arch Dermatol
, vol.140
, pp. 466-72
-
-
Nieves, D.S.1
Phipps, R.P.2
Pollock, S.J.3
-
103
-
-
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: 537-45.
-
(2002)
J Med Genet
, vol.39
, pp. 537-45
-
-
Wildin, R.S.1
Smyk-Pearson, S.2
Filipovich, A.H.3
-
104
-
-
70350507476
-
An infant with erythroderma, skin scaling, chronic emesis, and intractable diarrhea
-
Redding AR, Lew DB, Conley ME, et al. An infant with erythroderma, skin scaling, chronic emesis, and intractable diarrhea. Clin Pediatr (Phila) 2009;48:978-80.
-
(2009)
Clin Pediatr (Phila)
, vol.48
, pp. 978-80
-
-
Redding, A.R.1
Lew, D.B.2
Conley, M.E.3
-
105
-
-
34247862225
-
Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene
-
Torgerson TR, Linane A, Moes N, et al. Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene. Gastroenterology 2007;132:1705-17.
-
(2007)
Gastroenterology
, vol.132
, pp. 1705-17
-
-
Torgerson, T.R.1
Linane, A.2
Moes, N.3
-
107
-
-
55549134964
-
Manifestations and long-term outcome of food allergy in children after solid organ transplantation
-
Frischmeyer-Guerrerio PA, Wisniewski J, Wood RA, et al. Manifestations and long-term outcome of food allergy in children after solid organ transplantation. J Allergy Clin Immunol 2008;122:1031 e1-3.
-
(2008)
J Allergy Clin Immunol
, vol.122
-
-
Frischmeyer-Guerrerio, P.A.1
Wisniewski, J.2
Wood, R.A.3
|