-
1
-
-
0033952610
-
Epidemiology of HIV/AIDS in children
-
PID: 10697639, COI: 1:STN:280:DC%2BD3c7mt1OntQ%3D%3D
-
Lindegren ML, Steinberg S, Byers RH, Jr: Epidemiology of HIV/AIDS in children. Pediatr Clin North Am 2000, 47:1–20. DOI: 10.1016/S0031-3955(05)70192-9
-
(2000)
Pediatr Clin North Am
, vol.47
, pp. 1-20
-
-
Lindegren, M.L.1
Steinberg, S.2
Byers, R.H.3
-
2
-
-
0032963701
-
Human immunodeficiency virus infection associated arthritis: clinical characteristics
-
PID: 10332983, COI: 1:STN:280:DyaK1M3mtlOkug%3D%3D
-
Berman A, Cahn P, Perez H, et al.: Human immunodeficiency virus infection associated arthritis: clinical characteristics. J Rheumatol 1999, 26:1158–1162.
-
(1999)
J Rheumatol
, vol.26
, pp. 1158-1162
-
-
Berman, A.1
Cahn, P.2
Perez, H.3
-
3
-
-
0027760963
-
Rheumatic manifestations in human immunodeficiency virus positive and negative individuals: a study of 2 populations with similar risk factors
-
PID: 8308773, COI: 1:STN:280:ByuC2c7nvV0%3D
-
Medina-Rodriguez F, Guzman C, Jara LJ, et al.: Rheumatic manifestations in human immunodeficiency virus positive and negative individuals: a study of 2 populations with similar risk factors. J Rheumatol 1993, 20:1880–1884.
-
(1993)
J Rheumatol
, vol.20
, pp. 1880-1884
-
-
Medina-Rodriguez, F.1
Guzman, C.2
Jara, L.J.3
-
4
-
-
0029917640
-
Malignancies in pediatric AIDS
-
PID: 8680514, COI: 1:STN:280:BymB2M7ktF0%3D
-
Mueller BU, Pizzo PA: Malignancies in pediatric AIDS. Curr Opin Pediatr 1996, 8:45–49. DOI: 10.1097/00008480-199602000-00010
-
(1996)
Curr Opin Pediatr
, vol.8
, pp. 45-49
-
-
Mueller, B.U.1
Pizzo, P.A.2
-
5
-
-
0032146708
-
Genetic basis of abnormal B cell development
-
PID: 9722915, COI: 1:CAS:528:DyaK1cXlsFemt74%3D
-
Conley ME, Cooper MD: Genetic basis of abnormal B cell development. Curr Opin Immunol 1998, 10:399–406. DOI: 10.1016/S0952-7915(98)80112-X
-
(1998)
Curr Opin Immunol
, vol.10
, pp. 399-406
-
-
Conley, M.E.1
Cooper, M.D.2
-
6
-
-
0030475849
-
X-linked agammaglobulinemia: a clinical and molecular analysis
-
COI: 1:STN:280:ByiC3snnslQ%3D
-
Ochs HD, Smith CI: X-linked agammaglobulinemia: a clinical and molecular analysis. Medicine (Baltimore) 1996, 75:287–299. DOI: 10.1097/00005792-199611000-00001
-
(1996)
Medicine (Baltimore)
, vol.75
, pp. 287-299
-
-
Ochs, H.D.1
Smith, C.I.2
-
7
-
-
0030800175
-
Mycoplasmal arthritis in patients with primary immunoglobulin deficiency: clinical features and outcome in 18 patients
-
PID: 9236676, COI: 1:STN:280:ByiA2sboslM%3D
-
Franz A, Webster AD, Furr PM, Taylor-Robinson D: Mycoplasmal arthritis in patients with primary immunoglobulin deficiency: clinical features and outcome in 18 patients. Br J Rheumatol 1997, 36:661–668. DOI: 10.1093/rheumatology/36.6.661
-
(1997)
Br J Rheumatol
, vol.36
, pp. 661-668
-
-
Franz, A.1
Webster, A.D.2
Furr, P.M.3
Taylor-Robinson, D.4
-
8
-
-
0026769737
-
High- vs low-dose immunoglobulin therapy in the long-term treatment of X-linked agammaglobulinemia
-
PID: 1543181, COI: 1:STN:280:By2C1c%2FoslQ%3D
-
Liese JG, Wintergerst U, Tympner KD, Belohradsky BH: High- vs low-dose immunoglobulin therapy in the long-term treatment of X-linked agammaglobulinemia. Am J Dis Child 1992, 146:335–339.
-
(1992)
Am J Dis Child
, vol.146
, pp. 335-339
-
-
Liese, J.G.1
Wintergerst, U.2
Tympner, K.D.3
Belohradsky, B.H.4
-
9
-
-
0034525958
-
RT-nested PCR for the detection of enterovirus in biological samples from patients with suspected enteroviral infections
-
PID: 11149146, COI: 1:STN:280:DC%2BD3M%2Fpt1arsA%3D%3D
-
Palacios Poggio G, Cisterna D, Freire MC, Cello J: RT-nested PCR for the detection of enterovirus in biological samples from patients with suspected enteroviral infections. Rev Argent Microbiol 2000, 32:165–172.
-
(2000)
Rev Argent Microbiol
, vol.32
, pp. 165-172
-
-
Palacios Poggio, G.1
Cisterna, D.2
Freire, M.C.3
Cello, J.4
-
10
-
-
0035245212
-
Treatment of potentially lifethreatening enterovirus infections with pleconaril
-
PID: 11170912, COI: 1:CAS:528:DC%2BD3MXhtlGrsb4%3D
-
Rotbart HA, Webster AD: Treatment of potentially lifethreatening enterovirus infections with pleconaril. Clin Infect Dis 2001, 32:228–235. DOI: 10.1086/318452
-
(2001)
Clin Infect Dis
, vol.32
, pp. 228-235
-
-
Rotbart, H.A.1
Webster, A.D.2
-
11
-
-
0034264851
-
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)
-
PID: 11007475, COI: 1:CAS:528:DC%2BD3cXmsFWit7k%3D
-
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 2000, 102:565–575. DOI: 10.1016/S0092-8674(00)00079-9
-
(2000)
Cell
, vol.102
, pp. 565-575
-
-
Revy, P.1
Muto, T.2
Levy, Y.3
-
12
-
-
0029933493
-
Hyper-IgM syndrome associated with rheumatoid arthritis: report of RA in a patient with primary impaired CD40 pathway
-
PID: 8620305, COI: 1:STN:280:BymC1MvhvV0%3D
-
Sibilia J, Durandy A, Schaeverbeke T, Fermand JP:Hyper-IgM syndrome associated with rheumatoid arthritis: report of RA in a patient with primary impaired CD40 pathway. Br J Rheumatol 1996, 35:282–284. DOI: 10.1093/rheumatology/35.3.282
-
(1996)
Br J Rheumatol
, vol.35
, pp. 282-284
-
-
Sibilia, J.1
Durandy, A.2
Schaeverbeke, T.3
Fermand, J.P.4
-
13
-
-
0028033698
-
Clinical and immunologic studies of common variable immunodeficiency
-
PID: 7849813, COI: 1:STN:280:ByqC2M3msVA%3D
-
Cunningham-Rundles C:Clinical and immunologic studies of common variable immunodeficiency. Curr Opin Pediatr 1994, 6:676–681.
-
(1994)
Curr Opin Pediatr
, vol.6
, pp. 676-681
-
-
Cunningham-Rundles, C.1
-
14
-
-
0035832510
-
Primary immunodeficiency diseases: an experimental model for molecular medicine
-
PID: 11410213, COI: 1:STN:280:DC%2BD3MzkslOhtA%3D%3D, A review that outlines the information provided by the study of primary immunodeficiencies
-
Fischer A:Primary immunodeficiency diseases: an experimental model for molecular medicine. Lancet 2001, 357:1863–1869. A review that outlines the information provided by the study of primary immunodeficiencies. DOI: 10.1016/S0140-6736(00)04959-X
-
(2001)
Lancet
, vol.357
, pp. 1863-1869
-
-
Fischer, A.1
-
15
-
-
0034724857
-
Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease
-
PID: 10784449, COI: 1:CAS:528:DC%2BD3cXivFGhtbc%3D
-
Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, et al.: Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. Science 2000, 288:669–672. DOI: 10.1126/science.288.5466.669
-
(2000)
Science
, vol.288
, pp. 669-672
-
-
Cavazzana-Calvo, M.1
Hacein-Bey, S.2
de Saint Basile, G.3
-
16
-
-
0027398544
-
CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM
-
PID: 8094231, COI: 1:CAS:528:DyaK3sXhsVGqs7s%3D
-
DiSanto JP, Bonnefoy JY, Gauchat JF, et al.: CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM. Nature 1993, 361:541–543. DOI: 10.1038/361541a0
-
(1993)
Nature
, vol.361
, pp. 541-543
-
-
DiSanto, J.P.1
Bonnefoy, J.Y.2
Gauchat, J.F.3
-
17
-
-
0033498907
-
Enteroviral meningoencephalitis as a complication of X-linked hyper IgM syndrome
-
PID: 10228294, COI: 1:STN:280:DyaK1M3ks1Cjtg%3D%3D
-
Cunningham CK, Bonville CA, Ochs HD, et al.: Enteroviral meningoencephalitis as a complication of X-linked hyper IgM syndrome. J Pediatr 1999, 134:584–588. DOI: 10.1016/S0022-3476(99)70245-3
-
(1999)
J Pediatr
, vol.134
, pp. 584-588
-
-
Cunningham, C.K.1
Bonville, C.A.2
Ochs, H.D.3
-
18
-
-
0030702854
-
Clinical spectrum of X-linked hyper-IgM syndrome
-
PID: 9255191, COI: 1:STN:280:ByiA1Mbgs1Y%3D
-
Levy J, Espanol-Boren T, Thomas C, et al.: Clinical spectrum of X-linked hyper-IgM syndrome. J Pediatr 1997, 131:47–54. DOI: 10.1016/S0022-3476(97)70123-9
-
(1997)
J Pediatr
, vol.131
, pp. 47-54
-
-
Levy, J.1
Espanol-Boren, T.2
Thomas, C.3
-
19
-
-
0027446688
-
Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome
-
PID: 8229525, COI: 1:STN:280:ByuD2cnis1A%3D
-
Klein C, Lisowska-Grospierre B, LeDeist F, et al.: Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome. J Pediatr 1993, 123:921–928. DOI: 10.1016/S0022-3476(05)80388-9
-
(1993)
J Pediatr
, vol.123
, pp. 921-928
-
-
Klein, C.1
Lisowska-Grospierre, B.2
LeDeist, F.3
-
20
-
-
0027437515
-
Splenectomy and/or bone marrow transplantation in the management of the Wiskott-Aldrich syndrome: long-term follow-up of 62 cases
-
PID: 8219187, COI: 1:STN:280:ByuD3szltVA%3D
-
Mullen CA, Anderson KD, Blaese RM: Splenectomy and/or bone marrow transplantation in the management of the Wiskott-Aldrich syndrome: long-term follow-up of 62 cases. Blood 1993, 82:2961–2966.
-
(1993)
Blood
, vol.82
, pp. 2961-2966
-
-
Mullen, C.A.1
Anderson, K.D.2
Blaese, R.M.3
-
21
-
-
0031663617
-
ATM: from gene to function
-
PID: 9735376, COI: 1:CAS:528:DyaK1cXmsFWmu7c%3D
-
Rotman G, Shiloh Y: ATM: from gene to function. Hum Mol Genet 1998, 7:1555–1563. DOI: 10.1093/hmg/7.10.1555
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1555-1563
-
-
Rotman, G.1
Shiloh, Y.2
-
22
-
-
0036219062
-
Genetic dissection of immunity to mycobacteria: the human model
-
PID: 11861613, COI: 1:CAS:528:DC%2BD38XjtlWgtLc%3D, An extensive review of the spectrum of genetic conditions that may cause susceptibility to Bacille-Calmette Guèrin and environmental Mycobacterium or to more virulent Mycobacterium such as Mycobacterium tuberculosis or Mycobacterium leprae
-
Casanova JL, Abel L: Genetic dissection of immunity to mycobacteria: the human model. Annu Rev Immunol 2002, 20:581–620. An extensive review of the spectrum of genetic conditions that may cause susceptibility to Bacille-Calmette Guèrin and environmental Mycobacterium or to more virulent Mycobacterium such as Mycobacterium tuberculosis or Mycobacterium leprae. DOI: 10.1146/annurev.immunol.20.081501.125851
-
(2002)
Annu Rev Immunol
, vol.20
, pp. 581-620
-
-
Casanova, J.L.1
Abel, L.2
-
23
-
-
0028158262
-
Clinical consequences and treatment of primary immunodeficiency syndromes characterized by functional T and B lymphocyte anomalies (combined immune deficiency)
-
PID: 8121739, COI: 1:STN:280:ByuC28jhslM%3D
-
Berthet F, Le Deist F, Duliege AM, et al.:Clinical consequences and treatment of primary immunodeficiency syndromes characterized by functional T and B lymphocyte anomalies (combined immune deficiency). Pediatrics 1994, 93:265–270.
-
(1994)
Pediatrics
, vol.93
, pp. 265-270
-
-
Berthet, F.1
Le Deist, F.2
Duliege, A.M.3
-
24
-
-
0034057065
-
Autoimmune lymph oproliferative syndromes (ALPS): models for the study of peripheral tolerance
-
PID: 11324693, COI: 1:CAS:528:DC%2BD3cXhvFGjtrs%3D, Addresses the mechanisms and consequences of genetic diseases that have been recently recognized, and are characterized by with impaired lymphocyte death by apoptosis
-
Fischer A, Rieux-Laucat F, Le Deist F:Autoimmune lymph oproliferative syndromes (ALPS): models for the study of peripheral tolerance. Rev Immunogenet 2000, 2:52–60. Addresses the mechanisms and consequences of genetic diseases that have been recently recognized, and are characterized by with impaired lymphocyte death by apoptosis.
-
(2000)
Rev Immunogenet
, vol.2
, pp. 52-60
-
-
Fischer, A.1
Rieux-Laucat, F.2
Le Deist, F.3
-
25
-
-
0030583369
-
Clinical, immunological, and pathological consequences of Fas-deficient conditions
-
PID: 8806292
-
Le Deist F, Emile JF, Rieux-Laucat F, et al.: Clinical, immunological, and pathological consequences of Fas-deficient conditions. Lancet 1996, 348:719–723. DOI: 10.1016/S0140-6736(96)02293-3
-
(1996)
Lancet
, vol.348
, pp. 719-723
-
-
Le Deist, F.1
Emile, J.F.2
Rieux-Laucat, F.3
-
26
-
-
0033175907
-
Genetic basis of hemophagocytic lymphohistiocytosis syndrome
-
PID: 10402477, COI: 1:STN:280:DyaK1Mzjt1eitw%3D%3D
-
Dufourcq-Lagelouse R, Pastural E, Barrat FJ, et al.:Genetic basis of hemophagocytic lymphohistiocytosis syndrome. Int J Mol Med 1999, 4:127–133.
-
(1999)
Int J Mol Med
, vol.4
, pp. 127-133
-
-
Dufourcq-Lagelouse, R.1
Pastural, E.2
Barrat, F.J.3
-
27
-
-
0035479955
-
The role of cytotoxicity in lymphocyte homeostasis
-
PID: 11544002
-
de Saint Basile G, Fischer A: The role of cytotoxicity in lymphocyte homeostasis. Curr Opin Immunol 2001, 13:549–554. DOI: 10.1016/S0952-7915(00)00257-0
-
(2001)
Curr Opin Immunol
, vol.13
, pp. 549-554
-
-
de Saint Basile, G.1
Fischer, A.2
-
28
-
-
0035184142
-
Reactive haemophagocytic syndrome in children with inflammatory disorders: a retrospective study of 24 patients
-
PID: 11709613, COI: 1:STN:280:DC%2BD3MnnvFalsQ%3D%3D
-
Stephan JL, Kone-Paut I, Galambrun C, et al.: Reactive haemophagocytic syndrome in children with inflammatory disorders: a retrospective study of 24 patients. Rheumatology 2001, 40:1285–1292. DOI: 10.1093/rheumatology/40.11.1285
-
(2001)
Rheumatology
, vol.40
, pp. 1285-1292
-
-
Stephan, J.L.1
Kone-Paut, I.2
Galambrun, C.3
-
29
-
-
0033520970
-
Perforin gene defects in familial hemophagocytic lymphohistiocytosis
-
PID: 10583959, COI: 1:CAS:528:DyaK1MXnvFShsrg%3D
-
Stepp SE, Dufourcq-Lagelouse R, le Deist F, et al.:Perforin gene defects in familial hemophagocytic lymphohistiocytosis. Science 1999, 286:1957–1959. DOI: 10.1126/science.286.5446.1957
-
(1999)
Science
, vol.286
, pp. 1957-1959
-
-
Stepp, S.E.1
Dufourcq-Lagelouse, R.2
le Deist, F.3
-
30
-
-
0032190081
-
The X-linked lymphoproliferative- disease gene product SAP regulates signals induced through the co-receptor SLAM
-
PID: 9774102, COI: 1:CAS:528:DyaK1cXms1amsrg%3D
-
Sayos J, Wu C, Morra M, et al.:The X-linked lymphoproliferative- disease gene product SAP regulates signals induced through the co-receptor SLAM. Nature 1998, 395:462–469. DOI: 10.1038/26683
-
(1998)
Nature
, vol.395
, pp. 462-469
-
-
Sayos, J.1
Wu, C.2
Morra, M.3
-
31
-
-
0034307655
-
Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia
-
PID: 11001877, COI: 1:CAS:528:DC%2BD3cXntVartb0%3D
-
Dale DC, Person RE, Bolyard AA, et al.: Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 2000, 96:2317–2322.
-
(2000)
Blood
, vol.96
, pp. 2317-2322
-
-
Dale, D.C.1
Person, R.E.2
Bolyard, A.A.3
-
32
-
-
0034128751
-
Genetic, biochemical, and clinical features of chronic granulomatous disease
-
COI: 1:CAS:528:DC%2BD3cXktFGjt7s%3D
-
Segal BH, Leto TL, Gallin JI, et al.: Genetic, biochemical, and clinical features of chronic granulomatous disease. Medicine (Baltimore) 2000, 79:170–200. DOI: 10.1097/00005792-200005000-00004
-
(2000)
Medicine (Baltimore)
, vol.79
, pp. 170-200
-
-
Segal, B.H.1
Leto, T.L.2
Gallin, J.I.3
-
33
-
-
0034040532
-
Chronic granulomatous disease: report on a national registry of 368 patients
-
COI: 1:STN:280:DC%2BD3czgtlemtg%3D%3D
-
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. DOI: 10.1097/00005792-200005000-00003
-
(2000)
Medicine (Baltimore)
, vol.79
, pp. 155-169
-
-
Winkelstein, J.A.1
Marino, M.C.2
Johnston, R.B.3
-
34
-
-
0027988460
-
Long-term itraconazole prophylaxis against Aspergillus infections in thirty-two patients with chronic granulomatous disease
-
PID: 7996377, COI: 1:STN:280:ByqD1cfosVE%3D
-
Mouy R, Veber F, Blanche S, et al.: Long-term itraconazole prophylaxis against Aspergillus infections in thirty-two patients with chronic granulomatous disease. J Pediatr 1994, 125:998–1003. DOI: 10.1016/S0022-3476(05)82023-2
-
(1994)
J Pediatr
, vol.125
, pp. 998-1003
-
-
Mouy, R.1
Veber, F.2
Blanche, S.3
-
35
-
-
0033752720
-
Systemic lupus erythematosus, complement deficiency, and apoptosis
-
PID: 11079100, COI: 1:CAS:528:DC%2BD3cXosFSju7k%3D, These two reviews [35••,36••] address the role of complement inflammation and autoimmunity, and also susceptibility to infections Mark Walport’s review. Pickering’s review is almost exhaustive listing the complement disorders that may be associated with systemic lupus erythematosus and other inflammatory features humans and animals. It also discusses detail the hypothetical underlying mechanisms
-
Pickering MC, Botto M, Taylor PR, et al.:Systemic lupus erythematosus, complement deficiency, and apoptosis. Adv Immunol 2000, 76:227–324. These two reviews [35••,36••] address the role of complement in inflammation and autoimmunity, and also in susceptibility to infections in Mark Walport’s review. Pickering’s review is almost exhaustive in listing the complement disorders that may be associated with systemic lupus erythematosus and other inflammatory features in humans and animals. It also discusses in detail the hypothetical underlying mechanisms. DOI: 10.1016/S0065-2776(01)76021-X
-
(2000)
Adv Immunol
, vol.76
, pp. 227-324
-
-
Pickering, M.C.1
Botto, M.2
Taylor, P.R.3
-
36
-
-
0035849176
-
Complement: second of two parts
-
PID: 11297706, COI: 1:CAS:528:DC%2BD3MXjtFWgsbs%3D, These two reviews [35••,36••] address the role of complement inflammation and autoimmunity, and also susceptibility to infections Mark Walport’s review. Pickering’s review is almost exhaustive listing the complement disorders that may be associated with systemic lupus erythematosus and other inflammatory features humans and animals. It also discusses detail the hypothetical underlying mechanisms
-
Walport MJ:Complement: second of two parts. N Engl J Med 2001, 344:1140–1144. These two reviews [35••,36••] address the role of complement in inflammation and autoimmunity, and also in susceptibility to infections in Mark Walport’s review. Pickering’s review is almost exhaustive in listing the complement disorders that may be associated with systemic lupus erythematosus and other inflammatory features in humans and animals. It also discusses in detail the hypothetical underlying mechanisms. DOI: 10.1056/NEJM200104123441506
-
(2001)
N Engl J Med
, vol.344
, pp. 1140-1144
-
-
Walport, M.J.1
-
37
-
-
0033982375
-
Mannose binding lectin polymorphisms are associated with early age of disease onset and autoimmunity in common variable immunodeficiency
-
PID: 10652157, COI: 1:CAS:528:DC%2BD3cXhtlGnur8%3D
-
Mullighan CG, Marshall SE, Welsh KI: Mannose binding lectin polymorphisms are associated with early age of disease onset and autoimmunity in common variable immunodeficiency. Scand J Immunol 2000, 51:111–122. DOI: 10.1046/j.1365-3083.2000.00697.x
-
(2000)
Scand J Immunol
, vol.51
, pp. 111-122
-
-
Mullighan, C.G.1
Marshall, S.E.2
Welsh, K.I.3
-
38
-
-
0035949107
-
Deficiency of mannose-binding lectin and burden of infection in children with malignancy: a prospective study
-
PID: 11530147, COI: 1:CAS:528:DC%2BD3MXmt1yisr4%3D
-
Neth O, Hann I, Turner MW, Klein NJ: Deficiency of mannose-binding lectin and burden of infection in children with malignancy: a prospective study. Lancet 2001, 358:614–618. DOI: 10.1016/S0140-6736(01)05776-2
-
(2001)
Lancet
, vol.358
, pp. 614-618
-
-
Neth, O.1
Hann, I.2
Turner, M.W.3
Klein, N.J.4
-
39
-
-
0036499075
-
C1q deficiency and autoimmunity: the effects of genetic background on disease expression
-
PID: 11859149, COI: 1:CAS:528:DC%2BD38XhvVegtr8%3D
-
Mitchell DA, Pickering MC, Warren J, et al.: C1q deficiency and autoimmunity: the effects of genetic background on disease expression. J Immunol 2002, 168:2538–2543.
-
(2002)
J Immunol
, vol.168
, pp. 2538-2543
-
-
Mitchell, D.A.1
Pickering, M.C.2
Warren, J.3
-
40
-
-
0035856896
-
Hereditary periodic fever
-
PID: 11742050, COI: 1:CAS:528:DC%2BD3MXovFKjs7Y%3D, A comprehensive revue focusing on familial Mediterranean fever, hyper-IgD syndrome, and TNF-receptor-associated periodic syndrome
-
Drenth JP, van der Meer JW:Hereditary periodic fever. N Engl J Med 2001, 345:1748–1757. A comprehensive revue focusing on familial Mediterranean fever, hyper-IgD syndrome, and TNF-receptor-associated periodic syndrome. DOI: 10.1056/NEJMra010200
-
(2001)
N Engl J Med
, vol.345
, pp. 1748-1757
-
-
Drenth, J.P.1
van der Meer, J.W.2
-
41
-
-
0033515520
-
Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
-
PID: 10199409, COI: 1:CAS:528:DyaK1MXitlGmtLk%3D, The description of the molecular basis and the redefinition of a disease that may cause arthritis childhood
-
McDermott MF, Aksentijevich I, Galon J, et al.:Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 1999, 97:133–144. The description of the molecular basis and the redefinition of a disease that may cause arthritis in childhood. DOI: 10.1016/S0092-8674(00)80721-7
-
(1999)
Cell
, vol.97
, pp. 133-144
-
-
McDermott, M.F.1
Aksentijevich, I.2
Galon, J.3
-
42
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease
-
PID: 11385576, COI: 1:CAS:528:DC%2BD3MXksVShtLY%3D
-
Hugot JP, Chamaillard M, Zouali H, et al.:Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease. Nature 2001, 411:599–603. DOI: 10.1038/35079107
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
-
43
-
-
17944372335
-
CARD15 mutations in Blau syndrome
-
PID: 11528384, COI: 1:CAS:528:DC%2BD3MXmvFGmsrk%3D
-
Miceli-Richard C, Lesage S, Rybojad M, et al.: CARD15 mutations in Blau syndrome. Nat Genet 2001, 29:19–20. DOI: 10.1038/ng720
-
(2001)
Nat Genet
, vol.29
, pp. 19-20
-
-
Miceli-Richard, C.1
Lesage, S.2
Rybojad, M.3
-
44
-
-
0035179970
-
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold auto-inflammatory syndrome and Muckle-Wells syndrome
-
PID: 11687797, COI: 1:CAS:528:DC%2BD3MXotlWgs7Y%3D
-
Hoffman H, Mueller J, Broide D, et al.: Mutation of a new gene encoding a putative pyrin-like protein causes familial cold auto-inflammatory syndrome and Muckle-Wells syndrome. Nature Genet 2001, 29:301–305. DOI: 10.1038/ng756
-
(2001)
Nature Genet
, vol.29
, pp. 301-305
-
-
Hoffman, H.1
Mueller, J.2
Broide, D.3
-
45
-
-
0034906019
-
Autoimmunity and apoptosis: the Crohn’s connection
-
PID: 11485733, COI: 1:CAS:528:DC%2BD3MXlslSntrg%3D, An excellent review of the putative mechanisms by which molecules involved cell death pathways may cause inflammatory diseases such as Crohn’s disease or familial Mediterranean fever
-
Beutler B:Autoimmunity and apoptosis: the Crohn’s connection. Immunity 2001, 15:5–14. An excellent review of the putative mechanisms by which molecules involved in cell death pathways may cause inflammatory diseases such as Crohn’s disease or familial Mediterranean fever. DOI: 10.1016/S1074-7613(01)00176-5
-
(2001)
Immunity
, vol.15
, pp. 5-14
-
-
Beutler, B.1
-
46
-
-
0023894493
-
A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome: a specific entity analysed in 30 patients
-
PID: 3482735, COI: 1:STN:280:BieB3srot1E%3D
-
Prieur AM, Griscelli C, Lampert F, et al.:A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome: a specific entity analysed in 30 patients. Scand J Rheumatol Suppl 1987, 66:57–68.
-
(1987)
Scand J Rheumatol Suppl
, vol.66
, pp. 57-68
-
-
Prieur, A.M.1
Griscelli, C.2
Lampert, F.3
-
47
-
-
0036302235
-
Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes
-
PID: 12032915, COI: 1:CAS:528:DC%2BD38Xlt1Krtrs%3D
-
Feldmann J, Prieur AM, Quartier P, et al.: Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes. Am J Hum Genet 2002, 71:198–203. DOI: 10.1086/341357
-
(2002)
Am J Hum Genet
, vol.71
, pp. 198-203
-
-
Feldmann, J.1
Prieur, A.M.2
Quartier, P.3
-
48
-
-
0030870899
-
Syndromes and arthritis
-
PID: 9287384, COI: 1:STN:280:ByiH3szksVM%3D
-
Chalom EC, Ross J, Athreya BH: Syndromes and arthritis. Rheum Dis Clin North Am 1997, 23:709–727. DOI: 10.1016/S0889-857X(05)70354-9
-
(1997)
Rheum Dis Clin North Am
, vol.23
, pp. 709-727
-
-
Chalom, E.C.1
Ross, J.2
Athreya, B.H.3
-
49
-
-
0031720762
-
Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban, 1997
-
PID: 9779856, COI: 1:STN:280:DyaK1cvltFWgtA%3D%3D
-
Petty RE, Southwood TR, Baum J, et al.: Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban, 1997. J Rheumatol 1998, 25:1991–1994.
-
(1998)
J Rheumatol
, vol.25
, pp. 1991-1994
-
-
Petty, R.E.1
Southwood, T.R.2
Baum, J.3
-
50
-
-
0031783742
-
Juvenile arthritis: genetic update
-
PID: 9890094, COI: 1:STN:280:DyaK1M7gs1Olug%3D%3D
-
Albert ED, Scholz S:Juvenile arthritis: genetic update. Baillieres Clin Rheumatol 1998, 12:209–218. DOI: 10.1016/S0950-3579(98)80015-0
-
(1998)
Baillieres Clin Rheumatol
, vol.12
, pp. 209-218
-
-
Albert, E.D.1
Scholz, S.2
-
51
-
-
0032169769
-
A possible role for soluble IL-6 receptor in the pathogenesis of systemic onset juvenile chronic arthritis
-
PID: 9770335, COI: 1:CAS:528:DyaK1cXmslKitbw%3D
-
Keul R, Heinrich PC, Muller-Newen G, et al.: A possible role for soluble IL-6 receptor in the pathogenesis of systemic onset juvenile chronic arthritis. Cytokine 1998, 10:729–734. DOI: 10.1006/cyto.1997.0343
-
(1998)
Cytokine
, vol.10
, pp. 729-734
-
-
Keul, R.1
Heinrich, P.C.2
Muller-Newen, G.3
-
52
-
-
0033512202
-
Identification of a genetic risk factor for systemic juvenile rheumatoid arthritis in the 5’-flanking region of the TNFalpha gene and HLA genes
-
PID: 10616003, COI: 1:CAS:528:DC%2BD3cXjslansw%3D%3D
-
Date Y, Seki N, Kamizono S, et al.: Identification of a genetic risk factor for systemic juvenile rheumatoid arthritis in the 5’-flanking region of the TNFalpha gene and HLA genes. Arthritis Rheum 1999, 42:2577–2582. DOI: 10.1002/1529-0131(199912)42:12<2577::AID-ANR10>3.0.CO;2-O
-
(1999)
Arthritis Rheum
, vol.42
, pp. 2577-2582
-
-
Date, Y.1
Seki, N.2
Kamizono, S.3
-
53
-
-
0033659729
-
Cytokine polymorphisms and inflammation
-
PID: 11138346, COI: 1:STN:280:DC%2BD3M7ivFGktw%3D%3D
-
Woo P:Cytokine polymorphisms and inflammation. Clin Exp Rheumatol 2000, 18:767–771.
-
(2000)
Clin Exp Rheumatol
, vol.18
, pp. 767-771
-
-
Woo, P.1
-
54
-
-
0034986387
-
Hereditary predisposition to low interleukin-10 production in children with extended oligoarticular juvenile idiopathic arthritis
-
COI: 1:CAS:528:DC%2BD3MXkvFymu74%3D, A demonstration that the inheritance of IL-10 polymorphisms associated with low production of this anti-inflammatory cytokine is associated with a more severe outcome of oligoarticular-onset juvenile idiopathic arthritis, the most common form of noninfectious arthritis childhood. Preliminary experiments of gene therapy with IL-10 an animal model of arthritis have been published by the same team
-
Crawley E, Kon S, Woo P: Hereditary predisposition to low interleukin-10 production in children with extended oligoarticular juvenile idiopathic arthritis. Rheumatology (Oxford) 2001, 40:574–578. A demonstration that the inheritance of IL-10 polymorphisms associated with low production of this anti-inflammatory cytokine is associated with a more severe outcome of oligoarticular-onset juvenile idiopathic arthritis, the most common form of noninfectious arthritis in childhood. Preliminary experiments of gene therapy with IL-10 in an animal model of arthritis have been published by the same team. DOI: 10.1093/rheumatology/40.5.574
-
(2001)
Rheumatology (Oxford)
, vol.40
, pp. 574-578
-
-
Crawley, E.1
Kon, S.2
Woo, P.3
-
55
-
-
0028873394
-
A genetic association between juvenile rheumatoid arthritis and a novel interleukin- 1 alpha polymorphism
-
PID: 7848312, COI: 1:STN:280:ByqC2M7gsFQ%3D
-
McDowell TL, Symons JA, Ploski R, et al.:A genetic association between juvenile rheumatoid arthritis and a novel interleukin- 1 alpha polymorphism. Arthritis Rheum 1995, 38:221–228. DOI: 10.1002/art.1780380210
-
(1995)
Arthritis Rheum
, vol.38
, pp. 221-228
-
-
McDowell, T.L.1
Symons, J.A.2
Ploski, R.3
-
56
-
-
0033851492
-
Selective recruitment of polarized T cells expressing CCR5 and CXCR3 to the inflamed joints of children with juvenile idiopathic arthritis
-
PID: 10765921, COI: 1:CAS:528:DC%2BD3cXivFOitr4%3D
-
Wedderburn LR, Robinson N, Patel A, et al.:Selective recruitment of polarized T cells expressing CCR5 and CXCR3 to the inflamed joints of children with juvenile idiopathic arthritis. Arthritis Rheum 2000, 43:765–774. DOI: 10.1002/1529-0131(200004)43:4<765::AID-ANR7>3.0.CO;2-B
-
(2000)
Arthritis Rheum
, vol.43
, pp. 765-774
-
-
Wedderburn, L.R.1
Robinson, N.2
Patel, A.3
-
57
-
-
0036230130
-
How antibodies to a ubiquitous cytoplasmic enzyme may provoke jointspecific autoimmune disease
-
PID: 11896391, COI: 1:CAS:528:DC%2BD38Xis1Kksbk%3D, This paper shows the most recent findings of Mathys and Benoist’s team with a mouse model of rheumatoid arthritis. These authors previously shown that arthritis the K/BxN mouse model results from pathogenic immunoglobulins that recognize an ubiquitous glycolytic enzyme, glucose-6-phosphate isomerase (GPI), and that a functional alternative complement pathway was required for disease expression. They here show by immunohistology extracellular accumulation of GPI on the lining of the articular cavity normal mice and that these GPI deposits are amplified and localized with IgG and C3 complement arthritic mice and humans with rheumatoid arthritis. Their hypothesis is that the expression of the disease on the cartilage is because of the absence of cellular inhibitors of the alternative pathway at this level. These findings are favor of a model which adaptive and innate immunity interact causing arthritis
-
Matsumoto I, Maccioni M, Lee DM, et al.:How antibodies to a ubiquitous cytoplasmic enzyme may provoke jointspecific autoimmune disease. Nat Immunol 2002, 3:360–365. This paper shows the most recent findings of Mathys and Benoist’s team with a mouse model of rheumatoid arthritis. These authors previously shown that arthritis in the K/BxN mouse model results from pathogenic immunoglobulins that recognize an ubiquitous glycolytic enzyme, glucose-6-phosphate isomerase (GPI), and that a functional alternative complement pathway was required for disease expression. They here show by immunohistology extracellular accumulation of GPI on the lining of the articular cavity in normal mice and that these GPI deposits are amplified and localized with IgG and C3 complement in arthritic mice and in humans with rheumatoid arthritis. Their hypothesis is that the expression of the disease on the cartilage is because of the absence of cellular inhibitors of the alternative pathway at this level. These findings are in favor of a model in which adaptive and innate immunity interact in causing arthritis. DOI: 10.1038/ni772
-
(2002)
Nat Immunol
, vol.3
, pp. 360-365
-
-
Matsumoto, I.1
Maccioni, M.2
Lee, D.M.3
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