-
1
-
-
0038593720
-
Parasitism and disease,
-
Princeton University Press
-
Smith T, (1934) Parasitism and disease, 196 Princeton University Press.
-
(1934)
, vol.196
-
-
Smith, T.1
-
2
-
-
33748993264
-
Global tuberculosis control. Surveillance, planning, financing
-
WHO, Geneva, WHO/HTM/TB/
-
WHO (2006) Global tuberculosis control. Surveillance, planning, financing. 2006 Geneva WHO/HTM/TB/.
-
(2006)
, vol.2006
-
-
-
3
-
-
29144484290
-
Tuberculosis in children and adults: two distinct genetic diseases
-
Alcais A, Fieschi C, Abel L, Casanova JL, (2005) Tuberculosis in children and adults: two distinct genetic diseases. J Exp Med 202: 1617-21.
-
(2005)
J Exp Med
, vol.202
, pp. 1617-1621
-
-
Alcais, A.1
Fieschi, C.2
Abel, L.3
Casanova, J.L.4
-
4
-
-
29144459487
-
Diagnose und Epidemiologie der Lungentuberculose des Kindes
-
Ranke K, (1910) Diagnose und Epidemiologie der Lungentuberculose des Kindes. Archiv fuer Kinderheilkunde 54: 279-306.
-
(1910)
Archiv Fuer Kinderheilkunde
, vol.54
, pp. 279-306
-
-
Ranke, K.1
-
5
-
-
84894653359
-
Frequency of tuberculosis in childhood
-
von Pirquet C, (1909) Frequency of tuberculosis in childhood. JAMA LII: 675-8.
-
(1909)
JAMA
, vol.LII
, pp. 675-678
-
-
von Pirquet, C.1
-
6
-
-
79954595211
-
A quantitative Modification of the von Pirquet tuberculin reaction and its value in diagnosis and prognosis
-
White WC, Graham DA, (1909) A quantitative Modification of the von Pirquet tuberculin reaction and its value in diagnosis and prognosis. J Med Res 20: 347-357.
-
(1909)
J Med Res
, vol.20
, pp. 347-357
-
-
White, W.C.1
Graham, D.A.2
-
7
-
-
0001776002
-
Tubercle bacilli in latent tuberculosis lesions and in lung tissue without tuberculous lesions
-
Opie EL, Arondon JD, (1927) Tubercle bacilli in latent tuberculosis lesions and in lung tissue without tuberculous lesions. Arch Pathol Lab Med 4: 1-21.
-
(1927)
Arch Pathol Lab Med
, vol.4
, pp. 1-21
-
-
Opie, E.L.1
Arondon, J.D.2
-
8
-
-
0036219062
-
Genetic dissection of immunity to mycobacteria: the human model
-
Casanova JL, Abel L, (2002) Genetic dissection of immunity to mycobacteria: the human model. Annu Rev Immunol 20: 581-620.
-
(2002)
Annu Rev Immunol
, vol.20
, pp. 581-620
-
-
Casanova, J.L.1
Abel, L.2
-
9
-
-
17044367835
-
Genetic susceptibility to tuberculosis
-
Bellamy R, (2005) Genetic susceptibility to tuberculosis. Clin Chest Med 26: 233-46.
-
(2005)
Clin Chest Med
, vol.26
, pp. 233-246
-
-
Bellamy, R.1
-
10
-
-
33846141491
-
Is susceptibility to tuberculosis acquired or inherited?
-
Schurr E, (2007) Is susceptibility to tuberculosis acquired or inherited? J Intern Med 261: 106-11.
-
(2007)
J Intern Med
, vol.261
, pp. 106-111
-
-
Schurr, E.1
-
11
-
-
77957020774
-
Life-threatening infectious diseases of childhood: single-gene inborn errors of immunity?
-
Alcais A, Quintana-Murci L, Thaler DS, Schurr E, Abel L, et al. (2010) Life-threatening infectious diseases of childhood: single-gene inborn errors of immunity? Ann N Y Acad Sci 1214: 18-33.
-
(2010)
Ann N Y Acad Sci
, vol.1214
, pp. 18-33
-
-
Alcais, A.1
Quintana-Murci, L.2
Thaler, D.S.3
Schurr, E.4
Abel, L.5
-
12
-
-
34547732069
-
Primary immunodeficiencies: a fields in its infancy
-
Casanova JL, Abel L, (2007) Primary immunodeficiencies: a fields in its infancy. Science 317: 617-619.
-
(2007)
Science
, vol.317
, pp. 617-619
-
-
Casanova, J.L.1
Abel, L.2
-
13
-
-
79954583215
-
Studies in atypical forms of tubercle bacilli isolated directly from the human tissues in cases of primary cervical adenitis: with special reference to the Theobald Smith glycerine bouillon reaction
-
Duval CW, (1909) Studies in atypical forms of tubercle bacilli isolated directly from the human tissues in cases of primary cervical adenitis: with special reference to the Theobald Smith glycerine bouillon reaction. J Exp Med 11: 403-429.
-
(1909)
J Exp Med
, vol.11
, pp. 403-429
-
-
Duval, C.W.1
-
15
-
-
0013655028
-
Familial susceptibility to tuberculosis; its importance as a public health problem
-
Vol5 Cambridge, MA Harvard University Press
-
Pfuffer R, (1944) Familial susceptibility to tuberculosis; its importance as a public health problem. Vol5 Cambridge, MA Harvard University Press.
-
(1944)
-
-
Pfuffer, R.1
-
16
-
-
79954596504
-
Tuberculotic twins; follow-up after 20 years
-
Von Verschuer OF, (1955) [Tuberculotic twins; follow-up after 20 years.]. Dtsch Med Wochenschr. 80: 1635-7.
-
(1955)
Dtsch Med Wochenschr
, vol.80
, pp. 1635-1637
-
-
von Verschuer, O.F.1
-
17
-
-
38449083851
-
Host genetics of mycobacterial diseases in mice and men: forward genetic studies of BCG-osis and tuberculosis
-
Fortin A, Abel L, Casanova JL, Gros P, (2007) Host genetics of mycobacterial diseases in mice and men: forward genetic studies of BCG-osis and tuberculosis. Annu Rev Genomics Hum Genet 8: 163-92.
-
(2007)
Annu Rev Genomics Hum Genet
, vol.8
, pp. 163-192
-
-
Fortin, A.1
Abel, L.2
Casanova, J.L.3
Gros, P.4
-
18
-
-
33745862748
-
An autosomal dominant major gene confers predisposition to pulmonary tuberculosis in adults
-
Baghdadi JE, Orlova M, Alter A, Ranque B, Chentoufi M, et al. (2006) An autosomal dominant major gene confers predisposition to pulmonary tuberculosis in adults. J Exp Med 203: 1679-84.
-
(2006)
J Exp Med
, vol.203
, pp. 1679-1684
-
-
Baghdadi, J.E.1
Orlova, M.2
Alter, A.3
Ranque, B.4
Chentoufi, M.5
-
19
-
-
73349135673
-
Two loci control tuberculin skin test reactivity in an area hyperendemic for tuberculosis
-
Cobat A, Gallant CJ, Simkin L, Black GF, Stanley K, et al. (2009) Two loci control tuberculin skin test reactivity in an area hyperendemic for tuberculosis. J Exp Med 206: 2583-91.
-
(2009)
J Exp Med
, vol.206
, pp. 2583-2591
-
-
Cobat, A.1
Gallant, C.J.2
Simkin, L.3
Black, G.F.4
Stanley, K.5
-
20
-
-
77956635151
-
Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2
-
Thye T, Vannberg FO, Wong SH, Owusu-Dabo E, Osei I, et al. (2010) Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. Nat Genet 42: 739-41.
-
(2010)
Nat Genet
, vol.42
, pp. 739-741
-
-
Thye, T.1
Vannberg, F.O.2
Wong, S.H.3
Owusu-Dabo, E.4
Osei, I.5
-
21
-
-
33749600724
-
Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features
-
Filipe-Santos O, Bustamante J, Chapgier A, Vogt G, de Beaucoudrey L, et al. (2006) Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features. Semin Immunol 18: 347-61.
-
(2006)
Semin Immunol
, vol.18
, pp. 347-361
-
-
Filipe-Santos, O.1
Bustamante, J.2
Chapgier, A.3
Vogt, G.4
de Beaucoudrey, L.5
-
22
-
-
49249138373
-
Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation
-
Vogt G, Bustamante J, Chapgier A, Feinberg J, Boisson-Dupuis S, et al. (2008) Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation. J Exp Med 205: 1729-37.
-
(2008)
J Exp Med
, vol.205
, pp. 1729-1737
-
-
Vogt, G.1
Bustamante, J.2
Chapgier, A.3
Feinberg, J.4
Boisson-Dupuis, S.5
-
23
-
-
79951647077
-
Germline but macrophage-tropic CYBB mutations in kindreds with X-linked prédisposition to tuberculous mycobacterial diseases
-
Bustamante J, Arias AA, Vogt G, Picard C, Blancas Galicia L, et al. (2011) Germline but macrophage-tropic CYBB mutations in kindreds with X-linked prédisposition to tuberculous mycobacterial diseases. Nat Immunol 12: 213-21.
-
(2011)
Nat Immunol
, vol.12
, pp. 213-221
-
-
Bustamante, J.1
Arias, A.A.2
Vogt, G.3
Picard, C.4
Blancas Galicia, L.5
-
24
-
-
79954593365
-
Mutations in IRF8 and human dendritic cells immunodeficiency
-
in press
-
Hambleton S, Salem S, Bustamante J, Bigley V, Boisson-Dupuis S, et al. Mutations in IRF8 and human dendritic cells immunodeficiency. N Engl J Med in press.
-
N Engl J Med
-
-
Hambleton, S.1
Salem, S.2
Bustamante, J.3
Bigley, V.4
Boisson-Dupuis, S.5
-
25
-
-
0035879825
-
Interleukin-12 receptor beta1 deficiency in a patient with abdominal tuberculosis
-
Altare F, Ensser A, Breiman A, Reichenbach J, Baghdadi JE, et al. (2001) Interleukin-12 receptor beta1 deficiency in a patient with abdominal tuberculosis. J Infect Dis 184: 231-6.
-
(2001)
J Infect Dis
, vol.184
, pp. 231-236
-
-
Altare, F.1
Ensser, A.2
Breiman, A.3
Reichenbach, J.4
Baghdadi, J.E.5
-
26
-
-
0038195718
-
Clinical tuberculosis in 2 of 3 siblings with interleukin-12 receptor beta1 deficiency
-
Caragol I, Raspall M, Fieschi C, Feinberg J, Larrosa MN, et al. (2003) Clinical tuberculosis in 2 of 3 siblings with interleukin-12 receptor beta1 deficiency. Clin Infect Dis 37: 302-6.
-
(2003)
Clin Infect Dis
, vol.37
, pp. 302-306
-
-
Caragol, I.1
Raspall, M.2
Fieschi, C.3
Feinberg, J.4
Larrosa, M.N.5
-
27
-
-
22944481430
-
Interleukin-12 receptor beta 1 chain deficiency in a child with disseminated tuberculosis
-
Ozbek N, Fieschi C, Yilmaz BT, de Beaucoudrey L, Demirhan B, et al. (2005) Interleukin-12 receptor beta 1 chain deficiency in a child with disseminated tuberculosis. Clin Infect Dis 40: e55-8.
-
(2005)
Clin Infect Dis
, vol.40
-
-
Ozbek, N.1
Fieschi, C.2
Yilmaz, B.T.3
de Beaucoudrey, L.4
Demirhan, B.5
-
28
-
-
0037450808
-
Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications
-
Fieschi C, Dupuis S, Catherinot E, Feinberg J, Bustamante J, et al. (2003) Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications. J Exp Med 197: 527-35.
-
(2003)
J Exp Med
, vol.197
, pp. 527-535
-
-
Fieschi, C.1
Dupuis, S.2
Catherinot, E.3
Feinberg, J.4
Bustamante, J.5
-
29
-
-
78649351360
-
Revisiting human IL12RB1 deficiency: a survey of 141 patients from 30 countries
-
De Beaucoudrey L, Samarina A, Bustamante J, Cobat A, Boisson-Dupuis S, et al. (2010) Revisiting human IL12RB1 deficiency: a survey of 141 patients from 30 countries. Medicine 89: 381-402.
-
(2010)
Medicine
, vol.89
, pp. 381-402
-
-
de Beaucoudrey, L.1
Samarina, A.2
Bustamante, J.3
Cobat, A.4
Boisson-Dupuis, S.5
-
30
-
-
34247172461
-
A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis
-
Sanal O, Turkkani G, Gumruk F, Yel L, Secmeer G, et al. (2007) A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis. Pediatr Infect Dis J 26: 366-8.
-
(2007)
Pediatr Infect Dis J
, vol.26
, pp. 366-368
-
-
Sanal, O.1
Turkkani, G.2
Gumruk, F.3
Yel, L.4
Secmeer, G.5
-
31
-
-
80555135404
-
Lethal tuberculosis in a previously healthy adult with IL-12 receptor deficiency
-
in press
-
Tabarsi P, Marjani M, Mansouri N, Farnia P, Boisson-Dupuis S, et al. Lethal tuberculosis in a previously healthy adult with IL-12 receptor deficiency. J Clin Immunol in press.
-
J Clin Immunol
-
-
Tabarsi, P.1
Marjani, M.2
Mansouri, N.3
Farnia, P.4
Boisson-Dupuis, S.5
-
32
-
-
0033694329
-
Treatment of infections in the patient with Mendelian susceptibility to mycobacterial infection
-
Holland SM, (2000) Treatment of infections in the patient with Mendelian susceptibility to mycobacterial infection. Microbes Infect 2: 1579-90.
-
(2000)
Microbes Infect
, vol.2
, pp. 1579-1590
-
-
Holland, S.M.1
-
33
-
-
79952223953
-
Treatment of disseminated mycobacterial infection with high dose IFN-g in a patient with IL-12Rb1 deficiency
-
Alangari AA, Al-Zamil F, Al-Mazrou A, Al-Muhsen S, Boisson-Dupuis S, et al. (2011) Treatment of disseminated mycobacterial infection with high dose IFN-g in a patient with IL-12Rb1 deficiency. Clin Dev Immunol 2011: 691956.
-
(2011)
Clin Dev Immunol
, vol.2011
, pp. 691956
-
-
Alangari, A.A.1
Al-Zamil, F.2
Al-Mazrou, A.3
Al-Muhsen, S.4
Boisson-Dupuis, S.5
-
34
-
-
0032948177
-
A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection
-
Jouanguy E, Lamhamedi-Cherradi S, Lammas D, Dorman SE, Fondanèche MC, et al. (1999) A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection. Nat Genet 21: 370-8.
-
(1999)
Nat Genet
, vol.21
, pp. 370-378
-
-
Jouanguy, E.1
Lamhamedi-Cherradi, S.2
Lammas, D.3
Dorman, S.E.4
Fondanèche, M.C.5
-
35
-
-
4644281630
-
A novel mutation in IFN-gamma receptor 2 with dominant negative activity: biological consequences of homozygous and heterozygous states
-
Rosenzweig SD, Dorman SE, Uzel G, Shaw S, Scurlock A, et al. (2004) A novel mutation in IFN-gamma receptor 2 with dominant negative activity: biological consequences of homozygous and heterozygous states. J Immunol 173: 4000-8.
-
(2004)
J Immunol
, vol.173
, pp. 4000-4008
-
-
Rosenzweig, S.D.1
Dorman, S.E.2
Uzel, G.3
Shaw, S.4
Scurlock, A.5
-
36
-
-
0035854542
-
Impairment of mycobacterial but not viral immunity by a germline human STAT1 mutation
-
Dupuis S, Dargemont C, Fieschi C, Thomassin N, Rosenzweig S, et al. (2001) Impairment of mycobacterial but not viral immunity by a germline human STAT1 mutation. Science 293: 300-3.
-
(2001)
Science
, vol.293
, pp. 300-303
-
-
Dupuis, S.1
Dargemont, C.2
Fieschi, C.3
Thomassin, N.4
Rosenzweig, S.5
-
37
-
-
34547123145
-
Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease
-
Chapgier A, Boisson-Dupuis S, Jouanguy E, Vogt G, Feinberg J, et al. (2006) Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease. PLoS Genet 2: e131.
-
(2006)
PLoS Genet
, vol.2
-
-
Chapgier, A.1
Boisson-Dupuis, S.2
Jouanguy, E.3
Vogt, G.4
Feinberg, J.5
-
38
-
-
73349110071
-
Exome sequencing identifies the cause of a Mendelian disorder
-
Ng SB, Buckingham KJ, Lee C, Bigham AW, Tabor HK, et al. (2010) Exome sequencing identifies the cause of a Mendelian disorder. Nat Genet 42: 30-5.
-
(2010)
Nat Genet
, vol.42
, pp. 30-35
-
-
Ng, S.B.1
Buckingham, K.J.2
Lee, C.3
Bigham, A.W.4
Tabor, H.K.5
-
39
-
-
78649772960
-
Whole-exome-sequencing-based discovery of human FADD deficiency
-
Bolze A, Byun M, McDonald D, Morgan NV, Abhyankar A, et al. (2010) Whole-exome-sequencing-based discovery of human FADD deficiency. Am J Hum Genet 87: 873-81.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 873-881
-
-
Bolze, A.1
Byun, M.2
McDonald, D.3
Morgan, N.V.4
Abhyankar, A.5
-
40
-
-
78149325696
-
Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma
-
Byun M, Abhyankar A, Lelarge V, Plancoulaine S, Palanduz A, et al. (2010) Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma. J Exp Med 207: 2307-12.
-
(2010)
J Exp Med
, vol.207
, pp. 2307-2312
-
-
Byun, M.1
Abhyankar, A.2
Lelarge, V.3
Plancoulaine, S.4
Palanduz, A.5
-
41
-
-
70350367182
-
Consanguinity and reproductive health among Arabs
-
Tadmouri GO, Nair P, Obeid T, Al Ali MT Al Khaja N, et al. (2009) Consanguinity and reproductive health among Arabs. Reproductive Health 6: 17.
-
(2009)
Reproductive Health
, vol.6
, pp. 17
-
-
Tadmouri, G.O.1
Nair, P.2
Obeid, T.3
Al Ali MT Al Khaja, N.4
-
42
-
-
0027944979
-
Consanguineous marriage in TUR and its impact on fertility
-
Tuncbilek E, Koc I, (2007) Consanguineous marriage in TUR and its impact on fertility. Ann Hum Genet 58: 321-9.
-
(2007)
Ann Hum Genet
, vol.58
, pp. 321-329
-
-
Tuncbilek, E.1
Koc, I.2
-
44
-
-
18244428735
-
Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency
-
Altare F, Durandy A, Lammas D, Emile JF, Lamhamedi S, et al. (1998) Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency. Science 280: 1432-5.
-
(1998)
Science
, vol.280
, pp. 1432-1435
-
-
Altare, F.1
Durandy, A.2
Lammas, D.3
Emile, J.F.4
Lamhamedi, S.5
|