-
1
-
-
34547732069
-
Primary immunodeficiencies: a field in its infancy
-
Casanova J.L., and Abel L. Primary immunodeficiencies: a field in its infancy. Science 317 (2007) 617-619
-
(2007)
Science
, vol.317
, pp. 617-619
-
-
Casanova, J.L.1
Abel, L.2
-
2
-
-
68049116664
-
Recent advances in primary immunodeficiencies: identification of novel genetic defects and unanticipated phenotypes
-
Jan 28 [Epub ahead of print]
-
Pessach I., Walter J., and Notarangelo L.D. Recent advances in primary immunodeficiencies: identification of novel genetic defects and unanticipated phenotypes. Pediatr Res (2009) Jan 28 [Epub ahead of print]
-
(2009)
Pediatr Res
-
-
Pessach, I.1
Walter, J.2
Notarangelo, L.D.3
-
3
-
-
34948872289
-
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
-
Geha R.S., Notarangelo L.D., Casanova J.L., Chapel H., Conley M.E., Fischer A., Hammarstrom L., Nonoyama S., Ochs H.D., Puck J.M., et al. Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee. J Allergy Clin Immunol 120 (2007) 776-794
-
(2007)
J Allergy Clin Immunol
, vol.120
, pp. 776-794
-
-
Geha, R.S.1
Notarangelo, L.D.2
Casanova, J.L.3
Chapel, H.4
Conley, M.E.5
Fischer, A.6
Hammarstrom, L.7
Nonoyama, S.8
Ochs, H.D.9
Puck, J.M.10
-
4
-
-
0000419304
-
Agammaglobulinemia
-
Bruton O.C. Agammaglobulinemia. Pediatrics 9 (1952) 722-728
-
(1952)
Pediatrics
, vol.9
, pp. 722-728
-
-
Bruton, O.C.1
-
5
-
-
67650744339
-
Primary B cell immunodeficiencies: comparisons and contrasts
-
Conley M.E., Dobbs A.K., Farmer D.M., Kilic S., Paris K., Grigoriadou S., Coustan-Smith E., Howard V., and Campana D. Primary B cell immunodeficiencies: comparisons and contrasts. Annu Rev Immunol 27 (2009) 199-227
-
(2009)
Annu Rev Immunol
, vol.27
, pp. 199-227
-
-
Conley, M.E.1
Dobbs, A.K.2
Farmer, D.M.3
Kilic, S.4
Paris, K.5
Grigoriadou, S.6
Coustan-Smith, E.7
Howard, V.8
Campana, D.9
-
6
-
-
70349741029
-
Genetics of hypogammaglobulinemia: what do we really know?
-
Conley M.E. Genetics of hypogammaglobulinemia: what do we really know?. Curr Opin Immunol 21 (2009) 466-471
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 466-471
-
-
Conley, M.E.1
-
7
-
-
77049235105
-
Infantile genetic agranulocytosis
-
Kostmann R. Infantile genetic agranulocytosis. Acta Pediatr Scand 45 (1956) 1-78
-
(1956)
Acta Pediatr Scand
, vol.45
, pp. 1-78
-
-
Kostmann, R.1
-
8
-
-
70349747024
-
Novel genetic etiologies of severe congenital neutropenia
-
Klein C. Novel genetic etiologies of severe congenital neutropenia. Curr Opin Immunol 21 (2009) 472-480
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 472-480
-
-
Klein, C.1
-
9
-
-
0019195556
-
Neutropenia and impaired neutrophil migration in type IB glycogen storage disease
-
Beaudet A.L., Anderson D.C., Michels V.V., Arion W.J., and Lange A.J. Neutropenia and impaired neutrophil migration in type IB glycogen storage disease. J Pediatr 97 (1980) 906-910
-
(1980)
J Pediatr
, vol.97
, pp. 906-910
-
-
Beaudet, A.L.1
Anderson, D.C.2
Michels, V.V.3
Arion, W.J.4
Lange, A.J.5
-
10
-
-
58249089770
-
A syndrome with congenital neutropenia and mutations in G6PC3
-
Boztug K., Appaswamy G., Ashikov A., Schaffer A.A., Salzer U., Diestelhorst J., Germeshausen M., Brandes G., Lee-Gossler J., Noyan F., et al. A syndrome with congenital neutropenia and mutations in G6PC3. N Engl J Med 360 (2009) 32-43
-
(2009)
N Engl J Med
, vol.360
, pp. 32-43
-
-
Boztug, K.1
Appaswamy, G.2
Ashikov, A.3
Schaffer, A.A.4
Salzer, U.5
Diestelhorst, J.6
Germeshausen, M.7
Brandes, G.8
Lee-Gossler, J.9
Noyan, F.10
-
11
-
-
33845904894
-
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
-
Klein C., Grudzien M., Appaswamy G., Germeshausen M., Sandrock I., Schaffer A.A., Rathinam C., Boztug K., Schwinzer B., Rezaei N., et al. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet 39 (2007) 86-92
-
(2007)
Nat Genet
, vol.39
, pp. 86-92
-
-
Klein, C.1
Grudzien, M.2
Appaswamy, G.3
Germeshausen, M.4
Sandrock, I.5
Schaffer, A.A.6
Rathinam, C.7
Boztug, K.8
Schwinzer, B.9
Rezaei, N.10
-
12
-
-
42049117271
-
Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations
-
Germeshausen M., Grudzien M., Zeidler C., Abdollahpour H., Yetgin S., Rezaei N., Ballmaier M., Grimbacher B., Welte K., and Klein C. Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations. Blood 111 (2008) 4954-4957
-
(2008)
Blood
, vol.111
, pp. 4954-4957
-
-
Germeshausen, M.1
Grudzien, M.2
Zeidler, C.3
Abdollahpour, H.4
Yetgin, S.5
Rezaei, N.6
Ballmaier, M.7
Grimbacher, B.8
Welte, K.9
Klein, C.10
-
13
-
-
51649124219
-
Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations
-
Carlsson G., van't Hooft I., Melin M., Entesarian M., Laurencikas E., Nennesmo I., Trebinska A., Grzybowska E., Palmblad J., Dahl N., et al. Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations. J Intern Med 264 (2008) 388-400
-
(2008)
J Intern Med
, vol.264
, pp. 388-400
-
-
Carlsson, G.1
van't Hooft, I.2
Melin, M.3
Entesarian, M.4
Laurencikas, E.5
Nennesmo, I.6
Trebinska, A.7
Grzybowska, E.8
Palmblad, J.9
Dahl, N.10
-
14
-
-
70349754453
-
Genetic etiologies of leucocyte adhesion defects
-
Etzioni A. Genetic etiologies of leucocyte adhesion defects. Curr Opin Immunol 21 (2009) 481-486
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 481-486
-
-
Etzioni, A.1
-
15
-
-
0141670816
-
LAD-III, a novel group of leukocyte integrin activation deficiencies
-
Alon R., and Etzioni A. LAD-III, a novel group of leukocyte integrin activation deficiencies. Trends Immunol 24 (2003) 561-566
-
(2003)
Trends Immunol
, vol.24
, pp. 561-566
-
-
Alon, R.1
Etzioni, A.2
-
16
-
-
34147154889
-
Natural history and early diagnosis of LAD-1/variant syndrome
-
Kuijpers T.W., van Bruggen R., Kamerbeek N., Tool A.T., Hicsonmez G., Gurgey A., Karow A., Verhoeven A.J., Seeger K., Sanal O., et al. Natural history and early diagnosis of LAD-1/variant syndrome. Blood 109 (2007) 3529-3537
-
(2007)
Blood
, vol.109
, pp. 3529-3537
-
-
Kuijpers, T.W.1
van Bruggen, R.2
Kamerbeek, N.3
Tool, A.T.4
Hicsonmez, G.5
Gurgey, A.6
Karow, A.7
Verhoeven, A.J.8
Seeger, K.9
Sanal, O.10
-
17
-
-
34447255182
-
A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets
-
Pasvolsky R., Feigelson S.W., Kilic S.S., Simon A.J., Tal-Lapidot G., Grabovsky V., Crittenden J.R., Amariglio N., Safran M., Graybiel A.M., et al. A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets. J Exp Med 204 (2007) 1571-1582
-
(2007)
J Exp Med
, vol.204
, pp. 1571-1582
-
-
Pasvolsky, R.1
Feigelson, S.W.2
Kilic, S.S.3
Simon, A.J.4
Tal-Lapidot, G.5
Grabovsky, V.6
Crittenden, J.R.7
Amariglio, N.8
Safran, M.9
Graybiel, A.M.10
-
18
-
-
55249083592
-
Kindlin-3: a new gene involved in the pathogenesis of LAD-III
-
Mory A., Feigelson S.W., Yarali N., Kilic S.S., Bayhan G.I., Gershoni-Baruch R., Etzioni A., and Alon R. Kindlin-3: a new gene involved in the pathogenesis of LAD-III. Blood 112 (2008) 2591
-
(2008)
Blood
, vol.112
, pp. 2591
-
-
Mory, A.1
Feigelson, S.W.2
Yarali, N.3
Kilic, S.S.4
Bayhan, G.I.5
Gershoni-Baruch, R.6
Etzioni, A.7
Alon, R.8
-
19
-
-
66549121768
-
LAD-1/variant syndrome is caused by mutations in FERMT3
-
Kuijpers T.W., van de Vijver E., Weterman M.A., de Boer M., Tool A.T., van den Berg T.K., Moser M., Jakobs M.E., Seeger K., Sanal O., et al. LAD-1/variant syndrome is caused by mutations in FERMT3. Blood 113 (2009) 4740-4746
-
(2009)
Blood
, vol.113
, pp. 4740-4746
-
-
Kuijpers, T.W.1
van de Vijver, E.2
Weterman, M.A.3
de Boer, M.4
Tool, A.T.5
van den Berg, T.K.6
Moser, M.7
Jakobs, M.E.8
Seeger, K.9
Sanal, O.10
-
20
-
-
61949240364
-
A point mutation in KINDLIN3 ablates activation of three integrin subfamilies in humans
-
Malinin N.L., Zhang L., Choi J., Ciocea A., Razorenova O., Ma Y.Q., Podrez E.A., Tosi M., Lennon D.P., Caplan A.I., et al. A point mutation in KINDLIN3 ablates activation of three integrin subfamilies in humans. Nat Med 15 (2009) 313-318
-
(2009)
Nat Med
, vol.15
, pp. 313-318
-
-
Malinin, N.L.1
Zhang, L.2
Choi, J.3
Ciocea, A.4
Razorenova, O.5
Ma, Y.Q.6
Podrez, E.A.7
Tosi, M.8
Lennon, D.P.9
Caplan, A.I.10
-
21
-
-
61949086409
-
Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation
-
Svensson L., Howarth K., McDowall A., Patzak I., Evans R., Ussar S., Moser M., Metin A., Fried M., Tomlinson I., et al. Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation. Nat Med 15 (2009) 306-312
-
(2009)
Nat Med
, vol.15
, pp. 306-312
-
-
Svensson, L.1
Howarth, K.2
McDowall, A.3
Patzak, I.4
Evans, R.5
Ussar, S.6
Moser, M.7
Metin, A.8
Fried, M.9
Tomlinson, I.10
-
22
-
-
0014008065
-
Job's syndrome. Recurrent, "cold", staphylococcal abscesses
-
Davis S.D., Schaller J., and Wedgwood R.J. Job's syndrome. Recurrent, "cold", staphylococcal abscesses. Lancet 1 (1966) 1013-1015
-
(1966)
Lancet
, vol.1
, pp. 1013-1015
-
-
Davis, S.D.1
Schaller, J.2
Wedgwood, R.J.3
-
23
-
-
0015266954
-
Extreme hyperimmunoglobulinemia E and undue susceptibility to infection
-
Buckley R.H., Wray B.B., and Belmaker E.Z. Extreme hyperimmunoglobulinemia E and undue susceptibility to infection. Pediatrics 49 (1972) 59-70
-
(1972)
Pediatrics
, vol.49
, pp. 59-70
-
-
Buckley, R.H.1
Wray, B.B.2
Belmaker, E.Z.3
-
24
-
-
34548317417
-
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
-
Minegishi Y., Saito M., Tsuchiya S., Tsuge I., Takada H., Hara T., Kawamura N., Ariga T., Pasic S., Stojkovic O., et al. Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature 448 (2007) 1058-1062
-
(2007)
Nature
, vol.448
, pp. 1058-1062
-
-
Minegishi, Y.1
Saito, M.2
Tsuchiya, S.3
Tsuge, I.4
Takada, H.5
Hara, T.6
Kawamura, N.7
Ariga, T.8
Pasic, S.9
Stojkovic, O.10
-
25
-
-
33845897463
-
Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity
-
Minegishi Y., Saito M., Morio T., Watanabe K., Agematsu K., Tsuchiya S., Takada H., Hara T., Kawamura N., Ariga T., et al. Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity. Immunity 25 (2006) 745-755
-
(2006)
Immunity
, vol.25
, pp. 745-755
-
-
Minegishi, Y.1
Saito, M.2
Morio, T.3
Watanabe, K.4
Agematsu, K.5
Tsuchiya, S.6
Takada, H.7
Hara, T.8
Kawamura, N.9
Ariga, T.10
-
26
-
-
35348960378
-
STAT3 mutations in the Hyper-IgE syndrome
-
Holland S.M., Deleo F.R., Elloumi H.Z., Hsu A.P., Uzel G., Brodsky N., Freeman A.F., Demidowich A., Davis J., Turner M.L., et al. STAT3 mutations in the Hyper-IgE syndrome. N Engl J Med 357 (2007) 1608-1619
-
(2007)
N Engl J Med
, vol.357
, pp. 1608-1619
-
-
Holland, S.M.1
Deleo, F.R.2
Elloumi, H.Z.3
Hsu, A.P.4
Uzel, G.5
Brodsky, N.6
Freeman, A.F.7
Demidowich, A.8
Davis, J.9
Turner, M.L.10
-
27
-
-
46949086109
-
Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells
-
de Beaucoudrey L., Puel A., Filipe-Santos O., Cobat A., Ghandil P., Chrabieh M., Feinberg J., von Bernuth H., Samarina A., Janniere L., et al. Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells. J Exp Med 205 (2008) 1543-1550
-
(2008)
J Exp Med
, vol.205
, pp. 1543-1550
-
-
de Beaucoudrey, L.1
Puel, A.2
Filipe-Santos, O.3
Cobat, A.4
Ghandil, P.5
Chrabieh, M.6
Feinberg, J.7
von Bernuth, H.8
Samarina, A.9
Janniere, L.10
-
28
-
-
46949089128
-
Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3
-
Ma C.S., Chew G.Y., Simpson N., Priyadarshi A., Wong M., Grimbacher B., Fulcher D.A., Tangye S.G., and Cook M.C. Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3. J Exp Med 205 (2008) 1551-1557
-
(2008)
J Exp Med
, vol.205
, pp. 1551-1557
-
-
Ma, C.S.1
Chew, G.Y.2
Simpson, N.3
Priyadarshi, A.4
Wong, M.5
Grimbacher, B.6
Fulcher, D.A.7
Tangye, S.G.8
Cook, M.C.9
-
29
-
-
41449110468
-
Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
-
Milner J.D., Brenchley J.M., Laurence A., Freeman A.F., Hill B.J., Elias K.M., Kanno Y., Spalding C., Elloumi H.Z., Paulson M.L., et al. Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome. Nature 452 (2008) 773-776
-
(2008)
Nature
, vol.452
, pp. 773-776
-
-
Milner, J.D.1
Brenchley, J.M.2
Laurence, A.3
Freeman, A.F.4
Hill, B.J.5
Elias, K.M.6
Kanno, Y.7
Spalding, C.8
Elloumi, H.Z.9
Paulson, M.L.10
-
30
-
-
67449149963
-
Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome
-
Minegishi Y., Saito M., Nagasawa M., Takada H., Hara T., Tsuchiya S., Agematsu K., Yamada M., Kawamura N., Ariga T., et al. Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome. J Exp Med 206 (2009) 1291-1301
-
(2009)
J Exp Med
, vol.206
, pp. 1291-1301
-
-
Minegishi, Y.1
Saito, M.2
Nagasawa, M.3
Takada, H.4
Hara, T.5
Tsuchiya, S.6
Agematsu, K.7
Yamada, M.8
Kawamura, N.9
Ariga, T.10
-
31
-
-
70349751667
-
Vanhollebeke B: Human innate immunity against African trypanosomes
-
Pays E. Vanhollebeke B: Human innate immunity against African trypanosomes. Curr Opin Immunol 21 (2009) 493-498
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 493-498
-
-
Pays, E.1
-
32
-
-
33845868544
-
Human Trypanosoma evansi infection linked to a lack of apolipoprotein L-I
-
Vanhollebeke B., Truc P., Poelvoorde P., Pays A., Joshi P.P., Katti R., Jannin J.G., and Pays E. Human Trypanosoma evansi infection linked to a lack of apolipoprotein L-I. N Engl J Med 355 (2006) 2752-2756
-
(2006)
N Engl J Med
, vol.355
, pp. 2752-2756
-
-
Vanhollebeke, B.1
Truc, P.2
Poelvoorde, P.3
Pays, A.4
Joshi, P.P.5
Katti, R.6
Jannin, J.G.7
Pays, E.8
-
33
-
-
77049164783
-
Protection afforded by sickle cell trait against subtertian malarian infection
-
Allison A.C. Protection afforded by sickle cell trait against subtertian malarian infection. Br Med J 1 (1954) 290-294
-
(1954)
Br Med J
, vol.1
, pp. 290-294
-
-
Allison, A.C.1
-
34
-
-
22544441601
-
How malaria has affected the human genome and what human genetics can teach us about malaria
-
Kwiatkowski D.P. How malaria has affected the human genome and what human genetics can teach us about malaria. Am J Hum Genet 77 (2005) 171-192
-
(2005)
Am J Hum Genet
, vol.77
, pp. 171-192
-
-
Kwiatkowski, D.P.1
-
35
-
-
67349278465
-
Genome-wide and fine-resolution association analysis of malaria in West Africa
-
May 24 [Epub ahead of print]
-
Jallow M., Teo Y.Y., Small K.S., Rockett K.A., Deloukas P., Clark T.G., Kivinen K., Bojang K.A., Conway D.J., Pinder M., et al. Genome-wide and fine-resolution association analysis of malaria in West Africa. Nat Genet (2009) May 24 [Epub ahead of print]
-
(2009)
Nat Genet
-
-
Jallow, M.1
Teo, Y.Y.2
Small, K.S.3
Rockett, K.A.4
Deloukas, P.5
Clark, T.G.6
Kivinen, K.7
Bojang, K.A.8
Conway, D.J.9
Pinder, M.10
-
36
-
-
70349756907
-
Genetic control of innate immunity to malaria
-
Allison A.C. Genetic control of innate immunity to malaria. Curr Opin Immunol 21 (2009) 499-505
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 499-505
-
-
Allison, A.C.1
-
37
-
-
42049086504
-
Hemophagocytic lymphohistiocytosis and other hemophagocytic disorders
-
viii
-
Filipovich A.H. Hemophagocytic lymphohistiocytosis and other hemophagocytic disorders. Immunol Allergy Clin North Am 28 (2008) 293-313 viii
-
(2008)
Immunol Allergy Clin North Am
, vol.28
, pp. 293-313
-
-
Filipovich, A.H.1
-
38
-
-
35548967700
-
Complement regulatory genes and hemolytic uremic syndromes
-
Kavanagh D., Richards A., and Atkinson J. Complement regulatory genes and hemolytic uremic syndromes. Annu Rev Med 59 (2008) 293-309
-
(2008)
Annu Rev Med
, vol.59
, pp. 293-309
-
-
Kavanagh, D.1
Richards, A.2
Atkinson, J.3
-
39
-
-
70349756909
-
The immunopathogenesis of Crohn's disease: a three stage model
-
Sewell G.W., Marks D.J., and Segal A.W. The immunopathogenesis of Crohn's disease: a three stage model. Curr Opin Immunol 21 (2009) 506-513
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 506-513
-
-
Sewell, G.W.1
Marks, D.J.2
Segal, A.W.3
-
40
-
-
69449105914
-
Disordered macrophage cytokine secretion underlies impaired acute inflammation and bacterial clearance in Crohn's disease
-
Smith A.M., Rahman F.Z., Hayee B.H., Graham S.J., Marks D.J.B., Sewell G.W., Palmer C.D., Wilde J., Foxwell B.M.J., Gloger I.S., et al. Disordered macrophage cytokine secretion underlies impaired acute inflammation and bacterial clearance in Crohn's disease. J Exp Med 206 (2009) 1883-1897
-
(2009)
J Exp Med
, vol.206
, pp. 1883-1897
-
-
Smith, A.M.1
Rahman, F.Z.2
Hayee, B.H.3
Graham, S.J.4
Marks, D.J.B.5
Sewell, G.W.6
Palmer, C.D.7
Wilde, J.8
Foxwell, B.M.J.9
Gloger, I.S.10
-
41
-
-
69549121823
-
Revisiting Crohn's disease as a primary immunodeficiency of macrophages
-
Casanova J.L., and Abel L. Revisiting Crohn's disease as a primary immunodeficiency of macrophages. J Exp Med 206 (2009) 1839-1843
-
(2009)
J Exp Med
, vol.206
, pp. 1839-1843
-
-
Casanova, J.L.1
Abel, L.2
-
42
-
-
65249115914
-
A Crohn's disease-associated NOD2 mutation suppresses transcription of human IL10 by inhibiting activity of the nuclear ribonucleoprotein hnRNP-A1
-
Noguchi E., Homma Y., Kang X., Netea M.G., and Ma X. A Crohn's disease-associated NOD2 mutation suppresses transcription of human IL10 by inhibiting activity of the nuclear ribonucleoprotein hnRNP-A1. Nat Immunol 10 (2009) 471-479
-
(2009)
Nat Immunol
, vol.10
, pp. 471-479
-
-
Noguchi, E.1
Homma, Y.2
Kang, X.3
Netea, M.G.4
Ma, X.5
-
43
-
-
35548956882
-
Immunology in natura: clinical, epidemiological and evolutionary genetics of infectious diseases
-
Quintana-Murci L., Alcais A., Abel L., and Casanova J.L. Immunology in natura: clinical, epidemiological and evolutionary genetics of infectious diseases. Nat Immunol 8 (2007) 1165-1171
-
(2007)
Nat Immunol
, vol.8
, pp. 1165-1171
-
-
Quintana-Murci, L.1
Alcais, A.2
Abel, L.3
Casanova, J.L.4
-
44
-
-
57449096122
-
A prescription for human immunology
-
Davis M.M. A prescription for human immunology. Immunity 29 (2008) 835-838
-
(2008)
Immunity
, vol.29
, pp. 835-838
-
-
Davis, M.M.1
-
45
-
-
44049084451
-
The habitual, diverse and surmountable obstacles to human immunology research
-
Hayday A.C., and Peakman M. The habitual, diverse and surmountable obstacles to human immunology research. Nat Immunol 9 (2008) 575-580
-
(2008)
Nat Immunol
, vol.9
, pp. 575-580
-
-
Hayday, A.C.1
Peakman, M.2
-
46
-
-
70349734609
-
Pulmonary alveolar proteinosis, a primary immunodeficiency of impaired GM-CSF stimulation of macrophages
-
Trapnell B.C., Carey B.C., Uchida K., and Suzuki T. Pulmonary alveolar proteinosis, a primary immunodeficiency of impaired GM-CSF stimulation of macrophages. Curr Opin Immunol 21 (2009) 514-521
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 514-521
-
-
Trapnell, B.C.1
Carey, B.C.2
Uchida, K.3
Suzuki, T.4
-
47
-
-
58149316253
-
Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1
-
Martinez-Moczygemba M., Doan M.L., Elidemir O., Fan L.L., Cheung S.W., Lei J.T., Moore J.P., Tavana G., Lewis L.R., Zhu Y., et al. Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1. J Exp Med 205 (2008) 2711-2716
-
(2008)
J Exp Med
, vol.205
, pp. 2711-2716
-
-
Martinez-Moczygemba, M.1
Doan, M.L.2
Elidemir, O.3
Fan, L.L.4
Cheung, S.W.5
Lei, J.T.6
Moore, J.P.7
Tavana, G.8
Lewis, L.R.9
Zhu, Y.10
-
48
-
-
58149313016
-
Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA
-
Suzuki T., Sakagami T., Rubin B.K., Nogee L.M., Wood R.E., Zimmerman S.L., Smolarek T., Dishop M.K., Wert S.E., Whitsett J.A., et al. Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA. J Exp Med 205 (2008) 2703-2710
-
(2008)
J Exp Med
, vol.205
, pp. 2703-2710
-
-
Suzuki, T.1
Sakagami, T.2
Rubin, B.K.3
Nogee, L.M.4
Wood, R.E.5
Zimmerman, S.L.6
Smolarek, T.7
Dishop, M.K.8
Wert, S.E.9
Whitsett, J.A.10
-
49
-
-
0033588819
-
Idiopathic pulmonary alveolar proteinosis as an autoimmune disease with neutralizing antibody against granulocyte/macrophage colony-stimulating factor
-
Kitamura T., Tanaka N., Watanabe J., Uchida, Kanegasaki S., Yamada Y., and Nakata K. Idiopathic pulmonary alveolar proteinosis as an autoimmune disease with neutralizing antibody against granulocyte/macrophage colony-stimulating factor. J Exp Med 190 (1999) 875-880
-
(1999)
J Exp Med
, vol.190
, pp. 875-880
-
-
Kitamura, T.1
Tanaka, N.2
Watanabe, J.3
Uchida4
Kanegasaki, S.5
Yamada, Y.6
Nakata, K.7
-
50
-
-
58149296183
-
Out of breath: GM-CSFRalpha mutations disrupt surfactant homeostasis
-
Notarangelo L.D., and Pessach I. Out of breath: GM-CSFRalpha mutations disrupt surfactant homeostasis. J Exp Med 205 (2008) 2693-2697
-
(2008)
J Exp Med
, vol.205
, pp. 2693-2697
-
-
Notarangelo, L.D.1
Pessach, I.2
-
51
-
-
40449106777
-
Recurrent staphylococcal cellulitis and subcutaneous abscesses in a child with autoantibodies against IL-6
-
Puel A., Picard C., Lorrot M., Pons C., Chrabieh M., Lorenzo L., Mamani-Matsuda M., Jouanguy E., Gendrel D., and Casanova J.L. Recurrent staphylococcal cellulitis and subcutaneous abscesses in a child with autoantibodies against IL-6. J Immunol 180 (2008) 647-654
-
(2008)
J Immunol
, vol.180
, pp. 647-654
-
-
Puel, A.1
Picard, C.2
Lorrot, M.3
Pons, C.4
Chrabieh, M.5
Lorenzo, L.6
Mamani-Matsuda, M.7
Jouanguy, E.8
Gendrel, D.9
Casanova, J.L.10
-
52
-
-
24644486557
-
Acquired predisposition to mycobacterial disease due to autoantibodies to IFN-gamma
-
Kampmann B., Hemingway C., Stephens A., Davidson R., Goodsall A., Anderson S., Nicol M., Scholvinck E., Relman D., Waddell S., et al. Acquired predisposition to mycobacterial disease due to autoantibodies to IFN-gamma. J Clin Invest 115 (2005) 2480-2488
-
(2005)
J Clin Invest
, vol.115
, pp. 2480-2488
-
-
Kampmann, B.1
Hemingway, C.2
Stephens, A.3
Davidson, R.4
Goodsall, A.5
Anderson, S.6
Nicol, M.7
Scholvinck, E.8
Relman, D.9
Waddell, S.10
-
53
-
-
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., Feinberg J., Jouanguy E., Boisson-Dupuis S., Fieschi C., Picard C., et al. Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features. Semin Immunol 18 (2006) 347-361
-
(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
Feinberg, J.6
Jouanguy, E.7
Boisson-Dupuis, S.8
Fieschi, C.9
Picard, C.10
-
54
-
-
42649085344
-
Forward genetic dissection of immunity to infection in the mouse
-
Vidal S.M., Malo D., Marquis J.F., and Gros P. Forward genetic dissection of immunity to infection in the mouse. Annu Rev Immunol 26 (2008) 81-132
-
(2008)
Annu Rev Immunol
, vol.26
, pp. 81-132
-
-
Vidal, S.M.1
Malo, D.2
Marquis, J.F.3
Gros, P.4
-
55
-
-
22944461763
-
Inborn errors of immunity to infection: the rule rather than the exception
-
Casanova J.L., and Abel L. Inborn errors of immunity to infection: the rule rather than the exception. J Exp Med 202 (2005) 197-201
-
(2005)
J Exp Med
, vol.202
, pp. 197-201
-
-
Casanova, J.L.1
Abel, L.2
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