-
1
-
-
0033522220
-
Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder
-
Grimbacher B, Holland SM, Gallin JI, Greenberg F, Hill SC, Malech HL, et al. Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder. N Engl J Med 1999;340:692-702
-
(1999)
N Engl J Med
, vol.340
, pp. 692-702
-
-
Grimbacher, B.1
Holland, S.M.2
Gallin, J.I.3
Greenberg, F.4
Hill, S.C.5
Malech, H.L.6
-
2
-
-
9144261081
-
Autosomal recessive hyperimmunoglobulin
-
Renner ED, Puck JM, Holland SM, Schmitt M, Weiss M, Frosch M, et al. Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity. J Pediatr 2004;144:93-9
-
(2004)
E Syndrome: A Distinct Disease Entity. J Pediatr
, vol.144
, pp. 93-99
-
-
Renner, E.D.1
Puck, J.M.2
Holland, S.M.3
Schmitt, M.4
Weiss, M.5
Frosch, M.6
-
3
-
-
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, et al. Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity. Immunity 2006;25:745-55
-
(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
-
4
-
-
35348960378
-
STAT3 mutations in the hyper-IgE syndrome
-
Holland SM, DeLeo FR, Elloumi HZ, Hsu AP, Uzel G, Brodsky N, et al. STAT3 mutations in the hyper-IgE syndrome. N Engl J Med 2007;357:1608-19
-
(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
-
5
-
-
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, et al. Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature 2007;448:1058-62
-
(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
-
7
-
-
34547108380
-
JAK-STAT signaling: From interferons to cytokines
-
Schindler C, Levy DE, Decker T. JAK-STAT signaling: from interferons to cytokines. J Biol Chem 2007;282:20059-63
-
(2007)
J Biol Chem
, vol.282
, pp. 20059-20063
-
-
Schindler, C.1
Levy, D.E.2
Decker, T.3
-
8
-
-
76049116822
-
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome
-
Woellner C, Gertz EM, Schäffer AA, Lagos M, Perro M, Glocker EO, et al. Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome. J Allergy Clin Immunol 2010;125:424-32
-
(2010)
J Allergy Clin Immunol
, vol.125
, pp. 424-432
-
-
Woellner, C.1
Gertz, E.M.2
Schäffer, A.A.3
Lagos, M.4
Perro, M.5
Glocker, E.O.6
-
9
-
-
67651225115
-
Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome
-
Al Khatib S, Keles S, Garcia-Lloret M, Karakoc-Aydiner E, Reisli I, Artac H, et al. Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome. J Allergy Clin Immunol 2009;124:342-8
-
(2009)
J Allergy Clin Immunol
, vol.124
, pp. 342-348
-
-
Al Khatib, S.1
Keles, S.2
Garcia-Lloret, M.3
Karakoc-Aydiner, E.4
Reisli, I.5
Artac, H.6
-
11
-
-
84859972127
-
JAK and STAT signaling molecules in immunoregulation and immune-mediated disease
-
O'Shea JJ, Plenge R. JAK and STAT signaling molecules in immunoregulation and immune-mediated disease. Immunity 2012;36:542-50
-
(2012)
Immunity
, vol.36
, pp. 542-550
-
-
O'shea, J.J.1
Plenge, R.2
-
12
-
-
41449110468
-
Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
-
Milner JD, Brenchley JM, Laurence A, Freeman AF, Hill BJ, Elias KM, et al. Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome. Nature 2008;452:773-6
-
(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
-
13
-
-
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, et al. Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells. J Exp Med 2008;205:1543-50
-
(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
-
14
-
-
46949089128
-
Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3
-
Ma CS, Chew GY, Simpson N, Priyadarshi A, Wong M, Grimbacher B, et al. Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3. J Exp Med 2008;205:1551-7
-
(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
-
15
-
-
46049106939
-
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome
-
Renner ED, Rylaarsdam S, Anover-Sombke S, Rack AL, Reichenbach J, Carey JC, et al. Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome. J Allergy Clin Immunol 2008;122:181-7
-
(2008)
J Allergy Clin Immunol
, vol.122
, pp. 181-187
-
-
Renner, E.D.1
Rylaarsdam, S.2
Anover-Sombke, S.3
Rack, A.L.4
Reichenbach, J.5
Carey, J.C.6
-
16
-
-
74549186432
-
Th1-Th17 cells mediate protective adaptive immunity against Staphylococcus aureus and Candida albicans infection in mice
-
Lin L, Ibrahim AS, Xu X, Farber JM, Avanesian V, Baquir B, et al. Th1-Th17 cells mediate protective adaptive immunity against Staphylococcus aureus and Candida albicans infection in mice. PLoS Pathog 2009;5:1000703
-
(2009)
Plos Pathog
, vol.5
-
-
Lin, L.1
Ibrahim, A.S.2
Xu, X.3
Farber, J.M.4
Avanesian, V.5
Baquir, B.6
-
17
-
-
79953284685
-
Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity
-
Puel A, Cypowyj S, Bustamante J, Wright JF, Liu L, Lim HK, et al. Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity. Science 2011;332:65-8
-
(2011)
Science
, vol.332
, pp. 65-68
-
-
Puel, A.1
Cypowyj, S.2
Bustamante, J.3
Wright, J.F.4
Liu, L.5
Lim, H.K.6
-
18
-
-
71149115670
-
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
-
Engelhardt KR, McGhee S, Winkler S, Sassi A, Woellner C, Lopez-Herrera G, et al. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome. J Allergy Clin Immunol 2009;124:1289-302
-
(2009)
J Allergy Clin Immunol
, vol.124
, pp. 1289-1302
-
-
Engelhardt, K.R.1
McGhee, S.2
Winkler, S.3
Sassi, A.4
Woellner, C.5
Lopez-Herrera, G.6
-
19
-
-
70949098060
-
Combined immunodeficiency associated with DOCK8 mutations
-
Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med 2009;361:2046-55
-
(2009)
N Engl J Med
, vol.361
, pp. 2046-2055
-
-
Zhang, Q.1
Davis, J.C.2
Lamborn, I.T.3
Freeman, A.F.4
Jing, H.5
Favreau, A.J.6
-
20
-
-
70449718702
-
Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production
-
Randall KL, Lambe T, Johnson AL, Treanor B, Kucharska E, Domaschenz H, et al. Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production. Nat Immunol 2009;10:1283-91
-
(2009)
Nat Immunol
, vol.10
, pp. 1283-1291
-
-
Randall, K.L.1
Lambe, T.2
Johnson, A.L.3
Treanor, B.4
Kucharska, E.5
Domaschenz, H.6
-
21
-
-
84938738886
-
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
-
Engelhardt KR, Gertz ME, Keles S, Schäffer AA, Sigmund EC, Glocker C, et al. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol 2015;136:402-12
-
(2015)
J Allergy Clin Immunol
, vol.136
, pp. 402-412
-
-
Engelhardt, K.R.1
Gertz, M.E.2
Keles, S.3
Schäffer, A.A.4
Sigmund, E.C.5
Glocker, C.6
-
22
-
-
84863985331
-
Additional diverse findings expand the clinical presentation of DOCK8 deficiency
-
Sanal O, Jing H, Ozgur T, Ayvaz D, Strauss-Albee DM, Ersoy-Evans S, et al. Additional diverse findings expand the clinical presentation of DOCK8 deficiency. J Clin Immunol 2012;32:698-708
-
(2012)
J Clin Immunol
, vol.32
, pp. 698-708
-
-
Sanal, O.1
Jing, H.2
Ozgur, T.3
Ayvaz, D.4
Strauss-Albee, D.M.5
Ersoy-Evans, S.6
-
23
-
-
84901777686
-
Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype
-
Jing H, Zhang Q, Zhang Y, Hill BJ, Dove CG, Gelfand EW, et al. Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype. J Allergy Clin Immunol 2014;133:1667-75
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1667-1675
-
-
Jing, H.1
Zhang, Q.2
Zhang, Y.3
Hill, B.J.4
Dove, C.G.5
Gelfand, E.W.6
-
24
-
-
84925543370
-
DOCK8 deficiency: Clinical and immunological phenotype and treatment options -a review of 136 patients
-
Aydin SE, Kilic SS, Aytekin C, Kumar A, Porras O, Kainulainen L, et al. DOCK8 deficiency: clinical and immunological phenotype and treatment options -a review of 136 patients. J Clin Immunol 2015;35:189-98
-
(2015)
J Clin Immunol
, vol.35
, pp. 189-198
-
-
Aydin, S.E.1
Kilic, S.S.2
Aytekin, C.3
Kumar, A.4
Porras, O.5
Kainulainen, L.6
-
25
-
-
84876441426
-
Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: Single center experience of twenty-five patients
-
Alsum Z, Hawwari A, Alsmadi O, Al-Hissi S, Borrero E, Abu-Staiteh A, et al. Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients. J Clin Immunol 2013;33:55-67
-
(2013)
J Clin Immunol
, vol.33
, pp. 55-67
-
-
Alsum, Z.1
Hawwari, A.2
Alsmadi, O.3
Al-Hissi, S.4
Borrero, E.5
Abu-Staiteh, A.6
-
27
-
-
34548472221
-
GEF what? Dock180 and related proteins help Rac to polarize cells in new ways
-
Côté JF, Vuori K. GEF what? Dock180 and related proteins help Rac to polarize cells in new ways. Trends Cell Biol 2007;17:383-93
-
(2007)
Trends Cell Biol
, vol.17
, pp. 383-393
-
-
Côté, J.F.1
Vuori, K.2
-
28
-
-
84931403287
-
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections
-
Dobbs K, Domínguez Conde C, Zhang SY, Parolini S, Audry M, Chou J, et al. Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections. N Engl J Med 2015;372:2409-22
-
(2015)
N Engl J Med
, vol.372
, pp. 2409-2422
-
-
Dobbs, K.1
Domínguez Conde, C.2
Zhang, S.Y.3
Parolini, S.4
Audry, M.5
Chou, J.6
-
29
-
-
79960140401
-
Multiple factors confer specific Cdc42 and Rac protein activation by dedicator of cytokinesis (DOCK) nucleotide exchange factors
-
Kulkarni K, Yang J, Zhang Z, Barford D. Multiple factors confer specific Cdc42 and Rac protein activation by dedicator of cytokinesis (DOCK) nucleotide exchange factors. J Biol Chem 2011;286:25341-51
-
(2011)
J Biol Chem
, vol.286
, pp. 25341-25351
-
-
Kulkarni, K.1
Yang, J.2
Zhang, Z.3
Barford, D.4
-
30
-
-
70249105718
-
Activation of Rho GTPases by DOCK exchange factors is mediated by a nucleotide sensor
-
Yang J, Zhang Z, Roe SM, Marshall CJ, Barford D. Activation of Rho GTPases by DOCK exchange factors is mediated by a nucleotide sensor. Science 2009;325:1398-402
-
(2009)
Science
, vol.325
, pp. 1398-1402
-
-
Yang, J.1
Zhang, Z.2
Roe, S.M.3
Marshall, C.J.4
Barford, D.5
-
31
-
-
78650662845
-
DOCK8 immune deficiency as a model for primary cytoskeletal dysfunction
-
McGhee SA, Chatila TA. DOCK8 immune deficiency as a model for primary cytoskeletal dysfunction. Dis Markers 2010;29:151-6
-
(2010)
Dis Markers
, vol.29
, pp. 151-156
-
-
McGhee, S.A.1
Chatila, T.A.2
-
32
-
-
84861078339
-
DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses
-
Harada Y, Tanaka Y, Terasawa M, Pieczyk M, Habiro K, Katakai T, et al. DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses. Blood 2012;119:4451-61
-
(2012)
Blood
, vol.119
, pp. 4451-4461
-
-
Harada, Y.1
Tanaka, Y.2
Terasawa, M.3
Pieczyk, M.4
Habiro, K.5
Katakai, T.6
-
33
-
-
84875226021
-
Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency
-
Mizesko MC, Banerjee PP, Monaco-Shawver L, Mace EM, Bernal WE, Sawalle-Belohradsky J, et al. Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol 2013;131:840-8
-
(2013)
J Allergy Clin Immunol
, vol.131
, pp. 840-848
-
-
Mizesko, M.C.1
Banerjee, P.P.2
Monaco-Shawver, L.3
Mace, E.M.4
Bernal, W.E.5
Sawalle-Belohradsky, J.6
-
34
-
-
84875454223
-
Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity
-
Ham H, Guerrier S, Kim J, Schoon RA, Anderson EL, Hamann MJ, et al. Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity. J Immunol 2013;190:3661-9
-
(2013)
J Immunol
, vol.190
, pp. 3661-3669
-
-
Ham, H.1
Guerrier, S.2
Kim, J.3
Schoon, R.A.4
Erson, E.L.5
Hamann, M.J.6
-
35
-
-
80055107954
-
DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice
-
Randall KL, Chan SS, Ma CS, Fung I, Mei Y, Yabas M, et al. DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice. J Exp Med 2011;208:2305-20
-
(2011)
J Exp Med
, vol.208
, pp. 2305-2320
-
-
Randall, K.L.1
Chan, S.S.2
Ma, C.S.3
Fung, I.4
Mei, Y.5
Yabas, M.6
-
36
-
-
84924283592
-
DOCK8 regulates lymphocyte shape integrity for skin antiviral immunity
-
Zhang Q, Dove CG, Hor JL, Murdock HM, Strauss-Albee DM, Garcia JA, et al. DOCK8 regulates lymphocyte shape integrity for skin antiviral immunity. J Exp Med 2014;211:2549-66
-
(2014)
J Exp Med
, vol.211
, pp. 2549-2566
-
-
Zhang, Q.1
Dove, C.G.2
Hor, J.L.3
Murdock, H.M.4
Strauss-Albee, D.M.5
Garcia, J.A.6
-
37
-
-
84861236002
-
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation
-
Jabara HH, McDonald DR, Janssen E, Massaad MJ, Ramesh N, Borzutzky A, et al. DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation. Nat Immunol 2012;13:612-20
-
(2012)
Nat Immunol
, vol.13
, pp. 612-620
-
-
Jabara, H.H.1
McDonald, D.R.2
Janssen, E.3
Massaad, M.J.4
Ramesh, N.5
Borzutzky, A.6
-
38
-
-
80054842183
-
Deficient T Cell Receptor Excision Circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: Implications for pathogenesis and potential detection by newborn screening
-
Dasouki M, Okonkwo KC, Ray A, Folmsbeel CK, Gozales D, Keles S, et al. Deficient T Cell Receptor Excision Circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: implications for pathogenesis and potential detection by newborn screening. Clin Immunol 2011;141:128-32
-
(2011)
Clin Immunol
, vol.141
, pp. 128-132
-
-
Dasouki, M.1
Okonkwo, K.C.2
Ray, A.3
Folmsbeel, C.K.4
Gozales, D.5
Keles, S.6
-
39
-
-
84907336842
-
DOCK8 regulates protective immunity by controlling the function and survival of RORγt+ ILCs
-
Singh AK, Eken A, Fry M, Bettelli E, Oukka M. DOCK8 regulates protective immunity by controlling the function and survival of RORγt+ ILCs. Nat Commun 2014;5:4603
-
(2014)
Nat Commun
, vol.5
, pp. 4603
-
-
Singh, A.K.1
Eken, A.2
Fry, M.3
Bettelli, E.4
Oukka, M.5
-
40
-
-
84940547063
-
The microbiota regulates type 2 immunity through RORγt+ T cells
-
Ohnmacht C, Park JH, Cording S, Wing JB, Atarashi K, Obata Y, et al. The microbiota regulates type 2 immunity through RORγt+ T cells. Science 2015
-
(2015)
Science
-
-
Ohnmacht, C.1
Park, J.H.2
Cording, S.3
Wing, J.B.4
Atarashi, K.5
Obata, Y.6
-
41
-
-
84908440532
-
Dedicator of cytokinesis 8-deficient patients have a breakdown in peripheral B-cell tolerance and defective regulatory T cells
-
Janssen E, Morbach H, Ullas S, Bannock JM, Massad C, Menard L, et al. Dedicator of cytokinesis 8-deficient patients have a breakdown in peripheral B-cell tolerance and defective regulatory T cells. J Allergy Clin Immunol 2014;134:1365-74
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1365-1374
-
-
Janssen, E.1
Morbach, H.2
Ullas, S.3
Bannock, J.M.4
Massad, C.5
Menard, L.6
-
42
-
-
84925038493
-
Regulatory T cell reprogramming toward a Th2-cell-like lineage impairs oral tolerance and promotes food allergy
-
Noval Rivas M, Burton OT, Wise P, Charbonnier LM, Georgiev P, Oettgen HC, et al. Regulatory T cell reprogramming toward a Th2-cell-like lineage impairs oral tolerance and promotes food allergy. Immunity 2015;42:512-23
-
(2015)
Immunity
, vol.42
, pp. 512-523
-
-
Noval Rivas, M.1
Burton, O.T.2
Wise, P.3
Charbonnier, L.M.4
Georgiev, P.5
Oettgen, H.C.6
-
43
-
-
84901807538
-
Plasmacytoid dendritic cell depletion in DOCK8 deficiency: Rescue of severe herpetic infections with IFN-α 2b therapy
-
Keles S, Jabara HH, Reisli I, McDonald DR, Barlan I, Hanna-Wakim R, et al. Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-α 2b therapy. J Allergy Clin Immunol 2014;133:1753-5
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1753-1755
-
-
Keles, S.1
Jabara, H.H.2
Reisli, I.3
McDonald, D.R.4
Barlan, I.5
Hanna-Wakim, R.6
-
44
-
-
85027940079
-
Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation
-
Siegel AM, Stone KD, Cruse G, Lawrence MG, Olivera A, Jung MY, et al. Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation. J Allergy Clin Immunol 2013;132:1388-96
-
(2013)
J Allergy Clin Immunol
, vol.132
, pp. 1388-1396
-
-
Siegel, A.M.1
Stone, K.D.2
Cruse, G.3
Lawrence, M.G.4
Olivera, A.5
Jung, M.Y.6
-
45
-
-
84892474895
-
Flow cytometry biomarkers distinguish DOCK8 deficiency from severe atopic dermatitis
-
Janssen E, Tsitsikov E, Al-Herz W, Lefranc G, Megarbane A, Dasouki M, et al. Flow cytometry biomarkers distinguish DOCK8 deficiency from severe atopic dermatitis. Clin Immunol 2014;150:220-4
-
(2014)
Clin Immunol
, vol.150
, pp. 220-224
-
-
Janssen, E.1
Tsitsikov, E.2
Al-Herz, W.3
Lefranc, G.4
Megarbane, A.5
Dasouki, M.6
-
46
-
-
84903751001
-
Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency
-
Pai SY, de Boer H, Massaad MJ, Chatila TA, Keles S, Jabara HH, et al. Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency. J Allergy Clin Immunol 2014;134:221-3
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 221-223
-
-
Pai, S.Y.1
De Boer, H.2
Massaad, M.J.3
Chatila, T.A.4
Keles, S.5
Jabara, H.H.6
-
47
-
-
84899692269
-
Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency
-
Al-Zahrani D, Raddadi A, Massaad M, Keles S, Jabara HH, Chatila TA, et al. Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency. Clin Immunol 2014;153:104-8
-
(2014)
Clin Immunol
, vol.153
, pp. 104-108
-
-
Al-Zahrani, D.1
Raddadi, A.2
Massaad, M.3
Keles, S.4
Jabara, H.H.5
Chatila, T.A.6
-
48
-
-
84899645392
-
Beneficial IFN-α treatment of tumorous herpes simplex blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency
-
Papan C, Hagl B, Heinz V, Albert MH, Ehrt O, Sawalle-Belohradsky J, et al. Beneficial IFN-α treatment of tumorous herpes simplex blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol 2014;133:1456-8
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1456-1458
-
-
Papan, C.1
Hagl, B.2
Heinz, V.3
Albert, M.H.4
Ehrt, O.5
Sawalle-Belohradsky, J.6
-
49
-
-
84861194430
-
Successful bone marrow transplantation for DOCK8 deficient hyper IgE syndrome
-
Metin A, Tavil B, Azık F, Azkur D, Ok-Bozkaya I, Kocabas C, et al. Successful bone marrow transplantation for DOCK8 deficient hyper IgE syndrome. Pediatr Transplant 2012;16:398-9
-
(2012)
Pediatr Transplant
, vol.16
, pp. 398-399
-
-
Metin, A.1
Tavil, B.2
Azık, F.3
Azkur, D.4
Ok-Bozkaya, I.5
Kocabas, C.6
-
50
-
-
78649878923
-
Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomalrecessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency
-
McDonald DR, Massaad MJ, Johnston A, Keles S, Chatila T, Geha RS, et al. Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomalrecessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol 2010;126:1304-5
-
(2010)
J Allergy Clin Immunol
, vol.126
, pp. 1304-1305
-
-
McDonald, D.R.1
Massaad, M.J.2
Johnston, A.3
Keles, S.4
Chatila, T.5
Geha, R.S.6
-
51
-
-
79953734130
-
Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation
-
Gatz SA, Benninghoff U, Schütz C, Schulz A, Hönig M, Pannicke U, et al. Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation. Bone Marrow Transplant 2011;46:552-6
-
(2011)
Bone Marrow Transplant
, vol.46
, pp. 552-556
-
-
Gatz, S.A.1
Benninghoff, U.2
Schütz, C.3
Schulz, A.4
Hönig, M.5
Pannicke, U.6
-
52
-
-
84928389399
-
Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome
-
Hacein-Bey Abina S, Gaspar HB, Blondeau J, Caccavelli L, Charrier S, Buckland K, et al. Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome. JAMA 2015;313:1550-63.
-
(2015)
JAMA
, vol.313
, pp. 1550-1563
-
-
Hacein-Bey Abina, S.1
Gaspar, H.B.2
Blondeau, J.3
Caccavelli, L.4
Charrier, S.5
Buckland, K.6
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