-
1
-
-
80955148980
-
Hyperimmunoglobulin e syndromes in pediatrics
-
Zhang Q, Su HC. Hyperimmunoglobulin E syndromes in pediatrics. Curr Opin Pediatr. 2011;23(6):653-658.
-
(2011)
Curr Opin Pediatr
, vol.23
, Issue.6
, pp. 653-658
-
-
Zhang, Q.1
Su, H.C.2
-
2
-
-
35348960378
-
STAT3mutations in the hyper-IgE syndrome
-
Holland SM,DeLeo FR, ElloumiHZ, et al. STAT3mutations in the hyper-IgE syndrome.NEnglJMed. 2007;357(16):1608-1619.
-
(2007)
N Engl J Med
, vol.357
, Issue.16
, pp. 1608-1619
-
-
Holland, S.M.1
Deleo, F.R.2
Elloumi, H.Z.3
-
3
-
-
34548317417
-
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
-
Minegishi Y, Saito M, Tsuchiya S, et al. Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature. 2007;448(7157):1058-1062.
-
(2007)
Nature
, vol.448
, Issue.7157
, pp. 1058-1062
-
-
Minegishi, Y.1
Saito, M.2
Tsuchiya, S.3
-
4
-
-
70949098060
-
Combined immunodeficiency associated with DOCK8 mutations
-
Zhang Q, Davis JC, Lamborn IT, et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med. 2009;361(21):2046-2055.
-
(2009)
N Engl J Med
, vol.361
, Issue.21
, pp. 2046-2055
-
-
Zhang, Q.1
Davis, J.C.2
Lamborn, I.T.3
-
5
-
-
9144261081
-
Autosomal recessive hyperimmunoglobulin e syndrome: A distinct disease entity
-
Renner ED, Puck JM, Holland SM, et al. Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity. J Pediatr. 2004;144(1):93-99.
-
(2004)
J Pediatr
, vol.144
, Issue.1
, pp. 93-99
-
-
Renner, E.D.1
Puck, J.M.2
Holland, S.M.3
-
6
-
-
71149115670
-
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive formof hyper-IgE syndrome
-
e1284
-
Engelhardt KR,McGhee S, Winkler S, et al. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive formof hyper-IgE syndrome. JAllergyClin Immunol. 2009;124(6):1289-1302, e1284.
-
(2009)
JAllergyClin Immunol
, vol.124
, Issue.6
, pp. 1289-1302
-
-
Engelhardt, K.R.1
McGhee, S.2
Winkler, S.3
-
7
-
-
33845897463
-
Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity
-
Minegishi Y, SaitoM,Morio T, et al. Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity. Immunity. 2006;25(5):745-755.
-
(2006)
Immunity
, vol.25
, Issue.5
, pp. 745-755
-
-
Minegishi, Y.1
Saito, M.2
Morio, T.3
-
8
-
-
78650662845
-
DOCK8 immune deficiency as amodel for primary cytoskeletal dysfunction
-
McGhee SA, Chatila TA.DOCK8 immune deficiency as amodel for primary cytoskeletal dysfunction. Dis Markers. 2010;29(3-4):151-156.
-
(2010)
Dis Markers
, vol.29
, Issue.3-4
, pp. 151-156
-
-
McGhee, S.A.1
Chatila, T.A.2
-
10
-
-
78650649691
-
The essential role of DOCK8 in humoral immunity
-
Randall KL, Lambe T, Goodnow CC, et al. The essential role of DOCK8 in humoral immunity. Dis Markers. 2010;29(3-4):141-150.
-
(2010)
Dis Markers
, vol.29
, Issue.3-4
, pp. 141-150
-
-
Randall, K.L.1
Lambe, T.2
Goodnow, C.C.3
-
11
-
-
79961014871
-
Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency
-
e422
-
Barlogis V, Galambrun C, Chambost H, et al. Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency. J Allergy Clin Immunol. 2011;128(2):420-422, e422.
-
(2011)
J Allergy Clin Immunol
, vol.128
, Issue.2
, pp. 420-422
-
-
Barlogis, V.1
Galambrun, C.2
Chambost, H.3
-
12
-
-
78349303895
-
Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation
-
Bittner TC, Pannicke U, Renner ED, et al. Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation. Klin Padiatr. 2010;222(6):351-355.
-
(2010)
Klin Padiatr
, vol.222
, Issue.6
, pp. 351-355
-
-
Bittner, T.C.1
Pannicke, U.2
Renner, E.D.3
-
13
-
-
79953734130
-
Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation
-
Gatz SA, Benninghoff U, Schutz C, et al. Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation. Bone Marrow Transplant. 2011;46(4):552-556.
-
(2011)
Bone Marrow Transplant
, vol.46
, Issue.4
, pp. 552-556
-
-
Gatz, S.A.1
Benninghoff, U.2
Schutz, C.3
-
14
-
-
78649878923
-
Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency
-
e1303
-
McDonald DR, Massaad MJ, Johnston A, et al. Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol. 2010;126(6):1304-1305, e1303.
-
(2010)
J Allergy Clin Immunol
, vol.126
, Issue.6
, pp. 1304-1305
-
-
McDonald, D.R.1
Massaad, M.J.2
Johnston, A.3
-
15
-
-
84861194430
-
Successful bonemarrowtransplantation forDOCK8 deficient hyper IgE syndrome
-
Metin A, Tavil B, Azik F, et al. Successful bonemarrowtransplantation forDOCK8 deficient hyper IgE syndrome. Pediatr Transplant. 2012;16(4):398-399.
-
(2012)
Pediatr Transplant
, vol.16
, Issue.4
, pp. 398-399
-
-
Metin, A.1
Tavil, B.2
Azik, F.3
-
16
-
-
84857997026
-
Early recipient chimerism testing in the T-and NK-cell lineages for risk assessment of graft rejection in pediatric patients undergoing allogeneic stem cell transplantation
-
Breuer S, Preuner S, Fritsch G, et al. Early recipient chimerism testing in the T-and NK-cell lineages for risk assessment of graft rejection in pediatric patients undergoing allogeneic stem cell transplantation. Leukemia. 2012;26(3):509-519.
-
(2012)
Leukemia
, vol.26
, Issue.3
, pp. 509-519
-
-
Breuer, S.1
Preuner, S.2
Fritsch, G.3
-
17
-
-
84863985331
-
Additional diverse findings expand the clinical presentation ofDOCK8 deficiency
-
SanalO, JingH,Ozgur T, et al. Additional diverse findings expand the clinical presentation ofDOCK8 deficiency. J Clin Immunol. 2012;32(4):698-708.
-
(2012)
J Clin Immunol
, vol.32
, Issue.4
, pp. 698-708
-
-
Sanal, O.1
Jing, H.2
Ozgur, T.3
-
18
-
-
84861235270
-
Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait
-
Al-Herz W, Ragupathy R, Massaad MJ, et al. Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait. Clin Immunol. 2012;143(3):266-272.
-
(2012)
Clin Immunol
, vol.143
, Issue.3
, pp. 266-272
-
-
Al-Herz, W.1
Ragupathy, R.2
Massaad, M.J.3
-
19
-
-
84859796684
-
Molecular diagnosis andmanagement of viral infections in hematopoietic stem cell transplant recipients
-
Breuer S, RauchM,Matthes-Martin S, et al.Molecular diagnosis andmanagement of viral infections in hematopoietic stem cell transplant recipients. Mol Diagn Ther. 2012;16(2):63-77.
-
(2012)
Mol Diagn Ther
, vol.16
, Issue.2
, pp. 63-77
-
-
Breuer, S.1
Rauch, M.2
Matthes-Martin, S.3
-
20
-
-
78650311465
-
Diagnosis of invasive fungal infections by a real-time panfungal PCR assay in immunocompromised pediatric patients
-
Landlinger C, Preuner S, Baskova L, et al. Diagnosis of invasive fungal infections by a real-time panfungal PCR assay in immunocompromised pediatric patients. Leukemia. 2010;24(12):2032-2038.
-
(2010)
Leukemia
, vol.24
, Issue.12
, pp. 2032-2038
-
-
Landlinger, C.1
Preuner, S.2
Baskova, L.3
-
21
-
-
27744589339
-
Cause of death after allogeneic haematopoietic stem cell transplantation (HSCT) in early leukaemias: An EBMTanalysis of lethal infectious complications and changes over calendar time
-
Gratwohl A, Brand R, Frassoni F, et al. Cause of death after allogeneic haematopoietic stem cell transplantation (HSCT) in early leukaemias: an EBMTanalysis of lethal infectious complications and changes over calendar time. Bone Marrow Transplant. 2005;36(9):757-769.
-
(2005)
Bone Marrow Transplant
, vol.36
, Issue.9
, pp. 757-769
-
-
Gratwohl, A.1
Brand, R.2
Frassoni, F.3
-
22
-
-
0043245804
-
Molecular monitoring of adenovirus in peripheral blood after allogeneic bonemarrowtransplantation permits early diagnosis of disseminated disease
-
Lion T, Baumgartinger R, Watzinger F, et al. Molecular monitoring of adenovirus in peripheral blood after allogeneic bonemarrowtransplantation permits early diagnosis of disseminated disease. Blood. 2003;102(3):1114-1120.
-
(2003)
Blood
, vol.102
, Issue.3
, pp. 1114-1120
-
-
Lion, T.1
Baumgartinger, R.2
Watzinger, F.3
-
23
-
-
59149089046
-
The clinical feature of invasive fungal infection in pediatric patients with hematologic andmalignant diseases: A 10-year analysis at a single institution at Japan
-
Kobayashi R, Kaneda M, Sato T, et al. The clinical feature of invasive fungal infection in pediatric patients with hematologic andmalignant diseases: a 10-year analysis at a single institution at Japan. J Pediatr Hematol Oncol. 2008;30(12):886-890.
-
(2008)
J Pediatr Hematol Oncol
, vol.30
, Issue.12
, pp. 886-890
-
-
Kobayashi, R.1
Kaneda, M.2
Sato, T.3
-
24
-
-
0023231441
-
Acquisition of cytomegalovirus infection from birth to 10 years: A longitudinal serologic study
-
YowMD, White NH, Taber LH, et al. Acquisition of cytomegalovirus infection from birth to 10 years: a longitudinal serologic study. J Pediatr. 1987;110(1):37-42.
-
(1987)
J Pediatr
, vol.110
, Issue.1
, pp. 37-42
-
-
Yow, M.D.1
White, N.H.2
Taber, L.H.3
-
25
-
-
0016768093
-
Epidemiological studies of Epstein-Barr herpesvirus infection inWestern Australia
-
Lai PK, Mackay-Scollay EM, Alpers MP. Epidemiological studies of Epstein-Barr herpesvirus infection inWestern Australia. J Hyg. 1975;74(3):329-337.
-
(1975)
J Hyg
, vol.74
, Issue.3
, pp. 329-337
-
-
Lai, P.K.1
MacKay-Scollay, E.M.2
Alpers, M.P.3
-
26
-
-
77956395504
-
Transplantation of hematopoietic stem cells and longtermsurvival for primary immunodeficiencies in Europe: Entering a new century, do we do better
-
e601-e611
-
Gennery AR, Slatter MA, Grandin L, et al. Transplantation of hematopoietic stem cells and longtermsurvival for primary immunodeficiencies in Europe: entering a new century, do we do better J Allergy Clin Immunol. 2010;126(3):602-610, e601-e611.
-
(2010)
J Allergy Clin Immunol
, vol.126
, Issue.3
, pp. 602-610
-
-
Gennery, A.R.1
Slatter, M.A.2
Grandin, L.3
-
27
-
-
78449249501
-
Dedicator of cytokinesis 8 (DOCK8) deficiency
-
Su HC. Dedicator of cytokinesis 8 (DOCK8) deficiency. Curr Opin Allergy Clin Immunol. 2010;10(6):515-520.
-
(2010)
Curr Opin Allergy Clin Immunol
, vol.10
, Issue.6
, pp. 515-520
-
-
Su, H.C.1
-
28
-
-
84856022081
-
Cutaneous manifestations of DOCK8 deficiency syndrome
-
Chu EY, Freeman AF, Jing H, et al. Cutaneous manifestations of DOCK8 deficiency syndrome. Arch Dermatol. 2012;148(1):79-84.
-
(2012)
Arch Dermatol
, vol.148
, Issue.1
, pp. 79-84
-
-
Chu, E.Y.1
Freeman, A.F.2
Jing, H.3
-
29
-
-
84891488843
-
Management of DOCK8 deficiency by hematopoietic stem cell transplantation
-
Geneva Switzerland; April 3
-
Albert, MH, Aydin SA, Matthes-Martin, S, et al. Management of DOCK8 deficiency by hematopoietic stem cell transplantation. 38th Annual Meeting of the European Group for Blood and Marrow Transplantation. Geneva, Switzerland; April 3, 2012.
-
(2012)
38th Annual Meeting of the European Group for Blood and Marrow Transplantation
-
-
Albert, M.H.1
Aydin, S.A.2
Matthes-Martin, S.3
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