-
1
-
-
84905487884
-
The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiency
-
S.E. Turvey, A. Durandy, A. Fischer, S.Y. Fung, R.S. Geha, A. Gewies, and et al. The CARD11-BCL10-MALT1 (CBM) signalosome complex: stepping into the limelight of human primary immunodeficiency J Allergy Clin Immunol 134 2014 276 284
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 276-284
-
-
Turvey, S.E.1
Durandy, A.2
Fischer, A.3
Fung, S.Y.4
Geha, R.S.5
Gewies, A.6
-
2
-
-
84899620444
-
Combined immunodeficiency associated with homozygous MALT1 mutations
-
1462e1-7
-
M. McKinnon, J. Rozmus, S.Y. Fung, A. Hirschsfield, K.I. Del Bel, L. Thomas, and et al. Combined immunodeficiency associated with homozygous MALT1 mutations J Allergy Clin Immunol 133 2014 1458 1462 1462.e1-7
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1458-1462
-
-
McKinnon, M.1
Rozmus, J.2
Fung, S.Y.3
Hirschsfield, A.4
Del Bel, K.I.5
Thomas, L.6
-
4
-
-
84914166384
-
Intact IL-12 signaling is necessary for the generation of human natural killer cells with enhanced effector function after restimulation
-
V.R. Simhadri, M.L. Mariano, O. Zemarruzabeitia, C.M. Seroogy, S.M. Holland, H.S. Kuehn, and et al. Intact IL-12 signaling is necessary for the generation of human natural killer cells with enhanced effector function after restimulation J Allergy Clin Immunol 134 2014 1190 1193.e1
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1190-1193e1
-
-
Simhadri, V.R.1
Mariano, M.L.2
Zemarruzabeitia, O.3
Seroogy, C.M.4
Holland, S.M.5
Kuehn, H.S.6
-
5
-
-
84903733656
-
MicroRNA-150 regulates the cytotoxicity of natural killers by targeting perforin-1
-
N. Kim, M. Kim, S. Yun, J. Doh, P.D. Greenberg, T.D. Kim, and et al. MicroRNA-150 regulates the cytotoxicity of natural killers by targeting perforin-1 J Allergy Clin Immunol 134 2014 195 203
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 195-203
-
-
Kim, N.1
Kim, M.2
Yun, S.3
Doh, J.4
Greenberg, P.D.5
Kim, T.D.6
-
6
-
-
84905562170
-
Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia and multiple sclerosis
-
H. Sic, H. Kraus, J. Madl, K.A. Flittner, A.L. von Muschow, K. Pieper, and et al. Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia and multiple sclerosis J Allergy Clin Immunol 134 2014 420 428
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 420-428
-
-
Sic, H.1
Kraus, H.2
Madl, J.3
Flittner, K.A.4
Von Muschow, A.L.5
Pieper, K.6
-
7
-
-
84891738469
-
High-content cytometry and transcriptomic biomarker profiling of human B-cell activation
-
C. Hennig, C. Ilginus, K. Boztug, J. Skokowa, L. Marodi, A. Szaflarska, and et al. High-content cytometry and transcriptomic biomarker profiling of human B-cell activation J Allergy Clin Immunol 133 2014 172 180
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 172-180
-
-
Hennig, C.1
Ilginus, C.2
Boztug, K.3
Skokowa, J.4
Marodi, L.5
Szaflarska, A.6
-
8
-
-
84905584621
-
Analysis of somatic hypermutation in the IgM switch region in human B cells
-
K. Horiuchi, K. Imai, K. Mitsui-Sekinaka, T.W. Yeh, H. Ochs, A. Durandy, and et al. Analysis of somatic hypermutation in the IgM switch region in human B cells J Allergy Clin Immunol 134 2014 411 419
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 411-419
-
-
Horiuchi, K.1
Imai, K.2
Mitsui-Sekinaka, K.3
Yeh, T.W.4
Ochs, H.5
Durandy, A.6
-
9
-
-
84903730984
-
Human CD19 and CD40L deficiencies impair antibody selection and differentially affect somatic hypermutation
-
M.C. Van Zelm, S.J. Bartol, G.J. Driessen, F. Mascart, I. Reisli, J.L. Franco, and et al. Human CD19 and CD40L deficiencies impair antibody selection and differentially affect somatic hypermutation J Allergy Clin Immunol 134 2014 135 144
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 135-144
-
-
Van Zelm, M.C.1
Bartol, S.J.2
Driessen, G.J.3
Mascart, F.4
Reisli, I.5
Franco, J.L.6
-
10
-
-
84897421218
-
Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire development
-
X. Yu, J.R. Almeida, S. Darko, M. van der Burg, S.S. Ravin, H. Malech, and et al. Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire development J Allergy Clin Immunol 133 2014 1109 1115
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1109-1115
-
-
Yu, X.1
Almeida, J.R.2
Darko, S.3
Van Der Burg, M.4
Ravin, S.S.5
Malech, H.6
-
11
-
-
84896713795
-
Molecular and phenotypic abnormalities of B lymphocytes in patients with Wiskott-Aldrich syndrome
-
K. Simon, A.M. Anderson, E.K. Garabedian, D. Moratto, R.A. Sokolic, and F. Candotti Molecular and phenotypic abnormalities of B lymphocytes in patients with Wiskott-Aldrich syndrome J Allergy Clin Immunol 134 2014 896 899
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 896-899
-
-
Simon, K.1
Anderson, A.M.2
Garabedian, E.K.3
Moratto, D.4
Sokolic, R.A.5
Candotti, F.6
-
12
-
-
84903749842
-
The BLNK adaptor protein has a nonredundant role in human B-cell differentiation
-
C. Legresle-Peyrou, M. Millili, S. Luce, A. Boned, H. Sadek, J. Roullir, and et al. The BLNK adaptor protein has a nonredundant role in human B-cell differentiation J Allergy Clin Immunol 134 2014 145 154
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 145-154
-
-
Legresle-Peyrou, C.1
Millili, M.2
Luce, S.3
Boned, A.4
Sadek, H.5
Roullir, J.6
-
13
-
-
84897386968
-
Signaling lymphocyte activation molecule associated protein (SAP) pathway regulates human B cell tolerance
-
L. Menard, T. Caekert, N. Chamberlain, S.G. Tangye, S. Riminton, J.A. Church, and et al. Signaling lymphocyte activation molecule associated protein (SAP) pathway regulates human B cell tolerance J Allergy Clin Immunol 133 2014 1149 1161
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1149-1161
-
-
Menard, L.1
Caekert, T.2
Chamberlain, N.3
Tangye, S.G.4
Riminton, S.5
Church, J.A.6
-
14
-
-
84908440532
-
Dedicator of cytokinesis 8-deficient patients have a breakdown in peripheral B-cell tolerance and defective regulatory T cells
-
E. Janssen, H. Morbach, S. Ullas, J.M. Bannock, C. Massad, L. Menard, and 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 134 2014 1365 1374
-
(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
-
15
-
-
84905591094
-
Dysregulated extracellular signal-regulated kinase signaling associated with impaired B-cell receptor endocytosis in patients with common variable immunodeficiency
-
M. Visentine, R. Marrapodi, V. Conti, M. Mitrevski, A. Camponeschi, C. Lazzeri, and et al. Dysregulated extracellular signal-regulated kinase signaling associated with impaired B-cell receptor endocytosis in patients with common variable immunodeficiency J Allergy Clin Immunol 134 2014 401 410
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 401-410
-
-
Visentine, M.1
Marrapodi, R.2
Conti, V.3
Mitrevski, M.4
Camponeschi, A.5
Lazzeri, C.6
-
16
-
-
84897469677
-
A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
-
K. Pieper, M. Rizzi, M. Spelatas, C. Smulski, H. Sic, H. Kraus, and et al. A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency J Allergy Clin Immunol 133 2014 1222 1225
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1222-1225
-
-
Pieper, K.1
Rizzi, M.2
Spelatas, M.3
Smulski, C.4
Sic, H.5
Kraus, H.6
-
17
-
-
84899620518
-
Pulmonary alveolar proteinosis in adenosine-deaminase-deficient mice
-
R. Dhanju, W. Min, C. Ackerley, L. Cimpean, N. Palaniyar, C.M. Roifman, and et al. Pulmonary alveolar proteinosis in adenosine-deaminase-deficient mice J Allergy Clin Immunol 133 2014 1467 1471
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1467-1471
-
-
Dhanju, R.1
Min, W.2
Ackerley, C.3
Cimpean, L.4
Palaniyar, N.5
Roifman, C.M.6
-
18
-
-
84901804635
-
CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation
-
C.M. Buckner, S. Moir, L. Kardava, J. Ho, B.H. Santich, L.J. Kim, and et al. CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation J Allergy Clin Immunol 133 2014 1676 1685
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1676-1685
-
-
Buckner, C.M.1
Moir, S.2
Kardava, L.3
Ho, J.4
Santich, B.H.5
Kim, L.J.6
-
20
-
-
84891747684
-
Differential homeostatic dynamics of human regulatory T cell subsets following neonatal thymectomy
-
e1-6
-
A.W. Schadenberg, T. van den Broek, M.A. Siemelink, S.O. Algra, P.R. de Jong, N.J.G. Jansen, and et al. Differential homeostatic dynamics of human regulatory T cell subsets following neonatal thymectomy J Allergy Clin Immunol 133 2014 277 280 e1-6
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 277-280
-
-
Schadenberg, A.W.1
Van Den Broek, T.2
Siemelink, M.A.3
Algra, S.O.4
De Jong, P.R.5
Jansen, N.J.G.6
-
21
-
-
84903743112
-
APOe4 is associated with human enhanced in vivo innate immune responses in human subjects
-
S.C. Gale, L. Gao, C. Mikacenic, S.M. Coyle, N. Rafaels, T. Murray Dudenkov, and et al. APOe4 is associated with human enhanced in vivo innate immune responses in human subjects J Allergy Clin Immunol 134 2014 127 134
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 127-134
-
-
Gale, S.C.1
Gao, L.2
Mikacenic, C.3
Coyle, S.M.4
Rafaels, N.5
Murray Dudenkov, T.6
-
22
-
-
84901801796
-
Bruton's tyrosine kinase mediates TLR9-dependent human dendritic cell activation
-
V. Lougaris, M. Baronio, M. Vitali, G. Tampella, M. Cattalini, L. Tassone, and et al. Bruton's tyrosine kinase mediates TLR9-dependent human dendritic cell activation J Allergy Clin Immunol 133 2014 1644 1650
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1644-1650
-
-
Lougaris, V.1
Baronio, M.2
Vitali, M.3
Tampella, G.4
Cattalini, M.5
Tassone, L.6
-
23
-
-
84899618667
-
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment
-
Y. Zhang, X. Yu, M. Ichikawa, J.J. Lyons, S. Datta, I.T. Lamborn, H. Jing, and et al. Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment J Allergy Clin Immunol 133 2014 1400 1409
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1400-1409
-
-
Zhang, Y.1
Yu, X.2
Ichikawa, M.3
Lyons, J.J.4
Datta, S.5
Lamborn, I.T.6
Jing, H.7
-
24
-
-
84904036824
-
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia
-
A. Stray-Pedersen, P.H. Backe, H.S. Sorte, L. Mørkrid, N.Y. Chokshi, H.C. Erichsen, and et al. PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia Am J Hum Genet 95 2014 96 107
-
(2014)
Am J Hum Genet
, vol.95
, pp. 96-107
-
-
Stray-Pedersen, A.1
Backe, P.H.2
Sorte, H.S.3
Mørkrid, L.4
Chokshi, N.Y.5
Erichsen, H.C.6
-
25
-
-
84899629014
-
Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
-
A. Sassi, S. Lazaroski, G. Wu, S.M. Haslam, M. Fliegauf, F. Mellouli, and et al. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels J Allergy Clin Immunol 133 2014 1410 1419
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1410-1419
-
-
Sassi, A.1
Lazaroski, S.2
Wu, G.3
Haslam, S.M.4
Fliegauf, M.5
Mellouli, F.6
-
26
-
-
84901778963
-
Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency
-
E. Salzer, A. Kansu, H. Sic, P. Majek, A. Ikinciogullari, F.E. Dogu, and et al. Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency J Allergy Clin Immunol 133 2014 1651 1659.e12
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1651-1659e12
-
-
Salzer, E.1
Kansu, A.2
Sic, H.3
Majek, P.4
Ikinciogullari, A.5
Dogu, F.E.6
-
27
-
-
84938070889
-
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations
-
D. Schubert, C. Bode, R. Kenefeck, T.Z. Hou, J.B. Wing, A. Kennedy, and et al. Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations Nat Med 20 2014 1410 1416
-
(2014)
Nat Med
, vol.20
, pp. 1410-1416
-
-
Schubert, D.1
Bode, C.2
Kenefeck, R.3
Hou, T.Z.4
Wing, J.B.5
Kennedy, A.6
-
28
-
-
84907909000
-
Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4
-
H.S. Kuehn, W. Ouyang, B. Lo, E.K. Deenick, J.E. Niemela, D.T. Avery, and et al. Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4 Science 345 2014 1623 1627
-
(2014)
Science
, vol.345
, pp. 1623-1627
-
-
Kuehn, H.S.1
Ouyang, W.2
Lo, B.3
Deenick, E.K.4
Niemela, J.E.5
Avery, D.T.6
-
29
-
-
84907008346
-
A human immunodeficiency caused by mutations in the PIK3R1 gene
-
M.C. Deau, L. Heurtier, P. Frange, F. Suarez, C. Bole-Feysot, P. Nitschke, and et al. A human immunodeficiency caused by mutations in the PIK3R1 gene J Clin Invest 124 2014 3923 3928
-
(2014)
J Clin Invest
, vol.124
, pp. 3923-3928
-
-
Deau, M.C.1
Heurtier, L.2
Frange, P.3
Suarez, F.4
Bole-Feysot, C.5
Nitschke, P.6
-
30
-
-
84921847830
-
Heterozygous splice mutation in PIK3R1 causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K
-
C.L. Lucas, Y. Zhang, A. Venida, Y. Wang, J. Hughes, J. McElwee, and et al. Heterozygous splice mutation in PIK3R1 causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K J Exp Med 211 2014 2537 2547
-
(2014)
J Exp Med
, vol.211
, pp. 2537-2547
-
-
Lucas, C.L.1
Zhang, Y.2
Venida, A.3
Wang, Y.4
Hughes, J.5
McElwee, J.6
-
31
-
-
84923384476
-
Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity
-
K.L. Willmann, S. Klaver, F. Doʇu, E. Santos-Valente, W. Garncarz, I. Bilic, and et al. Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity Nat Commun 5 2014 5360
-
(2014)
Nat Commun
, vol.5
, pp. 5360
-
-
Willmann, K.L.1
Klaver, S.2
Doʇu, F.3
Santos-Valente, E.4
Garncarz, W.5
Bilic, I.6
-
32
-
-
84915745173
-
Inherited BCL10 deficiency impairs hematopoietic and nonhematopoietic immunity
-
J.M. Torres, R. Martinez-Barricarte, S. García-Gómez, M.S. Mazariegos, Y. Itan, B. Boisson, and et al. Inherited BCL10 deficiency impairs hematopoietic and nonhematopoietic immunity J Clin Invest 124 2014 5239 5248
-
(2014)
J Clin Invest
, vol.124
, pp. 5239-5248
-
-
Torres, J.M.1
Martinez-Barricarte, R.2
García-Gómez, S.3
Mazariegos, M.S.4
Itan, Y.5
Boisson, B.6
-
33
-
-
84902342846
-
CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation
-
E. Martin, N. Palmic, S. Sanquer, C. Lenoir, F. Hauck, C. Mongellaz, and et al. CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation Nature 510 2014 288 292
-
(2014)
Nature
, vol.510
, pp. 288-292
-
-
Martin, E.1
Palmic, N.2
Sanquer, S.3
Lenoir, C.4
Hauck, F.5
Mongellaz, C.6
-
34
-
-
84922393563
-
JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia
-
K. Boztug, P.M. Järvinen, E. Salzer, T. Racek, S. Mönch, W. Garncarz, and et al. JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia Nat Genet 46 2014 1021 1027
-
(2014)
Nat Genet
, vol.46
, pp. 1021-1027
-
-
Boztug, K.1
Järvinen, P.M.2
Salzer, E.3
Racek, T.4
Mönch, S.5
Garncarz, W.6
-
35
-
-
84905825645
-
Activated STING in a vascular and pulmonary syndrome
-
Y. Liu, A.A. Jesus, B. Marrero, D. Yang, S.E. Ramsey, G.A. Montealegre Sanchez, and et al. Activated STING in a vascular and pulmonary syndrome N Engl J Med 371 2014 507 518
-
(2014)
N Engl J Med
, vol.371
, pp. 507-518
-
-
Liu, Y.1
Jesus, A.A.2
Marrero, B.3
Yang, D.4
Ramsey, S.E.5
Montealegre Sanchez, G.A.6
-
36
-
-
84911922142
-
An inherited mutation in NLRC4 causes autoinflammation in human and mice
-
A. Kitamura, Y. Sasaki, T. Abe, H. Kano, and K. Yasutomo An inherited mutation in NLRC4 causes autoinflammation in human and mice J Exp Med 211 2014 2385 2396
-
(2014)
J Exp Med
, vol.211
, pp. 2385-2396
-
-
Kitamura, A.1
Sasaki, Y.2
Abe, T.3
Kano, H.4
Yasutomo, K.5
-
37
-
-
84922008927
-
Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation
-
N. Romberg, K. Al Moussawi, C. Nelson-Williams, A.L. Stiegler, E. Loring, M. Choi, and et al. Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation Nat Genet 46 2014 1135 1139
-
(2014)
Nat Genet
, vol.46
, pp. 1135-1139
-
-
Romberg, N.1
Al Moussawi, K.2
Nelson-Williams, C.3
Stiegler, A.L.4
Loring, E.5
Choi, M.6
-
38
-
-
84927126118
-
An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome
-
S.W. Canna, A.A. de Jesus, S. Gouni, S.R. Brooks, B. Marrero, Y. Liu, and et al. An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome Nat Genet 46 2014 1140 1146
-
(2014)
Nat Genet
, vol.46
, pp. 1140-1146
-
-
Canna, S.W.1
De Jesus, A.A.2
Gouni, S.3
Brooks, S.R.4
Marrero, B.5
Liu, Y.6
-
39
-
-
84895461649
-
Early-onset stroke and vasculopathy associated with mutations in ADA2
-
Q. Zhou, D. Yang, A.K. Ombrello, A.V. Zavialov, C. Toro, A.V. Zavialov, and et al. Early-onset stroke and vasculopathy associated with mutations in ADA2 N Engl J Med 370 2014 911 920
-
(2014)
N Engl J Med
, vol.370
, pp. 911-920
-
-
Zhou, Q.1
Yang, D.2
Ombrello, A.K.3
Zavialov, A.V.4
Toro, C.5
Zavialov, A.V.6
-
40
-
-
84895465707
-
Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy
-
P. Navon-Elkan, S.B. Pierce, R. Segel, T. Walsh, J. Barash, S. Padeh, and et al. Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy N Engl J Med 370 2014 921 931
-
(2014)
N Engl J Med
, vol.370
, pp. 921-931
-
-
Navon-Elkan, P.1
Pierce, S.B.2
Segel, R.3
Walsh, T.4
Barash, J.5
Padeh, S.6
-
42
-
-
84908584244
-
Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)
-
P.K. Chakraborty, K. Schmitz-Abe, E.K. Kennedy, H. Mamady, T. Naas, D. Durie, and et al. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) Blood 124 2014 2867 2871
-
(2014)
Blood
, vol.124
, pp. 2867-2871
-
-
Chakraborty, P.K.1
Schmitz-Abe, K.2
Kennedy, E.K.3
Mamady, H.4
Naas, T.5
Durie, D.6
-
43
-
-
84919599348
-
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome due to tetratricopeptide repeat domain 7A deficiency
-
R. Lemoine, J. Pachlopnik-Schmid, H.F. Farin, A. Bigorgne, M. Debre, M. Sepulveda, and et al. Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome due to tetratricopeptide repeat domain 7A deficiency J Allergy Clin Immunol 134 2014 1354 1364
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1354-1364
-
-
Lemoine, R.1
Pachlopnik-Schmid, J.2
Farin, H.F.3
Bigorgne, A.4
Debre, M.5
Sepulveda, M.6
-
44
-
-
84896729331
-
Fatal combined immunodeficiency associated with heterozygous mutation in STAT1
-
N. Sharfe, A. Nahum, A. Newell, H. Dadi, B. Ngan, S.L. Pereira, and et al. Fatal combined immunodeficiency associated with heterozygous mutation in STAT1 J Allergy Clin Immunol 133 2014 807 817
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 807-817
-
-
Sharfe, N.1
Nahum, A.2
Newell, A.3
Dadi, H.4
Ngan, B.5
Pereira, S.L.6
-
45
-
-
84909643087
-
Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100
-
C.E. Lee, D.A. Fulcher, B. Whittle, R. Chand, N. Fewings, M. Field, and et al. Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100 Blood 124 2014 2964 2972
-
(2014)
Blood
, vol.124
, pp. 2964-2972
-
-
Lee, C.E.1
Fulcher, D.A.2
Whittle, B.3
Chand, R.4
Fewings, N.5
Field, M.6
-
46
-
-
84901500584
-
Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKb
-
S.O. Burns, V. Plagnol, B.M. Gutierrez, D. Al-Zahrani, J. Curtis, M. Gaspar, and et al. Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKb J Allergy Clin Immunol 134 2014 215 218
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 215-218
-
-
Burns, S.O.1
Plagnol, V.2
Gutierrez, B.M.3
Al-Zahrani, D.4
Curtis, J.5
Gaspar, M.6
-
47
-
-
84914159176
-
Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers
-
C. Aguilar, C. Lenoir, N. Lambert, B. Begue, N. Brousse, D. Canioni, and et al. Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers J Allergy Clin Immunol 134 2014 1131 1142
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1131-1142
-
-
Aguilar, C.1
Lenoir, C.2
Lambert, N.3
Begue, B.4
Brousse, N.5
Canioni, D.6
-
48
-
-
84897412977
-
Kindlin 3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III
-
E. van de Vijver, A.T. Tool, O. Sanal, M. Cetin, S. Unal, S. Aytac, and et al. Kindlin 3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III J Allergy Clin Immunol 133 2014 1215 1218
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1215-1218
-
-
Van De Vijver, E.1
Tool, A.T.2
Sanal, O.3
Cetin, M.4
Unal, S.5
Aytac, S.6
-
49
-
-
84897396302
-
Vaccine strain varicella-zoster virus-induced central nervous system vasculopathy as the presenting feature of DOCK8 deficiency
-
A. Sabry, P.J. Hauk, H. Jing, H.C. Su, N.V. Stence, D.M. Mirsky, and et al. Vaccine strain varicella-zoster virus-induced central nervous system vasculopathy as the presenting feature of DOCK8 deficiency J Allergy Clin Immunol 133 2014 1225 1227
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1225-1227
-
-
Sabry, A.1
Hauk, P.J.2
Jing, H.3
Su, H.C.4
Stence, N.V.5
Mirsky, D.M.6
-
50
-
-
84903708186
-
Presence of hypogammaglobulinemia and abnormal antibody responses in GATA2 deficiency
-
J. Chou, M. Lutskiy, E. Tsitsikov, L.D. Notarangelo, R.S. Geha, and A. Dioun Presence of hypogammaglobulinemia and abnormal antibody responses in GATA2 deficiency J Allergy Clin Immunol 134 2014 223 226
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 223-226
-
-
Chou, J.1
Lutskiy, M.2
Tsitsikov, E.3
Notarangelo, L.D.4
Geha, R.S.5
Dioun, A.6
-
52
-
-
84904872011
-
Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia
-
N.K. Serwas, D. Cagdas, S.A. Ban, K. Bienemann, E. Salzer, I. Tezcan, and et al. Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia Blood 124 2014 655 657
-
(2014)
Blood
, vol.124
, pp. 655-657
-
-
Serwas, N.K.1
Cagdas, D.2
Ban, S.A.3
Bienemann, K.4
Salzer, E.5
Tezcan, I.6
-
53
-
-
84891030577
-
Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency
-
C.L. Lucas, H.S. Kuehn, F. Zhao, J.E. Niemela, E.K. Deenick, U. Palendira, and et al. Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency Nat Immunol 15 2014 88 97
-
(2014)
Nat Immunol
, vol.15
, pp. 88-97
-
-
Lucas, C.L.1
Kuehn, H.S.2
Zhao, F.3
Niemela, J.E.4
Deenick, E.K.5
Palendira, U.6
-
54
-
-
84908147862
-
Lessons in gene hunting: A RAG1 mutation presenting with agammaglobulinemia and absence of B cells
-
M. Hadayat, M.J. Masaad, N.Y. Lee, M.E. Conley, J.S. Orange, T.K. Ohsumi, and et al. Lessons in gene hunting: a RAG1 mutation presenting with agammaglobulinemia and absence of B cells J Allergy Clin Immunol 134 2014 983 985
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 983-985
-
-
Hadayat, M.1
Masaad, M.J.2
Lee, N.Y.3
Conley, M.E.4
Orange, J.S.5
Ohsumi, T.K.6
-
55
-
-
84896710741
-
Autoimmunity due to RAG deficiency and estimated disease incidence in RAG1/2 mutations
-
K. Chen, W. Wu, D. Mathew, Y. Zhang, S.K. Browne, L.B. Rosen, and et al. Autoimmunity due to RAG deficiency and estimated disease incidence in RAG1/2 mutations J Allergy Clin Immunol 134 2014 880 882
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 880-882
-
-
Chen, K.1
Wu, W.2
Mathew, D.3
Zhang, Y.4
Browne, S.K.5
Rosen, L.B.6
-
56
-
-
84919843125
-
A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency
-
H. Abolhassani, N. Wang, A. Aghamohammadi, N. Rezaei, Y.N. Lee, F. Frugoni, and et al. A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency J Allergy Clin Immunol 134 2014 1375 1380
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1375-1380
-
-
Abolhassani, H.1
Wang, N.2
Aghamohammadi, A.3
Rezaei, N.4
Lee, Y.N.5
Frugoni, F.6
-
57
-
-
84897448055
-
Lesson from hypomorphic recombinant activating gene (RAG) mutations: Why asymptomatic siblings should be tested
-
C. Schuetz, U. Pannicke, E.M. Jacobsen, S. Burggraf, M.H. Albert, M. Honig, and et al. Lesson from hypomorphic recombinant activating gene (RAG) mutations: why asymptomatic siblings should be tested J Allergy Clin Immunol 133 2014 1211 1215
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1211-1215
-
-
Schuetz, C.1
Pannicke, U.2
Jacobsen, E.M.3
Burggraf, S.4
Albert, M.H.5
Honig, M.6
-
58
-
-
84897389616
-
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency
-
Y.N. Lee, F. Frugoni, K. Dobbs, J.E. Walter, S. Giliani, A.R. Gennery, and et al. A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency J Allergy Clin Immunol 133 2014 1099 1108
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1099-1108
-
-
Lee, Y.N.1
Frugoni, F.2
Dobbs, K.3
Walter, J.E.4
Giliani, S.5
Gennery, A.R.6
-
59
-
-
84897444766
-
Similar recombination-activating gene (RAG) mutation result in similar immunological effects but in different clinical phenotypes
-
H. IJspeert, G.J. Driessen, M.J. Moorhouse, N.G. Hartwig, B. Wolska-Kunierz, K. Kalwak, and et al. Similar recombination-activating gene (RAG) mutation result in similar immunological effects but in different clinical phenotypes J Allergy Clin Immunol 133 2014 1124 1133
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1124-1133
-
-
Ijspeert, H.1
Driessen, G.J.2
Moorhouse, M.J.3
Hartwig, N.G.4
Wolska-Kunierz, B.5
Kalwak, K.6
-
60
-
-
84905502530
-
Gene hunting in the genomic era: Approaches to diagnostic dilemmas in patients with primary immunodeficiencies
-
C. Platt, R.S. Geha, and J. Chou Gene hunting in the genomic era: approaches to diagnostic dilemmas in patients with primary immunodeficiencies J Allergy Clin Immunol 134 2014 262 268
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 262-268
-
-
Platt, C.1
Geha, R.S.2
Chou, J.3
-
61
-
-
84895064425
-
Targeted next generation sequencing: A novel diagnostic tool for primary immunodeficiencies
-
I.J. Nijman, J.M. van Montfran, M. Hoogstraat, M.L. Boes, L. van de Corput, L.D. Renner, and et al. Targeted next generation sequencing: A novel diagnostic tool for primary immunodeficiencies J Allergy Clin Immunol 133 2014 529 534
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 529-534
-
-
Nijman, I.J.1
Van Montfran, J.M.2
Hoogstraat, M.3
Boes, M.L.4
Van De Corput, L.5
Renner, L.D.6
-
62
-
-
84919841275
-
Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis
-
R. Meazza, C. Tuberosa, V. Cetica, M. Falco, S. Parolini, S. Grieve, and et al. Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis J Allergy Clin Immunol 134 2014 1381 1387
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1381-1387
-
-
Meazza, R.1
Tuberosa, C.2
Cetica, V.3
Falco, M.4
Parolini, S.5
Grieve, S.6
-
63
-
-
84903751001
-
Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency
-
S.Y. Pai, H. de Boer, M.J. Masaad, T.A. Chatila, S. Keles, H.H. Jabara, and et al. Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency J Allergy Clin Immunol 134 2014 221 223
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 221-223
-
-
Pai, S.Y.1
De Boer, H.2
Masaad, M.J.3
Chatila, T.A.4
Keles, S.5
Jabara, H.H.6
-
64
-
-
85027940542
-
Inflammatory manifestations in a single-center cohort of patients with chronic granulomatous disease
-
A. Magnani, P. Brosselin, J. Beaute, N. de Vergnes, R. Mouy, M. Debre, and et al. Inflammatory manifestations in a single-center cohort of patients with chronic granulomatous disease J Allergy Clin Immunol 134 2014 655 662.e8
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 655-662e8
-
-
Magnani, A.1
Brosselin, P.2
Beaute, J.3
De Vergnes, N.4
Mouy, R.5
Debre, M.6
-
65
-
-
84903740988
-
Clinical picture and treatment of 2212 patients with common variable immunodeficiency
-
B. Gathmann, N. Mahlaoui, L. Gerard, E. Oksenhendler, K. Warnat, I. Schulze, and et al. Clinical picture and treatment of 2212 patients with common variable immunodeficiency J Allergy Clin Immunol 134 2014 116 126
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 116-126
-
-
Gathmann, B.1
Mahlaoui, N.2
Gerard, L.3
Oksenhendler, E.4
Warnat, K.5
Schulze, I.6
-
66
-
-
84899622887
-
Common variable immunodeficiency is associated with a functional deficiency of invariant natural killer cells
-
Y. Gao, S. Workmann, S. Gadola, T. Elliott, B. Grimbacher, and A.P. Williams Common variable immunodeficiency is associated with a functional deficiency of invariant natural killer cells J Allergy Clin Immunol 134 2014 1420 1428
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1420-1428
-
-
Gao, Y.1
Workmann, S.2
Gadola, S.3
Elliott, T.4
Grimbacher, B.5
Williams, A.P.6
-
67
-
-
84895064377
-
Tertiary lymphoid neogenesis is a component of pulmonary lymphoid hyperplasia in patients with common variable immunodeficiency
-
P.J. Maglione, H.M. Ko, M.B. Beasley, J.A. Strauchen, and C. Cunningham-Rundles Tertiary lymphoid neogenesis is a component of pulmonary lymphoid hyperplasia in patients with common variable immunodeficiency J Allergy Clin Immunol 134 2014 535 542
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 535-542
-
-
Maglione, P.J.1
Ko, H.M.2
Beasley, M.B.3
Strauchen, J.A.4
Cunningham-Rundles, C.5
-
68
-
-
84903746318
-
Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome
-
S. Kracker, J. Curtis, M.A. Ibrahim, A. Sediva, J. Salisbury, V. Campr, and et al. Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome J Allergy Clin Immunol 134 2014 233 236
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 233-236
-
-
Kracker, S.1
Curtis, J.2
Ibrahim, M.A.3
Sediva, A.4
Salisbury, J.5
Campr, V.6
-
69
-
-
84895056711
-
A novel mutation in IFN-g receptor 1 presenting as multisystem Mycobacteium intracellulare infection
-
D.M. Rose, J. Atkins, S.M. Holland, and A.J. Infante A novel mutation in IFN-g receptor 1 presenting as multisystem Mycobacteium intracellulare infection J Allergy Clin Immunol 134 2014 591 592
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 591-592
-
-
Rose, D.M.1
Atkins, J.2
Holland, S.M.3
Infante, A.J.4
-
70
-
-
84901777686
-
Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype
-
H. Jing, Q. Zhang, Y. Zhang, B.J. Hill, C.G. Dove, E.W. Gelfand, and et al. Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype J Allergy Clin Immunol 133 2014 1667 1675
-
(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
-
71
-
-
84903692809
-
A case of partial dedicators of cytokinesis 8 deficiency with altered effector phenotype and impaired CD8+ and natural killer cytotoxicity
-
R. Ruiz-Garcia, S. Lermo-Rojo, L. Martinez-Lostao, E. Mancebo, S. Mora-Diaz, S. Paz-Artal, and et al. A case of partial dedicators of cytokinesis 8 deficiency with altered effector phenotype and impaired CD8+ and natural killer cytotoxicity J Allergy Clin Immunol 134 2014 218 221
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 218-221
-
-
Ruiz-Garcia, R.1
Lermo-Rojo, S.2
Martinez-Lostao, L.3
Mancebo, E.4
Mora-Diaz, S.5
Paz-Artal, S.6
-
72
-
-
84914151539
-
Gain of function mutations in signal transducer and activator of transcription 1 (STAT1): Chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding
-
G. Frans, L. Moens, H. Schaballie, L. Van Eyck, H. Borgers, M. Wayts, and et al. Gain of function mutations in signal transducer and activator of transcription 1 (STAT1): chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding J Allergy Clin Immunol 134 2014 1209 1212
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1209-1212
-
-
Frans, G.1
Moens, L.2
Schaballie, H.3
Van Eyck, L.4
Borgers, H.5
Wayts, M.6
-
73
-
-
84896709292
-
Penicillium marneffei infection and impaired IFNγ immunity in humans with autosomal-dominant gain of phosphorylation STAT1 mutations
-
P.P.W. Lee, H. Mao, W. Yang, K.W. Can, M.H. Ko, J.F. Chan, and et al. Penicillium marneffei infection and impaired IFNγ immunity in humans with autosomal-dominant gain of phosphorylation STAT1 mutations J Allergy Clin Immunol 134 2014 894 896.e5
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 894-896e5
-
-
Lee, P.P.W.1
Mao, H.2
Yang, W.3
Can, K.W.4
Ko, M.H.5
Chan, J.F.6
-
74
-
-
84903734036
-
Gain of function signal transducer and activator of transcription 1 (STAT1) mutation-related primary immunodeficiency is associated with disseminated mucormycosis
-
N. Kumar, M.E. Hanks, P. Chandrasekan, B.C. Davis, A.P. Hsu, N.J. Van Wagoner, and et al. Gain of function signal transducer and activator of transcription 1 (STAT1) mutation-related primary immunodeficiency is associated with disseminated mucormycosis J Allergy Clin Immunol 134 2014 236 239
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 236-239
-
-
Kumar, N.1
Hanks, M.E.2
Chandrasekan, P.3
Davis, B.C.4
Hsu, A.P.5
Van Wagoner, N.J.6
-
75
-
-
84896722382
-
CARD9 mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficiency
-
X. Wang, W. Wang, Z. Lin, X. Wang, T. Li, J. Yu, and et al. CARD9 mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficiency J Allergy Clin Immunol 133 2014 905 908
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 905-908
-
-
Wang, X.1
Wang, W.2
Lin, Z.3
Wang, X.4
Li, T.5
Yu, J.6
-
76
-
-
84906543118
-
Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States
-
A. Kwan, R.S. Abraham, R. Currier, A. Brower, K. Andruszewski, J.K. Abbott, and et al. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States JAMA 312 2014 729 738
-
(2014)
JAMA
, vol.312
, pp. 729-738
-
-
Kwan, A.1
Abraham, R.S.2
Currier, R.3
Brower, A.4
Andruszewski, K.5
Abbott, J.K.6
-
77
-
-
84903705060
-
Diagnosis of immunodeficiency phosphorylase defect by using tandem mass spectrometry in dried blood spots
-
G. La Marca, C. Canessa, E. Giocaliere, F. Romano, S. Malvagia, S. Funghini, and et al. Diagnosis of immunodeficiency phosphorylase defect by using tandem mass spectrometry in dried blood spots J Allergy Clin Immunol 134 2014 155 159
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 155-159
-
-
La Marca, G.1
Canessa, C.2
Giocaliere, E.3
Romano, F.4
Malvagia, S.5
Funghini, S.6
-
78
-
-
84903731039
-
Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B cell immunodeficiencies
-
S. Borte, M. Meeths, I. Liebschert, K. Krist, M. Norsdenkjold, L. Hammarstrom, and et al. Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B cell immunodeficiencies J Allergy Clin Immunol 134 2014 226 228
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 226-228
-
-
Borte, S.1
Meeths, M.2
Liebschert, I.3
Krist, K.4
Norsdenkjold, M.5
Hammarstrom, L.6
-
79
-
-
84906825678
-
Control lymphocyte subset: Can one country's values serve for another's?
-
W.L. Mandala, J. Anaworanich, T. Aporapong, S.J. Kerr, J.M. MacLennan, C. Hanson, and et al. Control lymphocyte subset: can one country's values serve for another's? J Allergy Clin Immunol 134 2014 759 761
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 759-761
-
-
Mandala, W.L.1
Anaworanich, J.2
Aporapong, T.3
Kerr, S.J.4
MacLennan, J.M.5
Hanson, C.6
-
80
-
-
84895059316
-
Primary Immune Deficiency Treatment Consortium (PIDTC) report
-
L.M. Griffiths, M.J. Cowan, L.D. Notarangelo, D.B. Kohn, J.M. Puck, S.Y. Pai, and et al. Primary Immune Deficiency Treatment Consortium (PIDTC) report J Allergy Clin Immunol 133 2014 335 347
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 335-347
-
-
Griffiths, L.M.1
Cowan, M.J.2
Notarangelo, L.D.3
Kohn, D.B.4
Puck, J.M.5
Pai, S.Y.6
-
81
-
-
84897417058
-
Establishing diagnostic criteria for severe combined immunodeficiency (SCID), leaky SCID and Omenn syndrome: The Primary Immune Deficiency Treatment Consortium experience
-
W.T. Shearer, E. Dunn, L.D. Notarangelo, C.C. Dvorak, J.M. Puck, B.R. Logan, and et al. Establishing diagnostic criteria for severe combined immunodeficiency (SCID), leaky SCID and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience J Clin Allergy Immunol 133 2014 1092 1098
-
(2014)
J Clin Allergy Immunol
, vol.133
, pp. 1092-1098
-
-
Shearer, W.T.1
Dunn, E.2
Notarangelo, L.D.3
Dvorak, C.C.4
Puck, J.M.5
Logan, B.R.6
-
82
-
-
84895062421
-
Survey on retransplantation criteria for patients with severe combined immunodeficiency
-
E. Haddad, Z. Allakverdi, L.M. Griffiths, M.J. Cowan, and L.D. Notarangelo Survey on retransplantation criteria for patients with severe combined immunodeficiency J Allergy Clin Immunol 133 2014 597 599
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 597-599
-
-
Haddad, E.1
Allakverdi, Z.2
Griffiths, L.M.3
Cowan, M.J.4
Notarangelo, L.D.5
-
83
-
-
84908123060
-
Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency
-
C.C. Dvorak, A. Hassan, M.A. Slatter, M. Honig, A.C. Lankester, R.H. Buckley, and et al. Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency J Allergy Clin Immunol 134 2014 935 943
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 935-943
-
-
Dvorak, C.C.1
Hassan, A.2
Slatter, M.A.3
Honig, M.4
Lankester, A.C.5
Buckley, R.H.6
-
84
-
-
84904876386
-
Transplantation outcomes for severe combined immunodeficiency, 2000-2009
-
S.Y. Pai, B.R. Logan, L.M. Griffith, R.H. Buckley, R.E. Parrott, C.C. Dvorak, and et al. Transplantation outcomes for severe combined immunodeficiency, 2000-2009 N Engl J Med 371 2014 434 446
-
(2014)
N Engl J Med
, vol.371
, pp. 434-446
-
-
Pai, S.Y.1
Logan, B.R.2
Griffith, L.M.3
Buckley, R.H.4
Parrott, R.E.5
Dvorak, C.C.6
-
85
-
-
84901804522
-
Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency
-
A. Hassan, P. Lee, P. Maggina, J.H. Xu, D. Moreira, M. Slatter, and et al. Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency J Allergy Clin Immunol 133 2014 1660 1666
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1660-1666
-
-
Hassan, A.1
Lee, P.2
Maggina, P.3
Xu, J.H.4
Moreira, D.5
Slatter, M.6
-
86
-
-
84919640076
-
Severe cutaneous human papilloma virus infection associated with natural killer deficiency following stem cell transplantation for severe combined immunodeficiency
-
Q.U. Kamili, F.O. Seeborg, K. Saxena, S.K. Nicholas, P.P. Banerjee, L.S. Angelo, and et al. Severe cutaneous human papilloma virus infection associated with natural killer deficiency following stem cell transplantation for severe combined immunodeficiency J Allergy Clin Immunol 134 2014 1451 1453.e1
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1451-1453e1
-
-
Kamili, Q.U.1
Seeborg, F.O.2
Saxena, K.3
Nicholas, S.K.4
Banerjee, P.P.5
Angelo, L.S.6
-
87
-
-
84892636089
-
SCID patients with ARTEMIS vs RAG deficiencies following HCT: Increased risk of late toxicity in ARTEMIS-deficient SCID
-
C. Schuetz, B. Neven, C.C. Dvorak, S. Leroy, M.J. Ege, U. Pannicke, and et al. SCID patients with ARTEMIS vs RAG deficiencies following HCT: increased risk of late toxicity in ARTEMIS-deficient SCID Blood 123 2014 281 289
-
(2014)
Blood
, vol.123
, pp. 281-289
-
-
Schuetz, C.1
Neven, B.2
Dvorak, C.C.3
Leroy, S.4
Ege, M.J.5
Pannicke, U.6
-
88
-
-
84914102333
-
Haploidential T-cell alpha beta receptor and CD19-depleted stem cell transplant for Wiskott Aldrich syndrome
-
G. Kharya, Z. Nademi, T.R. Leahy, J. Dunn, D. Barge, and A. Shulz Haploidential T-cell alpha beta receptor and CD19-depleted stem cell transplant for Wiskott Aldrich syndrome J Allergy Clin Immunol 134 2014 1199 1201
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1199-1201
-
-
Kharya, G.1
Nademi, Z.2
Leahy, T.R.3
Dunn, J.4
Barge, D.5
Shulz, A.6
-
89
-
-
84914160574
-
Circulating endothelial cells as markers of endothelial dysfunction during hematopoietic stem cell transplantation for pediatric primary immunodeficiency
-
F. Touzot, D. Moshous, G. Cros, P. Frange, M. Chornton, M.L. Friedmind, and et al. Circulating endothelial cells as markers of endothelial dysfunction during hematopoietic stem cell transplantation for pediatric primary immunodeficiency J Allergy Clin Immunol 134 2014 1203 1206
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1203-1206
-
-
Touzot, F.1
Moshous, D.2
Cros, G.3
Frange, P.4
Chornton, M.5
Friedmind, M.L.6
-
90
-
-
84896738619
-
B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients
-
I. Brigida, A.V. Sauer, F. Ferrua, S. Giannelli, S. Scaramuzza, V. Pistoia, and et al. B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients J Allergy Clin Immunol 133 2014 799 806
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 799-806
-
-
Brigida, I.1
Sauer, A.V.2
Ferrua, F.3
Giannelli, S.4
Scaramuzza, S.5
Pistoia, V.6
-
91
-
-
84897389322
-
Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome
-
N.P. Van Til, R. Sarwari, T.P. Visser, J. Hauer, C. Lagresle-Peyrou, G. van der Velden, and et al. Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome J Allergy Clin Immunol 133 2014 1116 1123
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1116-1123
-
-
Van Til, N.P.1
Sarwari, R.2
Visser, T.P.3
Hauer, J.4
Lagresle-Peyrou, C.5
Van Der Velden, G.6
-
92
-
-
84907880404
-
A modified γ-retrovirus vector for X-linked severe combined immunodeficiency
-
S. Hacein-Bey-Abina, S.Y. Pai, H.B. Gaspar, M. Armant, C.C. Berry, S. Blanche, and et al. A modified γ-retrovirus vector for X-linked severe combined immunodeficiency N Engl J Med 371 2014 1407 1417
-
(2014)
N Engl J Med
, vol.371
, pp. 1407-1417
-
-
Hacein-Bey-Abina, S.1
Pai, S.Y.2
Gaspar, H.B.3
Armant, M.4
Berry, C.C.5
Blanche, S.6
-
93
-
-
84891735723
-
Intravenous immunoglobulin induces a functional silencing program similar to anergy in human B cells
-
J.F. Seite, C. Goutsmedt, P. Younoi, J.O. Pers, and S. Hillion Intravenous immunoglobulin induces a functional silencing program similar to anergy in human B cells J Allergy Clin Immunol 133 2014 181 188
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 181-188
-
-
Seite, J.F.1
Goutsmedt, C.2
Younoi, P.3
Pers, J.O.4
Hillion, S.5
-
94
-
-
84896692591
-
Dendritic cell immunoreceptor: A novel receptor for intravenous immunoglobulin mediates induction of regulatory T cells
-
A.H. Massoud, M. Yona, D. Xue, F. Chouiali, H. Alturaihi, A. Ablona, and et al. Dendritic cell immunoreceptor: a novel receptor for intravenous immunoglobulin mediates induction of regulatory T cells J Allergy Clin Immunol 133 2014 853 863
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 853-863
-
-
Massoud, A.H.1
Yona, M.2
Xue, D.3
Chouiali, F.4
Alturaihi, H.5
Ablona, A.6
-
95
-
-
84897458695
-
Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts
-
W.T. Shearer, T.A. Fleisher, R.H. Buckley, Z. Ballas, M. Ballow, M. Blaese, and et al. Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts J Allergy Clin Immunol 133 2014 961 966
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 961-966
-
-
Shearer, W.T.1
Fleisher, T.A.2
Buckley, R.H.3
Ballas, Z.4
Ballow, M.5
Blaese, M.6
-
96
-
-
84897136937
-
BCG vaccination in patients with severe combined immunodeficiency: Complications, risks and vaccination policies
-
B.E. Marciano, C.Y. Huang, G. Joshi, N. Rezaei, B. Costa Carvalho, Z. Allwood, and et al. BCG vaccination in patients with severe combined immunodeficiency: complications, risks and vaccination policies J Allergy Clin Immunol 133 2014 1134 1141
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1134-1141
-
-
Marciano, B.E.1
Huang, C.Y.2
Joshi, G.3
Rezaei, N.4
Costa Carvalho, B.5
Allwood, Z.6
-
97
-
-
84899645392
-
Beneficial IFN-α treatment of tumorous blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency
-
C. Papan, B. Hagel, V. Heinz, M.H. Albert, O. Ebert, J. Savalle-Belhoradsky, and et al. Beneficial IFN-α treatment of tumorous blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency J Allergy Clin Immunol 133 2014 1456 1458
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 1456-1458
-
-
Papan, C.1
Hagel, B.2
Heinz, V.3
Albert, M.H.4
Ebert, O.5
Savalle-Belhoradsky, J.6
-
98
-
-
84901807538
-
Plasmacytoid dendritic cell depletion in DOCK8 deficiency: Rescue of severe herpetic infections with IFN-α2b therapy
-
S. Keles, H.H. Jabara, I. Reisli, D.R. McDonald, I. Barlan, R. Hann-Wakim, and et al. Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-α2b therapy J Allergy Clin Immunol 133 2014 1753 1755
-
(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
Hann-Wakim, R.6
-
99
-
-
84914155258
-
Neutrophils in antiretroviral therapy controlled HIV demonstrate hyperactivation associated with a specific IL-17/IL-22 environment
-
L. Campillo-Gimenez, S. Casulli, Y. Dudoit, S. Seang, G. Carcelain, S. Lambert-Niclot, and et al. Neutrophils in antiretroviral therapy controlled HIV demonstrate hyperactivation associated with a specific IL-17/IL-22 environment J Allergy Clin Immunol 134 2014 1142 1152
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 1142-1152
-
-
Campillo-Gimenez, L.1
Casulli, S.2
Dudoit, Y.3
Seang, S.4
Carcelain, G.5
Lambert-Niclot, S.6
-
100
-
-
84895057775
-
Premature immune senescence during HIV-1 vertical infection relates with response to influenza vaccination
-
A. Cagigi, S. Rinaldi, A. Di Martino, E.C. Manno, P. Zangari, A. Aquilani, and et al. Premature immune senescence during HIV-1 vertical infection relates with response to influenza vaccination J Allergy Clin Immunol 133 2014 592 594
-
(2014)
J Allergy Clin Immunol
, vol.133
, pp. 592-594
-
-
Cagigi, A.1
Rinaldi, S.2
Di Martino, A.3
Manno, E.C.4
Zangari, P.5
Aquilani, A.6
-
101
-
-
84903610913
-
Progress in HIV-1 vaccine development
-
B.F. Haynes, M.A. Moody, M. Alam, M. Bonsignori, L. Verkoczy, G. Ferrari, and et al. Progress in HIV-1 vaccine development J Allergy Clin Immunol 134 2014 3 10
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 3-10
-
-
Haynes, B.F.1
Moody, M.A.2
Alam, M.3
Bonsignori, M.4
Verkoczy, L.5
Ferrari, G.6
-
102
-
-
84903615913
-
Recent developments in the search for a cure for HIV-1 infection: Targeting the latent reservoir for HIV-1
-
J.D. Siciliano, and R.F. Siciliano Recent developments in the search for a cure for HIV-1 infection: targeting the latent reservoir for HIV-1 J Allergy Clin Immunol 134 2014 12 19
-
(2014)
J Allergy Clin Immunol
, vol.134
, pp. 12-19
-
-
Siciliano, J.D.1
Siciliano, R.F.2
|