-
1
-
-
42049086504
-
Hemophagocytic lymphohistiocytosis and other hemophagocytic disorders
-
viii
-
A.H. Filipovich 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
-
2
-
-
33845619137
-
HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
-
J.I. Henter, A. Horne, M. Aricó, R.M. Egeler, A.H. Filipovich, and S. Imashuku HLH-2004: diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis Pediatr Blood Cancer 48 2007 124 131
-
(2007)
Pediatr Blood Cancer
, vol.48
, pp. 124-131
-
-
Henter, J.I.1
Horne, A.2
Aricó, M.3
Egeler, R.M.4
Filipovich, A.H.5
Imashuku, S.6
-
3
-
-
50249184550
-
Formation and function of the lytic NK-cell immunological synapse
-
J.S. Orange Formation and function of the lytic NK-cell immunological synapse Nat Rev Immunol 8 2008 713 725
-
(2008)
Nat Rev Immunol
, vol.8
, pp. 713-725
-
-
Orange, J.S.1
-
4
-
-
70350500464
-
Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11
-
U. zur Stadt, J. Rohr, W. Seifert, F. Koch, S. Grieve, and J. Pagel Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11 Am J Hum Genet 85 2009 482 492
-
(2009)
Am J Hum Genet
, vol.85
, pp. 482-492
-
-
Zur Stadt, U.1
Rohr, J.2
Seifert, W.3
Koch, F.4
Grieve, S.5
Pagel, J.6
-
5
-
-
29944442846
-
Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: Molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A
-
U. Zur Stadt, K. Beutel, S. Kolberg, R. Schneppenheim, H. Kabisch, and G. Janka Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A Hum Mutat 27 2006 62 68
-
(2006)
Hum Mutat
, vol.27
, pp. 62-68
-
-
Zur Stadt, U.1
Beutel, K.2
Kolberg, S.3
Schneppenheim, R.4
Kabisch, H.5
Janka, G.6
-
6
-
-
72849125357
-
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells
-
M. Côte, M.M. Ménager, A. Burgess, N. Mahlaoui, C. Picard, and C. Schaffner Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells J Clin Invest 119 2009 3765 3773
-
(2009)
J Clin Invest
, vol.119
, pp. 3765-3773
-
-
Côte, M.1
Ménager, M.M.2
Burgess, A.3
Mahlaoui, N.4
Picard, C.5
Schaffner, C.6
-
7
-
-
77957954413
-
Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2
-
M. Meeths, M. Entesarian, W. Al-Herz, S.C. Chiang, S.M. Wood, and W. Al-Ateeqi Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2 Blood 116 2010 2635 2643
-
(2010)
Blood
, vol.116
, pp. 2635-2643
-
-
Meeths, M.1
Entesarian, M.2
Al-Herz, W.3
Chiang, S.C.4
Wood, S.M.5
Al-Ateeqi, W.6
-
8
-
-
77956109360
-
STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5
-
V. Cetica, A. Santoro, K.C. Gilmour, E. Sieni, K. Beutel, and D. Pende STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5 J Med Genet 47 2010 595 600
-
(2010)
J Med Genet
, vol.47
, pp. 595-600
-
-
Cetica, V.1
Santoro, A.2
Gilmour, K.C.3
Sieni, E.4
Beutel, K.5
Pende, D.6
-
9
-
-
79953331939
-
IL-2 induces a WAVE2-dependent pathway for actin reorganization that enables WASp-independent human NK cell function
-
J.S. Orange, S. Roy-Ghanta, E.M. Mace, S. Maru, G.D. Rak, and K.B. Sanborn IL-2 induces a WAVE2-dependent pathway for actin reorganization that enables WASp-independent human NK cell function J Clin Invest 121 2011 1535 1548
-
(2011)
J Clin Invest
, vol.121
, pp. 1535-1548
-
-
Orange, J.S.1
Roy-Ghanta, S.2
MacE, E.M.3
Maru, S.4
Rak, G.D.5
Sanborn, K.B.6
|