-
1
-
-
20944449435
-
Genetic subtypes of familial hemophagocytic lymphohistiocytosis: Correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions
-
Ishii E, Ueda I, Shirakawa R, et al. Genetic subtypes of familial hemophagocytic lymphohistiocytosis: Correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions. Blood 2005;105:3442-3448.
-
(2005)
Blood
, vol.105
, pp. 3442-3448
-
-
Ishii, E.1
Ueda, I.2
Shirakawa, R.3
-
2
-
-
20144363940
-
Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
-
zur Stadt U, Schmidt S, Kasper B, et al. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11. Hum Mol Genet 2005;14:827-834.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 827-834
-
-
zur Stadt, U.1
Schmidt, S.2
Kasper, B.3
-
3
-
-
0036786375
-
Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation
-
Henter JI, Samuelsson-Horne A, Arico M, et al. Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation. Blood 2002;100:2367-2373.
-
(2002)
Blood
, vol.100
, pp. 2367-2373
-
-
Henter, J.I.1
Samuelsson-Horne, A.2
Arico, M.3
-
4
-
-
0020578818
-
Familial hemophagocytic lymphohistiocytosis
-
Janka GE. Familial hemophagocytic lymphohistiocytosis. Eur J Pediatr 1983;140:221-230.
-
(1983)
Eur J Pediatr
, vol.140
, pp. 221-230
-
-
Janka, G.E.1
-
5
-
-
0029879812
-
Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry
-
Arico M, Janka G, Fischer A, et al. Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. Leukemia 1996;10:197-203.
-
(1996)
Leukemia
, vol.10
, pp. 197-203
-
-
Arico, M.1
Janka, G.2
Fischer, A.3
-
6
-
-
0030943203
-
Frequency and severity of central nervous system lesions in hemophagocytic lymphohistiocytosis
-
Haddad E, Sulis ML, Jabado N, et al. Frequency and severity of central nervous system lesions in hemophagocytic lymphohistiocytosis. Blood 1997;89:794-800.
-
(1997)
Blood
, vol.89
, pp. 794-800
-
-
Haddad, E.1
Sulis, M.L.2
Jabado, N.3
-
7
-
-
0031927821
-
Familial hemophagocytic lymphohistiocytosis: Improved neurodevelopmental outcome after bone marrow transplantation
-
Shuper A, Attias D, Kornreich L, et al. Familial hemophagocytic lymphohistiocytosis: Improved neurodevelopmental outcome after bone marrow transplantation. J Pediatr 1998;133:126-128.
-
(1998)
J Pediatr
, vol.133
, pp. 126-128
-
-
Shuper, A.1
Attias, D.2
Kornreich, L.3
-
8
-
-
0036604376
-
Low natural killer activity and central nervous system disease as a high-risk prognostic indicator in young patients with hemophagocytic lymphohistiocytosis
-
Imashuku S, Hyakuna N, Funabiki T, et al. Low natural killer activity and central nervous system disease as a high-risk prognostic indicator in young patients with hemophagocytic lymphohistiocytosis. Cancer 2002;94:3023-3031.
-
(2002)
Cancer
, vol.94
, pp. 3023-3031
-
-
Imashuku, S.1
Hyakuna, N.2
Funabiki, T.3
-
9
-
-
0026065540
-
Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society
-
Henter JI, Elinder G, Ost A. Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society. Semin Oncol 1991;18:29-33.
-
(1991)
Semin Oncol
, vol.18
, pp. 29-33
-
-
Henter, J.I.1
Elinder, G.2
Ost, A.3
-
10
-
-
0030937079
-
HLH-94: A treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society
-
Henter JI, Arico M, Egeler RM, et al. HLH-94: A treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society. Med Pediatr Oncol 1997;28:342-347.
-
(1997)
Med Pediatr Oncol
, vol.28
, pp. 342-347
-
-
Henter, J.I.1
Arico, M.2
Egeler, R.M.3
-
11
-
-
0034283277
-
Cytomegalovirus DNA detection in Guthrie cards: A powerful tool for diagnosing congenital infection
-
Barbi M, Binda S, Primache V, et al. Cytomegalovirus DNA detection in Guthrie cards: A powerful tool for diagnosing congenital infection. J Clin Virol 2000;17:159-165.
-
(2000)
J Clin Virol
, vol.17
, pp. 159-165
-
-
Barbi, M.1
Binda, S.2
Primache, V.3
-
12
-
-
0038692336
-
Characteristic perforin gene mutations of haemophagocytic lymphohistiocytosis patients in Japan
-
Ueda I, Morimoto A, Inaba T, et al. Characteristic perforin gene mutations of haemophagocytic lymphohistiocytosis patients in Japan. Br J Haematol 2003;121:503-510.
-
(2003)
Br J Haematol
, vol.121
, pp. 503-510
-
-
Ueda, I.1
Morimoto, A.2
Inaba, T.3
-
13
-
-
13844250411
-
Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside
-
Matsunaga T, Kumanomido H, Shiroma M, et al. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside. Ann Otol Rhinol Laryngol 2005;114:153-160.
-
(2005)
Ann Otol Rhinol Laryngol
, vol.114
, pp. 153-160
-
-
Matsunaga, T.1
Kumanomido, H.2
Shiroma, M.3
-
14
-
-
21344464674
-
Cochlear implantation for treatment-induced ototoxic deafness in Langerhans cell histiocytosis. A case report
-
Torkos A, Czigner J, Kiss JG, et al. Cochlear implantation for treatment-induced ototoxic deafness in Langerhans cell histiocytosis. A case report. Eur Arch Otorhinolaryngol 2005;262:496-500.
-
(2005)
Eur Arch Otorhinolaryngol
, vol.262
, pp. 496-500
-
-
Torkos, A.1
Czigner, J.2
Kiss, J.G.3
-
15
-
-
3242785708
-
Rosai-Dorfman disease associated with neurosensorial hearing loss in two siblings
-
Yetiser S, Cekin E, Tosun F, Yildirim A. Rosai-Dorfman disease associated with neurosensorial hearing loss in two siblings. Int J Pediatr Otorhinolaryngol 2004;68:1095-1100.
-
(2004)
Int J Pediatr Otorhinolaryngol
, vol.68
, pp. 1095-1100
-
-
Yetiser, S.1
Cekin, E.2
Tosun, F.3
Yildirim, A.4
-
16
-
-
0037233959
-
A wider role for congenital cytomegalovirus infection in sensorineural hearingloss
-
Barbi M, Binda S, Caroppo S, et al. A wider role for congenital cytomegalovirus infection in sensorineural hearingloss. Pediatr Infect Dis J 2003;22:39-42.
-
(2003)
Pediatr Infect Dis J
, vol.22
, pp. 39-42
-
-
Barbi, M.1
Binda, S.2
Caroppo, S.3
-
17
-
-
0036808364
-
Abnormal white matter lesions with sensorineural hearing loss caused by congenital cytomegalovirus infection: Retrospective diagnosis by PCR using Guthrie cards
-
Haginoya K, Ohura T, Kon K, et al. Abnormal white matter lesions with sensorineural hearing loss caused by congenital cytomegalovirus infection: Retrospective diagnosis by PCR using Guthrie cards. Brain Dev 2002;24:710-714.
-
(2002)
Brain Dev
, vol.24
, pp. 710-714
-
-
Haginoya, K.1
Ohura, T.2
Kon, K.3
-
18
-
-
3042822500
-
Progressive bilateral sensorineural hearing loss probably induced by chronic cyclosporin A treatment after renal transplantation for focal glomerulosclerosis
-
Marioni G, Perin N, Tregnaghi A, et al. Progressive bilateral sensorineural hearing loss probably induced by chronic cyclosporin A treatment after renal transplantation for focal glomerulosclerosis. Acta Otolaryngol 2004;124:603-607.
-
(2004)
Acta Otolaryngol
, vol.124
, pp. 603-607
-
-
Marioni, G.1
Perin, N.2
Tregnaghi, A.3
-
19
-
-
0032850402
-
Sudden hearing loss associated with tacrolimus in a kidney-pancreas allograft recipient
-
Min DI, Ku YM, Rayhill S, et al. Sudden hearing loss associated with tacrolimus in a kidney-pancreas allograft recipient. Pharmacotherapy 1999;19:891-893.
-
(1999)
Pharmacotherapy
, vol.19
, pp. 891-893
-
-
Min, D.I.1
Ku, Y.M.2
Rayhill, S.3
-
20
-
-
0034814543
-
Sensorineural hearing loss and Kawasaki disease: A prospective study
-
Knott PD, Oeloff LA, Harris JP, et al. Sensorineural hearing loss and Kawasaki disease: A prospective study. Am J Otol 2001;22:343-348.
-
(2001)
Am J Otol
, vol.22
, pp. 343-348
-
-
Knott, P.D.1
Oeloff, L.A.2
Harris, J.P.3
-
21
-
-
0026448919
-
Audiologic profiles of children with Kawasaki disease
-
Sundal RP, Cleveland SS, Beiser AS, et al. Audiologic profiles of children with Kawasaki disease. Am J Otol 1992;13:512-515.
-
(1992)
Am J Otol
, vol.13
, pp. 512-515
-
-
Sundal, R.P.1
Cleveland, S.S.2
Beiser, A.S.3
-
22
-
-
0025031818
-
Sensorineural hearing loss associated with Kawasaki disease
-
Sundal RP, Newburger JW, McGill T, et al. Sensorineural hearing loss associated with Kawasaki disease. J Pediatr 1990;117:371-377.
-
(1990)
J Pediatr
, vol.117
, pp. 371-377
-
-
Sundal, R.P.1
Newburger, J.W.2
McGill, T.3
-
23
-
-
34948878419
-
A case of severe sensorineural hearing loss associated with Kawasaki disease
-
Matsuda F, Kinai E, Sugaya A, et al. A case of severe sensorineural hearing loss associated with Kawasaki disease. J Jpn Pediatr Soc 2005;109:834-838.
-
(2005)
J Jpn Pediatr Soc
, vol.109
, pp. 834-838
-
-
Matsuda, F.1
Kinai, E.2
Sugaya, A.3
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