-
1
-
-
0023158882
-
Histiocytosis syndromes in children
-
Writing Group of the Histiocyte Society. Histiocytosis syndromes in children. Lancet. 1987;1(8526):208-209.
-
(1987)
Lancet
, vol.1
, Issue.8526
, pp. 208-209
-
-
-
3
-
-
84905107360
-
Dendritic cells, monocytes and macrophages: A unified nomenclature based on ontogeny
-
Guilliams M, Ginhoux F, Jakubzick C, et al. Dendritic cells, monocytes and macrophages: a unified nomenclature based on ontogeny. Nat Rev Immunol. 2014;14(8):571-578.
-
(2014)
Nat Rev Immunol
, vol.14
, Issue.8
, pp. 571-578
-
-
Guilliams, M.1
Ginhoux, F.2
Jakubzick, C.3
-
4
-
-
84905992289
-
Association of both Langerhans cell histiocytosis and Erdheim-Chester disease linked to the BRAFV600E mutation
-
Hervier B, Haroche J, Arnaud L, et al; French Histiocytoses Study Group. Association of both Langerhans cell histiocytosis and Erdheim-Chester disease linked to the BRAFV600E mutation. Blood. 2014;124(7):1119-1126.
-
(2014)
Blood
, vol.124
, Issue.7
, pp. 1119-1126
-
-
Hervier, B.1
Haroche, J.2
Arnaud, L.3
-
5
-
-
77956904045
-
Recurrent BRAF mutations in Langerhans cell histiocytosis
-
Badalian-Very G, Vergilio JA, Degar BA, et al. Recurrent BRAF mutations in Langerhans cell histiocytosis. Blood. 2010;116(11):1919-1923.
-
(2010)
Blood
, vol.116
, Issue.11
, pp. 1919-1923
-
-
Badalian-Very, G.1
Vergilio, J.A.2
Degar, B.A.3
-
6
-
-
84866596727
-
High prevalence of BRAF V600E mutations in Erdheim-Chester disease but not in other non-Langerhans cell histiocytoses
-
Haroche J, Charlotte F, Arnaud L, et al. High prevalence of BRAF V600E mutations in Erdheim-Chester disease but not in other non-Langerhans cell histiocytoses. Blood. 2012;120(13):2700-2703.
-
(2012)
Blood
, vol.120
, Issue.13
, pp. 2700-2703
-
-
Haroche, J.1
Charlotte, F.2
Arnaud, L.3
-
7
-
-
84909643356
-
Recurrent RAS and PIK3CA mutations in Erdheim-Chester disease
-
Emile JF, Diamond EL, Hélias-Rodzewicz Z, et al. Recurrent RAS and PIK3CA mutations in Erdheim-Chester disease. Blood. 2014;124(19):3016-3019.
-
(2014)
Blood
, vol.124
, Issue.19
, pp. 3016-3019
-
-
Emile, J.F.1
Diamond, E.L.2
Hélias-Rodzewicz, Z.3
-
8
-
-
84957056573
-
Diverse and targetable kinase alterations drive histiocytic neoplasms
-
Diamond EL, Durham BH, Haroche J, et al. Diverse and targetable kinase alterations drive histiocytic neoplasms. Cancer Discov. 2016;6(2):154-165.
-
(2016)
Cancer Discov
, vol.6
, Issue.2
, pp. 154-165
-
-
Diamond, E.L.1
Durham, B.H.2
Haroche, J.3
-
9
-
-
44149126001
-
Descriptive epidemiology of childhood Langerhans cell histiocytosis in France, 2000-2004
-
Guyot-Goubin A, Donadieu J, Barkaoui M, Bellec S, Thomas C, Clavel J. Descriptive epidemiology of childhood Langerhans cell histiocytosis in France, 2000-2004. Pediatr Blood Cancer. 2008;51(1):71-75.
-
(2008)
Pediatr Blood Cancer
, vol.51
, Issue.1
, pp. 71-75
-
-
Guyot-Goubin, A.1
Donadieu, J.2
Barkaoui, M.3
Bellec, S.4
Thomas, C.5
Clavel, J.6
-
10
-
-
44149115243
-
Incidence of Langerhans cell histiocytosis in children: A population-based study
-
Stålemark H, Laurencikas E, Karis J, Gavhed D, Fadeel B, Henter JI. Incidence of Langerhans cell histiocytosis in children: a population-based study. Pediatr Blood Cancer. 2008;51(1):76-81.
-
(2008)
Pediatr Blood Cancer
, vol.51
, Issue.1
, pp. 76-81
-
-
Stålemark, H.1
Laurencikas, E.2
Karis, J.3
Gavhed, D.4
Fadeel, B.5
Henter, J.I.6
-
11
-
-
0035144090
-
Langerhans cell histiocytosis in two generations: A new family and review of the literature
-
Aricò M, Haupt R, Russotto VS, Bossi G, Scappaticci S, Danesino C. Langerhans cell histiocytosis in two generations: a new family and review of the literature. Med Pediatr Oncol. 2001;36(2):314-316.
-
(2001)
Med Pediatr Oncol
, vol.36
, Issue.2
, pp. 314-316
-
-
Aricò, M.1
Haupt, R.2
Russotto, V.S.3
Bossi, G.4
Scappaticci, S.5
Danesino, C.6
-
12
-
-
0037075269
-
Clinical outcomes of pulmonary Langerhans'-cell histiocytosis in adults
-
Vassallo R, Ryu JH, Schroeder DR, Decker PA, Limper AH. Clinical outcomes of pulmonary Langerhans'-cell histiocytosis in adults. N Engl J Med. 2002;346(7):484-490.
-
(2002)
N Engl J Med
, vol.346
, Issue.7
, pp. 484-490
-
-
Vassallo, R.1
Ryu, J.H.2
Schroeder, D.R.3
Decker, P.A.4
Limper, A.H.5
-
13
-
-
78650078511
-
Incidence and pattern of radiological central nervous system Langerhans cell histiocytosis in children: A population based study
-
Laurencikas E, Gavhed D, Stålemark H, et al. Incidence and pattern of radiological central nervous system Langerhans cell histiocytosis in children: a population based study. Pediatr Blood Cancer. 2011;56(2):250-257.
-
(2011)
Pediatr Blood Cancer
, vol.56
, Issue.2
, pp. 250-257
-
-
Laurencikas, E.1
Gavhed, D.2
Stålemark, H.3
-
14
-
-
0029068976
-
Langerhans' cell histiocytosis. Definitive diagnosis with the use of monoclonal antibody O10 on routinely paraffin-embedded samples
-
Emile JF, Wechsler J, Brousse N, et al. Langerhans' cell histiocytosis. Definitive diagnosis with the use of monoclonal antibody O10 on routinely paraffin-embedded samples. Am J Surg Pathol. 1995;19(6):636-641.
-
(1995)
Am J Surg Pathol
, vol.19
, Issue.6
, pp. 636-641
-
-
Emile, J.F.1
Wechsler, J.2
Brousse, N.3
-
15
-
-
84871126448
-
Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years
-
Haupt R, Minkov M, Astigarraga I, et al; Euro Histio Network. Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years. Pediatr Blood Cancer. 2013;60(2):175-184.
-
(2013)
Pediatr Blood Cancer
, vol.60
, Issue.2
, pp. 175-184
-
-
Haupt, R.1
Minkov, M.2
Astigarraga, I.3
-
16
-
-
84929285115
-
Evidence of BRAF V600E in indeterminate cell tumor and interdigitating dendritic cell sarcoma
-
O'Malley DP, Agrawal R, Grimm KE, et al. Evidence of BRAF V600E in indeterminate cell tumor and interdigitating dendritic cell sarcoma. Ann Diagn Pathol. 2015;19(3):113-116.
-
(2015)
Ann Diagn Pathol
, vol.19
, Issue.3
, pp. 113-116
-
-
O'Malley, D.P.1
Agrawal, R.2
Grimm, K.E.3
-
17
-
-
84949008480
-
ETV3-NCOA2 in indeterminate cell histiocytosis: Clonal translocation supports sui generis
-
Brown RA, Kwong BY, McCalmont TH, et al. ETV3-NCOA2 in indeterminate cell histiocytosis: clonal translocation supports sui generis. Blood. 2015;126(20):2344-2345.
-
(2015)
Blood
, vol.126
, Issue.20
, pp. 2344-2345
-
-
Brown, R.A.1
Kwong, B.Y.2
McCalmont, T.H.3
-
18
-
-
12544256537
-
Langerin (CD207) staining in normal pediatric tissues, reactive lymph nodes, and childhood histiocytic disorders
-
Chikwava K, Jaffe R. Langerin (CD207) staining in normal pediatric tissues, reactive lymph nodes, and childhood histiocytic disorders. Pediatr Dev Pathol. 2004;7(6):607-614.
-
(2004)
Pediatr Dev Pathol
, vol.7
, Issue.6
, pp. 607-614
-
-
Chikwava, K.1
Jaffe, R.2
-
19
-
-
84942319855
-
Nosology and Pathology of Langerhans Cell Histiocytosis
-
Picarsic J, Jaffe R. Nosology and Pathology of Langerhans Cell Histiocytosis. Hematol Oncol Clin North Am. 2015;29(5):799-823.
-
(2015)
Hematol Oncol Clin North Am
, vol.29
, Issue.5
, pp. 799-823
-
-
Picarsic, J.1
Jaffe, R.2
-
20
-
-
84899475599
-
An unusual co-occurrence of Langerhans cell histiocytosis and Rosai-Dorfman disease: Report of a case and review of the literature
-
Cohen-Barak E, Rozenman D, Schafer J, et al. An unusual co-occurrence of Langerhans cell histiocytosis and Rosai-Dorfman disease: report of a case and review of the literature. Int J Dermatol. 2014;53(5):558-563.
-
(2014)
Int J Dermatol
, vol.53
, Issue.5
, pp. 558-563
-
-
Cohen-Barak, E.1
Rozenman, D.2
Schafer, J.3
-
21
-
-
77649228219
-
Pulmonary Langerhans cell histiocytosis associated with Hodgkin's lymphoma
-
Feuillet S, Louis L, Bergeron A, et al. Pulmonary Langerhans cell histiocytosis associated with Hodgkin's lymphoma. Eur Respir Rev. 2010;19(115):86-88.
-
(2010)
Eur Respir Rev
, vol.19
, Issue.115
, pp. 86-88
-
-
Feuillet, S.1
Louis, L.2
Bergeron, A.3
-
22
-
-
0036889611
-
Identical rearrangement of immunoglobulin heavy chain gene in neoplastic Langerhans cells and B-lymphocytes: Evidence for a common precursor
-
Magni M, Di Nicola M, Carlo-Stella C, et al. Identical rearrangement of immunoglobulin heavy chain gene in neoplastic Langerhans cells and B-lymphocytes: evidence for a common precursor. Leuk Res. 2002;26(12):1131-1133.
-
(2002)
Leuk Res
, vol.26
, Issue.12
, pp. 1131-1133
-
-
Magni, M.1
Di Nicola, M.2
Carlo-Stella, C.3
-
23
-
-
9344224571
-
A new clinical score for disease activity in Langerhans cell histiocytosis
-
Donadieu J, Piguet C, Bernard F, et al. A new clinical score for disease activity in Langerhans cell histiocytosis. Pediatr Blood Cancer. 2004;43(7):770-776.
-
(2004)
Pediatr Blood Cancer
, vol.43
, Issue.7
, pp. 770-776
-
-
Donadieu, J.1
Piguet, C.2
Bernard, F.3
-
24
-
-
33749000293
-
Long term morbidity and health related quality of life after multi-system Langerhans cell histiocytosis
-
Nanduri VR, Pritchard J, Levitt G, Glaser AW. Long term morbidity and health related quality of life after multi-system Langerhans cell histiocytosis. Eur J Cancer. 2006;42(15):2563-2569.
-
(2006)
Eur J Cancer
, vol.42
, Issue.15
, pp. 2563-2569
-
-
Nanduri, V.R.1
Pritchard, J.2
Levitt, G.3
Glaser, A.W.4
-
25
-
-
23844490896
-
Long-term follow-up of Langerhans cell histiocytosis: 39 Years' experience at a single centre
-
Bernstrand C, Sandstedt B, Ahström L, Henter JI. Long-term follow-up of Langerhans cell histiocytosis: 39 years' experience at a single centre. Acta Paediatr. 2005;94(8):1073-1084.
-
(2005)
Acta Paediatr
, vol.94
, Issue.8
, pp. 1073-1084
-
-
Bernstrand, C.1
Sandstedt, B.2
Ahström, L.3
Henter, J.I.4
-
26
-
-
0026029951
-
A xanthogranulomatous histiocytosis in a child presenting with short stature
-
Globerman H, Burstein S, Girardina PJ, Winchester P, Frankel S. A xanthogranulomatous histiocytosis in a child presenting with short stature. Am J Pediatr Hematol Oncol. 1991;13(1):42-46.
-
(1991)
Am J Pediatr Hematol Oncol
, vol.13
, Issue.1
, pp. 42-46
-
-
Globerman, H.1
Burstein, S.2
Girardina, P.J.3
Winchester, P.4
Frankel, S.5
-
27
-
-
84904871709
-
Consensus guidelines for the diagnosis and clinical management of Erdheim-Chester disease
-
Diamond EL, Dagna L, Hyman DM, et al. Consensus guidelines for the diagnosis and clinical management of Erdheim-Chester disease. Blood. 2014;124(4):483-492.
-
(2014)
Blood
, vol.124
, Issue.4
, pp. 483-492
-
-
Diamond, E.L.1
Dagna, L.2
Hyman, D.M.3
-
28
-
-
9144271975
-
Cardiovascular involvement, an overlooked feature of Erdheim-Chester disease: Report of 6 new cases and a literature review
-
Haroche J, Amoura Z, Dion E, et al. Cardiovascular involvement, an overlooked feature of Erdheim-Chester disease: report of 6 new cases and a literature review. Medicine (Baltimore). 2004;83(6):371-392.
-
(2004)
Medicine (Baltimore)
, vol.83
, Issue.6
, pp. 371-392
-
-
Haroche, J.1
Amoura, Z.2
Dion, E.3
-
29
-
-
70349774433
-
18F-fluorodeoxyglucose-positron emission tomography scanning is more useful in followup than in the initial assessment of patients with Erdheim-Chester disease
-
Arnaud L, Malek Z, Archambaud F, et al. 18F-fluorodeoxyglucose-positron emission tomography scanning is more useful in followup than in the initial assessment of patients with Erdheim-Chester disease. Arthritis Rheum. 2009;60(10):3128-3138.
-
(2009)
Arthritis Rheum
, vol.60
, Issue.10
, pp. 3128-3138
-
-
Arnaud, L.1
Malek, Z.2
Archambaud, F.3
-
30
-
-
67650709449
-
Images in cardiovascular medicine. Cardiac involvement in Erdheim-Chester disease: Magnetic resonance and computed tomographic scan imaging in a monocentric series of 37 patients
-
Haroche J, Cluzel P, Toledano D, et al. Images in cardiovascular medicine. Cardiac involvement in Erdheim-Chester disease: magnetic resonance and computed tomographic scan imaging in a monocentric series of 37 patients. Circulation. 2009;119(25):e597-e598.
-
(2009)
Circulation
, vol.119
, Issue.25
, pp. e597-e598
-
-
Haroche, J.1
Cluzel, P.2
Toledano, D.3
-
31
-
-
79953124751
-
CNS involvement and treatment with interferon-α are independent prognostic factors in Erdheim-Chester disease: A multicenter survival analysis of 53 patients
-
Arnaud L, Hervier B, Néel A, et al. CNS involvement and treatment with interferon-α are independent prognostic factors in Erdheim-Chester disease: a multicenter survival analysis of 53 patients. Blood. 2011;117(10):2778-2782.
-
(2011)
Blood
, vol.117
, Issue.10
, pp. 2778-2782
-
-
Arnaud, L.1
Hervier, B.2
Néel, A.3
-
32
-
-
53449084408
-
ALK+ histiocytosis: A novel type of systemic histiocytic proliferative disorder of early infancy
-
Chan JK, Lamant L, Algar E, et al. ALK+ histiocytosis: a novel type of systemic histiocytic proliferative disorder of early infancy. Blood. 2008;112(7):2965-2968.
-
(2008)
Blood
, vol.112
, Issue.7
, pp. 2965-2968
-
-
Chan, J.K.1
Lamant, L.2
Algar, E.3
-
33
-
-
84859593606
-
B-RAF mutant alleles associated with Langerhans cell histiocytosis, a granulomatous pediatric disease
-
published correction appears in PLoS One. 2012;7(6)
-
Satoh T, Smith A, Sarde A, et al. B-RAF mutant alleles associated with Langerhans cell histiocytosis, a granulomatous pediatric disease [published correction appears in PLoS One. 2012;7(6)]. PLoS One. 2012;7(4):e33891.
-
(2012)
PLoS One
, vol.7
, Issue.4
-
-
Satoh, T.1
Smith, A.2
Sarde, A.3
-
34
-
-
84897944839
-
BRAF-V600E expression in precursor versus differentiated dendritic cells defines clinically distinct LCH risk groups
-
published correction appears in J Exp Med. 2015;212(2):281
-
Berres ML, Lim KP, Peters T, et al. BRAF-V600E expression in precursor versus differentiated dendritic cells defines clinically distinct LCH risk groups [published correction appears in J Exp Med. 2015;212(2):281]. J Exp Med. 2014;211(4):669-683.
-
(2014)
J Exp Med
, vol.211
, Issue.4
, pp. 669-683
-
-
Berres, M.L.1
Lim, K.P.2
Peters, T.3
-
35
-
-
84866624067
-
BRAFV600E mutant protein is expressed in cells of variable maturation in Langerhans cell histiocytosis
-
Sahm F, Capper D, Preusser M, et al. BRAFV600E mutant protein is expressed in cells of variable maturation in Langerhans cell histiocytosis. Blood. 2012;120(12):e28-e34.
-
(2012)
Blood
, vol.120
, Issue.12
, pp. e28-e34
-
-
Sahm, F.1
Capper, D.2
Preusser, M.3
-
36
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, et al. Mutations of the BRAF gene in human cancer. Nature. 2002;417(6892):949-954.
-
(2002)
Nature
, vol.417
, Issue.6892
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
-
37
-
-
84909609809
-
Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis
-
Chakraborty R, Hampton OA, Shen X, et al. Mutually exclusive recurrent somatic mutations in MAP2K1 and BRAF support a central role for ERK activation in LCH pathogenesis. Blood. 2014;124(19):3007-3015.
-
(2014)
Blood
, vol.124
, Issue.19
, pp. 3007-3015
-
-
Chakraborty, R.1
Hampton, O.A.2
Shen, X.3
-
38
-
-
84907009615
-
High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis
-
Brown NA, Furtado LV, Betz BL, et al. High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis. Blood. 2014;124(10):1655-1658.
-
(2014)
Blood
, vol.124
, Issue.10
, pp. 1655-1658
-
-
Brown, N.A.1
Furtado, L.V.2
Betz, B.L.3
-
39
-
-
84901424838
-
Somatic activating ARAF mutations in Langerhans cell histiocytosis
-
Nelson DS, Quispel W, Badalian-Very G, et al. Somatic activating ARAF mutations in Langerhans cell histiocytosis. Blood. 2014;123(20):3152-3155.
-
(2014)
Blood
, vol.123
, Issue.20
, pp. 3152-3155
-
-
Nelson, D.S.1
Quispel, W.2
Badalian-Very, G.3
-
41
-
-
84927673688
-
Common cancer-associated PIK3CA activating mutations rarely occur in Langerhans cell histiocytosis
-
Héritier S, Saffroy R, Radosevic-Robin N, et al. Common cancer-associated PIK3CA activating mutations rarely occur in Langerhans cell histiocytosis. Blood. 2015;125(15):2448-2449.
-
(2015)
Blood
, vol.125
, Issue.15
, pp. 2448-2449
-
-
Héritier, S.1
Saffroy, R.2
Radosevic-Robin, N.3
-
42
-
-
84886878689
-
Detectionof an NRAS mutationin Erdheim-Chester disease
-
Diamond EL, Abdel-Wahab O, Pentsova E, et al. Detectionof an NRAS mutationin Erdheim-Chester disease. Blood. 2013;122(6):1089-1091.
-
(2013)
Blood
, vol.122
, Issue.6
, pp. 1089-1091
-
-
Diamond, E.L.1
Abdel-Wahab, O.2
Pentsova, E.3
-
43
-
-
84904320952
-
Frequent detection of BRAF(V600E) mutations in histiocytic and dendritic cell neoplasms
-
Go H, Jeon YK, Huh J, et al. Frequent detection of BRAF(V600E) mutations in histiocytic and dendritic cell neoplasms. Histopathology. 2014;65(2):261-272.
-
(2014)
Histopathology
, vol.65
, Issue.2
, pp. 261-272
-
-
Go, H.1
Jeon, Y.K.2
Huh, J.3
-
44
-
-
84918571169
-
BRAF(V600E) mutation in a histiocytic sarcoma arising from hairy cell leukemia
-
Michonneau D, Kaltenbach S, Derrieux C, et al. BRAF(V600E) mutation in a histiocytic sarcoma arising from hairy cell leukemia. J Clin Oncol. 2014;32(35):e117-e121.
-
(2014)
J Clin Oncol
, vol.32
, Issue.35
, pp. e117-e121
-
-
Michonneau, D.1
Kaltenbach, S.2
Derrieux, C.3
-
45
-
-
84925547021
-
Dramatic response of a BRAF V600E-mutated primary CNS histiocytic sarcoma to vemurafenib
-
Idbaih A, Mokhtari K, Emile JF, et al. Dramatic response of a BRAF V600E-mutated primary CNS histiocytic sarcoma to vemurafenib. Neurology. 2014;83(16):1478-1480.
-
(2014)
Neurology
, vol.83
, Issue.16
, pp. 1478-1480
-
-
Idbaih, A.1
Mokhtari, K.2
Emile, J.F.3
-
46
-
-
84908127440
-
The BRAF-V600E mutation in circulating cell-free DNA is a promising biomarker of high-risk adult Langerhans cell histiocytosis
-
Kobayashi M, Tojo A. The BRAF-V600E mutation in circulating cell-free DNA is a promising biomarker of high-risk adult Langerhans cell histiocytosis. Blood. 2014;124(16):2610-2611.
-
(2014)
Blood
, vol.124
, Issue.16
, pp. 2610-2611
-
-
Kobayashi, M.1
Tojo, A.2
-
47
-
-
84922372527
-
Prospective blinded study of BRAFV600E mutation detection in cell-free DNA of patients with systemic histiocytic disorders
-
Hyman DM, Diamond EL, Vibat CR, et al. Prospective blinded study of BRAFV600E mutation detection in cell-free DNA of patients with systemic histiocytic disorders. Cancer Discov. 2015;5(1):64-71.
-
(2015)
Cancer Discov
, vol.5
, Issue.1
, pp. 64-71
-
-
Hyman, D.M.1
Diamond, E.L.2
Vibat, C.R.3
-
48
-
-
84876498502
-
Dramatic efficacy of vemurafenib in both multisystemic and refractory Erdheim-Chester disease and Langerhans cell histiocytosis harboring the BRAF V600E mutation
-
Haroche J, Cohen-Aubart F, Emile JF, et al. Dramatic efficacy of vemurafenib in both multisystemic and refractory Erdheim-Chester disease and Langerhans cell histiocytosis harboring the BRAF V600E mutation. Blood. 2013;121(9):1495-1500.
-
(2013)
Blood
, vol.121
, Issue.9
, pp. 1495-1500
-
-
Haroche, J.1
Cohen-Aubart, F.2
Emile, J.F.3
-
49
-
-
84922354803
-
Reproducible and sustained efficacy of targeted therapy with vemurafenib in patients with BRAF (V600E)-mutated Erdheim-Chester disease
-
Haroche J, Cohen-Aubart F, Emile JF, et al. Reproducible and sustained efficacy of targeted therapy with vemurafenib in patients with BRAF (V600E)-mutated Erdheim-Chester disease. J Clin Oncol. 2015;33(5):411-418.
-
(2015)
J Clin Oncol
, vol.33
, Issue.5
, pp. 411-418
-
-
Haroche, J.1
Cohen-Aubart, F.2
Emile, J.F.3
-
50
-
-
84939864059
-
Vemurafenib in multiple nonmelanoma cancers with BRAF V600 mutations
-
Hyman DM, Puzanov I, Subbiah V, et al. Vemurafenib in multiple nonmelanoma cancers with BRAF V600 mutations. N Engl J Med. 2015;373(8):726-736.
-
(2015)
N Engl J Med
, vol.373
, Issue.8
, pp. 726-736
-
-
Hyman, D.M.1
Puzanov, I.2
Subbiah, V.3
-
51
-
-
84965093707
-
Vemurafenib use in an infant for high-risk Langerhans cell histiocytosis
-
Héritier S, Jehanne M, Leverger G, et al. Vemurafenib use in an infant for high-risk Langerhans cell histiocytosis. JAMA Oncol. 2015;1(6):836-838.
-
(2015)
JAMA Oncol
, vol.1
, Issue.6
, pp. 836-838
-
-
Héritier, S.1
Jehanne, M.2
Leverger, G.3
-
52
-
-
0034787191
-
Xanthogranuloma is the archetype of non-Langerhans cell histiocytoses
-
Zelger BWH, Cerio R. Xanthogranuloma is the archetype of non-Langerhans cell histiocytoses. Br J Dermatol. 2001;145(2):369-371.
-
(2001)
Br J Dermatol
, vol.145
, Issue.2
, pp. 369-371
-
-
Zelger, B.W.H.1
Cerio, R.2
-
53
-
-
0035230295
-
The cutaneous "histiocytoses"
-
Zelger B, Burgdorf WH. The cutaneous "histiocytoses". Adv Dermatol. 2001;17:77-114.
-
(2001)
Adv Dermatol
, vol.17
, pp. 77-114
-
-
Zelger, B.1
Burgdorf, W.H.2
-
54
-
-
23044474059
-
Uncommon histiocytic disorders: The non-Langerhans cell histiocytoses
-
Weitzman S, Jaffe R. Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses. Pediatr Blood Cancer. 2005;45(3):256-264.
-
(2005)
Pediatr Blood Cancer
, vol.45
, Issue.3
, pp. 256-264
-
-
Weitzman, S.1
Jaffe, R.2
-
55
-
-
84879767263
-
A histiocytic disorder that does not easily fit into the classification of the juvenile xanthogranuloma family
-
Stinco G, Patriarca M, Di Loreto C, Patrone P. A histiocytic disorder that does not easily fit into the classification of the juvenile xanthogranuloma family. Int J Dermatol. 2013;52(7):849-855.
-
(2013)
Int J Dermatol
, vol.52
, Issue.7
, pp. 849-855
-
-
Stinco, G.1
Patriarca, M.2
Di Loreto, C.3
Patrone, P.4
-
57
-
-
0037407915
-
Juvenile xanthogranulomas in the first two decades of life: A clinicopathologic study of 174 cases with cutaneous and extracutaneous manifestations
-
Dehner LP. Juvenile xanthogranulomas in the first two decades of life: a clinicopathologic study of 174 cases with cutaneous and extracutaneous manifestations. Am J Surg Pathol. 2003;27(5):579-593.
-
(2003)
Am J Surg Pathol
, vol.27
, Issue.5
, pp. 579-593
-
-
Dehner, L.P.1
-
58
-
-
84858794216
-
Generalized eruptive histiocytomas and juvenile eruptive xanthogranulomas in a 10-year-old boy: A potpourri of exotic terms indicating the need for unification
-
Verma SB. Generalized eruptive histiocytomas and juvenile eruptive xanthogranulomas in a 10-year-old boy: a potpourri of exotic terms indicating the need for unification. Int J Dermatol. 2012;51(4):445-447.
-
(2012)
Int J Dermatol
, vol.51
, Issue.4
, pp. 445-447
-
-
Verma, S.B.1
-
59
-
-
84867380970
-
Multicentric reticulohistiocytosis and fibroblastic rheumatism
-
Trotta F, Colina M. Multicentric reticulohistiocytosis and fibroblastic rheumatism. Best Pract Res Clin Rheumatol. 2012;26(4):543-557.
-
(2012)
Best Pract Res Clin Rheumatol
, vol.26
, Issue.4
, pp. 543-557
-
-
Trotta, F.1
Colina, M.2
-
60
-
-
0035985576
-
Tumours of histiocytes and accessory dendritic cells: An immunohistochemical approach to classification from the International Lymphoma Study Group based on 61 cases
-
Pileri SA, Grogan TM, Harris NL, et al. Tumours of histiocytes and accessory dendritic cells: an immunohistochemical approach to classification from the International Lymphoma Study Group based on 61 cases. Histopathology. 2002;41(1):1-29.
-
(2002)
Histopathology
, vol.41
, Issue.1
, pp. 1-29
-
-
Pileri, S.A.1
Grogan, T.M.2
Harris, N.L.3
-
61
-
-
84891777842
-
A case of interdigitating dendritic cell sarcoma/histiocytic sarcoma-a diagnostic pitfall
-
Johnson RL, Boisot S, Ball ED, Wang HY. A case of interdigitating dendritic cell sarcoma/histiocytic sarcoma-a diagnostic pitfall. Int J Clin Exp Pathol. 2014;7(1):378-385.
-
(2014)
Int J Clin Exp Pathol
, vol.7
, Issue.1
, pp. 378-385
-
-
Johnson, R.L.1
Boisot, S.2
Ball, E.D.3
Wang, H.Y.4
-
62
-
-
84890013122
-
The genetics of interdigitating dendritic cell sarcoma share some changes with Langerhans cell histiocytosis in select cases
-
O'Malley DP, Zuckerberg L, Smith LB, et al. The genetics of interdigitating dendritic cell sarcoma share some changes with Langerhans cell histiocytosis in select cases. Ann Diagn Pathol. 2014;18(1):18-20.
-
(2014)
Ann Diagn Pathol
, vol.18
, Issue.1
, pp. 18-20
-
-
O'Malley, D.P.1
Zuckerberg, L.2
Smith, L.B.3
-
63
-
-
47049116151
-
Clonally related follicular lymphomas and histiocytic/dendritic cell sarcomas: Evidence for transdifferentiation of the follicular lymphoma clone
-
Feldman AL, Arber DA, Pittaluga S, et al. Clonally related follicular lymphomas and histiocytic/dendritic cell sarcomas: evidence for transdifferentiation of the follicular lymphoma clone. Blood. 2008;111(12):5433-5439.
-
(2008)
Blood
, vol.111
, Issue.12
, pp. 5433-5439
-
-
Feldman, A.L.1
Arber, D.A.2
Pittaluga, S.3
-
64
-
-
80455155161
-
Clonally related histiocytic/dendritic cell sarcoma and chronic lymphocytic leukemia/small lymphocytic lymphoma: A study of seven cases
-
Shao H, Xi L, Raffeld M, et al. Clonally related histiocytic/dendritic cell sarcoma and chronic lymphocytic leukemia/small lymphocytic lymphoma: a study of seven cases. Mod Pathol. 2011;24(11):1421-1432.
-
(2011)
Mod Pathol
, vol.24
, Issue.11
, pp. 1421-1432
-
-
Shao, H.1
Xi, L.2
Raffeld, M.3
-
65
-
-
84879520389
-
Langerhans cell sarcoma arising from chronic lymphocytic lymphoma/small lymphocytic leukemia: Lineage analysis and BRAF V600E mutation study
-
Chen W, Jaffe R, Zhang L, et al. Langerhans cell sarcoma arising from chronic lymphocytic lymphoma/small lymphocytic leukemia: lineage analysis and BRAF V600E mutation study. N Am J Med Sci. 2013;5(6):386-391.
-
(2013)
N Am J Med Sci
, vol.5
, Issue.6
, pp. 386-391
-
-
Chen, W.1
Jaffe, R.2
Zhang, L.3
-
66
-
-
77956214943
-
Clinicopathologic features of histiocytic lesions following ALL, with a review of the literature
-
Castro EC, Blazquez C, Boyd J, et al. Clinicopathologic features of histiocytic lesions following ALL, with a review of the literature. Pediatr Dev Pathol. 2010;13(3):225-237.
-
(2010)
Pediatr Dev Pathol
, vol.13
, Issue.3
, pp. 225-237
-
-
Castro, E.C.1
Blazquez, C.2
Boyd, J.3
-
67
-
-
77955171367
-
Histiocytic sarcoma and underlying chronic myelomonocytic leukemia: A proposal for the developmental classification of histiocytic sarcoma
-
Mori M, Matsushita A, Takiuchi Y, et al. Histiocytic sarcoma and underlying chronic myelomonocytic leukemia: a proposal for the developmental classification of histiocytic sarcoma. Int J Hematol. 2010;92(1):168-173.
-
(2010)
Int J Hematol
, vol.92
, Issue.1
, pp. 168-173
-
-
Mori, M.1
Matsushita, A.2
Takiuchi, Y.3
-
68
-
-
84870171240
-
Langerhans cell histiocytosis first presenting in the skin in adults: Frequent association with a second haematological malignancy
-
Edelbroek JR, Vermeer MH, Jansen PM, et al. Langerhans cell histiocytosis first presenting in the skin in adults: frequent association with a second haematological malignancy. Br J Dermatol. 2012;167(6):1287-1294.
-
(2012)
Br J Dermatol
, vol.167
, Issue.6
, pp. 1287-1294
-
-
Edelbroek, J.R.1
Vermeer, M.H.2
Jansen, P.M.3
-
69
-
-
0014447292
-
Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity
-
Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity. Arch Pathol. 1969;87(1):63-70.
-
(1969)
Arch Pathol
, vol.87
, Issue.1
, pp. 63-70
-
-
Rosai, J.1
Dorfman, R.F.2
-
70
-
-
0015332112
-
Pseudotumoral lymph node lipidic histiocytosis. Further case in a young Martinique woman
-
in French
-
Destombes P, Destombes M, Martin L. Pseudotumoral lymph node lipidic histiocytosis. Further case in a young Martinique woman [in French]. Bull Soc Pathol Exot. 1972;65(3):481-488.
-
(1972)
Bull Soc Pathol Exot
, vol.65
, Issue.3
, pp. 481-488
-
-
Destombes, P.1
Destombes, M.2
Martin, L.3
-
71
-
-
84899690339
-
Updates on histiocytic disorders
-
Vaiselbuh SR, Bryceson YT, Allen CE, Whitlock JA, Abla O. Updates on histiocytic disorders. Pediatr Blood Cancer. 2014;61(7):1329-1335.
-
(2014)
Pediatr Blood Cancer
, vol.61
, Issue.7
, pp. 1329-1335
-
-
Vaiselbuh, S.R.1
Bryceson, Y.T.2
Allen, C.E.3
Whitlock, J.A.4
Abla, O.5
-
72
-
-
84947648684
-
Primary Rosai-Dorfman disease of bone: A clinicopathologic study of 15 cases
-
Demicco EG, Rosenberg AE, Björnsson J, Rybak LD, Unni KK, Nielsen GP. Primary Rosai-Dorfman disease of bone: a clinicopathologic study of 15 cases. Am J Surg Pathol. 2010;34(9):1324-1333.
-
(2010)
Am J Surg Pathol
, vol.34
, Issue.9
, pp. 1324-1333
-
-
Demicco, E.G.1
Rosenberg, A.E.2
Björnsson, J.3
Rybak, L.D.4
Unni, K.K.5
Nielsen, G.P.6
-
73
-
-
0035082477
-
Rosai-Dorfman disease isolated to the central nervous system: A report of 11 cases
-
Andriko JA, Morrison A, Colegial CH, Davis BJ, Jones RV. Rosai-Dorfman disease isolated to the central nervous system: a report of 11 cases. Mod Pathol. 2001;14(3):172-178.
-
(2001)
Mod Pathol
, vol.14
, Issue.3
, pp. 172-178
-
-
Andriko, J.A.1
Morrison, A.2
Colegial, C.H.3
Davis, B.J.4
Jones, R.V.5
-
74
-
-
84951174873
-
A case report of meningeal Rosai-Dorfman disease associated with IgG4-related disease
-
Tauziede-Espariat A, Polivka M, Chabriat H, Bouazza S, Sene D, Adle-Biassette H. A case report of meningeal Rosai-Dorfman disease associated with IgG4-related disease. Clin Neuropathol. 2015;34(6):343-349.
-
(2015)
Clin Neuropathol
, vol.34
, Issue.6
, pp. 343-349
-
-
Tauziede-Espariat, A.1
Polivka, M.2
Chabriat, H.3
Bouazza, S.4
Sene, D.5
Adle-Biassette, H.6
-
75
-
-
84873741930
-
Cutaneous revelation of Rosai-Dorfman disease: 7 Cases
-
in French
-
Vuong V, Moulonguet I, Cordoliani F, et al. Cutaneous revelation of Rosai-Dorfman disease: 7 cases [in French]. Ann Dermatol Venereol. 2013;140(2):83-90.
-
(2013)
Ann Dermatol Venereol
, vol.140
, Issue.2
, pp. 83-90
-
-
Vuong, V.1
Moulonguet, I.2
Cordoliani, F.3
-
76
-
-
84892439034
-
A subset of Rosai-Dorfman disease cases show increased IgG4-positive plasma cells: Another red herring or a true association with IgG4-related disease?
-
Menon MP, Evbuomwan MO, Rosai J, Jaffe ES, Pittaluga S. A subset of Rosai-Dorfman disease cases show increased IgG4-positive plasma cells: another red herring or a true association with IgG4-related disease? Histopathology. 2014;64(3):455-459.
-
(2014)
Histopathology
, vol.64
, Issue.3
, pp. 455-459
-
-
Menon, M.P.1
Evbuomwan, M.O.2
Rosai, J.3
Jaffe, E.S.4
Pittaluga, S.5
-
77
-
-
0034794078
-
Rosai-Dorfman disease complicated by autoimmune haemolytic anaemia: Case report and review of a multisystem disease with cutaneous infiltrates
-
Grabczynska SA, Toh CT, Francis N, Costello C, Bunker CB. Rosai-Dorfman disease complicated by autoimmune haemolytic anaemia: case report and review of a multisystem disease with cutaneous infiltrates. Br J Dermatol. 2001;145(2):323-326.
-
(2001)
Br J Dermatol
, vol.145
, Issue.2
, pp. 323-326
-
-
Grabczynska, S.A.1
Toh, C.T.2
Francis, N.3
Costello, C.4
Bunker, C.B.5
-
79
-
-
84855445021
-
A mild form of SLC29A3 disorder: A frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant
-
Bolze A, Abhyankar A, Grant AV, et al. A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant. PLoS One. 2012;7(1):e29708.
-
(2012)
PLoS One
, vol.7
, Issue.1
-
-
Bolze, A.1
Abhyankar, A.2
Grant, A.V.3
-
80
-
-
21244462801
-
Histologic features of sinus histiocytosis with massive lymphadenopathy in patients with autoimmune lymphoproliferative syndrome
-
Maric I, Pittaluga S, Dale JK, et al. Histologic features of sinus histiocytosis with massive lymphadenopathy in patients with autoimmune lymphoproliferative syndrome. Am J Surg Pathol. 2005;29(7):903-911.
-
(2005)
Am J Surg Pathol
, vol.29
, Issue.7
, pp. 903-911
-
-
Maric, I.1
Pittaluga, S.2
Dale, J.K.3
-
81
-
-
84855932987
-
Familial and acquired hemophagocytic lymphohistiocytosis
-
Janka GE. Familial and acquired hemophagocytic lymphohistiocytosis. Annu Rev Med. 2012;63:233-246.
-
(2012)
Annu Rev Med
, vol.63
, pp. 233-246
-
-
Janka, G.E.1
-
82
-
-
0025787766
-
Hypercytokinemia in familial hemophagocytic lymphohistiocytosis
-
Henter JI, Elinder G, Söder O, Hansson M, Andersson B, Andersson U. Hypercytokinemia in familial hemophagocytic lymphohistiocytosis. Blood. 1991;78(11):2918-2922.
-
(1991)
Blood
, vol.78
, Issue.11
, pp. 2918-2922
-
-
Henter, J.I.1
Elinder, G.2
Söder, O.3
Hansson, M.4
Andersson, B.5
Andersson, U.6
-
83
-
-
33845619137
-
HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
-
Henter JI, Horne A, Aricó M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer. 2007;48(2):124-131.
-
(2007)
Pediatr Blood Cancer
, vol.48
, Issue.2
, pp. 124-131
-
-
Henter, J.I.1
Horne, A.2
Aricó, M.3
-
84
-
-
0022650751
-
Allogeneic bone marrow transplantation for erythrophagocytic lymphohistiocytosis
-
Fischer A, Cerf-Bensussan N, Blanche S, et al. Allogeneic bone marrow transplantation for erythrophagocytic lymphohistiocytosis. J Pediatr. 1986;108(2):267-270.
-
(1986)
J Pediatr
, vol.108
, Issue.2
, pp. 267-270
-
-
Fischer, A.1
Cerf-Bensussan, N.2
Blanche, S.3
-
85
-
-
80055079785
-
Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: Long-term results of the HLH-94 treatment protocol
-
Trottestam H, Horne A, Aricò M, et al; Histiocyte Society. Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol. Blood. 2011;118(17):4577-4584.
-
(2011)
Blood
, vol.118
, Issue.17
, pp. 4577-4584
-
-
Trottestam, H.1
Horne, A.2
Aricò, M.3
-
86
-
-
77951676108
-
Inherited defects in lymphocyte cytotoxic activity
-
published correction appears in Immunol Rev. 2010;236(1):276
-
Pachlopnik Schmid J, Côte M, Ménager MM, et al. Inherited defects in lymphocyte cytotoxic activity [published correction appears in Immunol Rev. 2010;236(1):276]. Immunol Rev. 2010;235(1):10-23.
-
(2010)
Immunol Rev
, vol.235
, Issue.1
, pp. 10-23
-
-
Pachlopnik Schmid, J.1
Côte, M.2
Ménager, M.M.3
-
87
-
-
84927126118
-
An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome
-
Canna SW, de Jesus AA, Gouni S, et al. An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome. Nat Genet. 2014;46(10):1140-1146.
-
(2014)
Nat Genet
, vol.46
, Issue.10
, pp. 1140-1146
-
-
Canna, S.W.1
De Jesus, A.A.2
Gouni, S.3
-
88
-
-
84922008927
-
Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation
-
Romberg N, Al Moussawi K, Nelson-Williams C, et al. Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation. Nat Genet. 2014;46(10):1135-1139.
-
(2014)
Nat Genet
, vol.46
, Issue.10
, pp. 1135-1139
-
-
Romberg, N.1
Al Moussawi, K.2
Nelson-Williams, C.3
-
89
-
-
84953635379
-
Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry
-
Cetica V, Sieni E, Pende D, et al. Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry. J Allergy Clin Immunol. 2016;137(1):188-196.e4.
-
(2016)
J Allergy Clin Immunol
, vol.137
, Issue.1
, pp. 188.e4-196.e4
-
-
Cetica, V.1
Sieni, E.2
Pende, D.3
-
90
-
-
82155184541
-
Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH
-
Zhang K, Jordan MB, Marsh RA, et al. Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH. Blood. 2011;118(22):5794-5798.
-
(2011)
Blood
, vol.118
, Issue.22
, pp. 5794-5798
-
-
Zhang, K.1
Jordan, M.B.2
Marsh, R.A.3
-
91
-
-
84936095269
-
The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: Implications for differential diagnosis and pathogenesis
-
Bode SF, Ammann S, Al-Herz W, et al; Inborn Errors Working Party of the EBMT. The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis. Haematologica. 2015;100(7):978-988.
-
(2015)
Haematologica
, vol.100
, Issue.7
, pp. 978-988
-
-
Bode, S.F.1
Ammann, S.2
Al-Herz, W.3
-
92
-
-
84899658785
-
Adult haemophagocytic syndrome
-
Ramos-Casals M, Brito-Zerón P, López-Guillermo A, Khamashta MA, Bosch X. Adult haemophagocytic syndrome. Lancet. 2014;383(9927):1503-1516.
-
(2014)
Lancet
, vol.383
, Issue.9927
, pp. 1503-1516
-
-
Ramos-Casals, M.1
Brito-Zerón, P.2
López-Guillermo, A.3
Khamashta, M.A.4
Bosch, X.5
-
93
-
-
78650764207
-
Treatment of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis (EBV-HLH); update 2010
-
Imashuku S. Treatment of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis (EBV-HLH); update 2010. J Pediatr Hematol Oncol. 2011;33(1):35-39.
-
(2011)
J Pediatr Hematol Oncol
, vol.33
, Issue.1
, pp. 35-39
-
-
Imashuku, S.1
-
94
-
-
0035990141
-
Is macrophage activation syndrome a new entity?
-
Athreya BH. Is macrophage activation syndrome a new entity? Clin Exp Rheumatol. 2002;20(2):121-123.
-
(2002)
Clin Exp Rheumatol
, vol.20
, Issue.2
, pp. 121-123
-
-
Athreya, B.H.1
-
95
-
-
0036247156
-
Macrophage activation syndrome is hemophagocytic lymphohistiocytosis-need for the right terminology
-
Ramanan AV, Baildam EM. Macrophage activation syndrome is hemophagocytic lymphohistiocytosis-need for the right terminology. J Rheumatol. 2002;29(5):1105.
-
(2002)
J Rheumatol
, vol.29
, Issue.5
, pp. 1105
-
-
Ramanan, A.V.1
Baildam, E.M.2
|