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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1925 1
1934 1
1945 3
1946 34
1947 26
1948 38
1949 27
1950 54
1951 71
1952 64
1953 84
1954 96
1955 81
1956 86
1957 89
1958 75
1959 86
1960 75
1961 76
1962 76
1963 130
1964 156
1965 148
1966 132
1967 137
1968 149
1969 182
1970 154
1971 167
1972 151
1973 139
1974 151
1975 175
1976 158
1977 207
1978 218
1979 186
1980 200
1981 235
1982 223
1983 255
1984 292
1985 282
1986 266
1987 266
1988 275
1989 276
1990 314
1991 333
1992 279
1993 331
1994 361
1995 347
1996 326
1997 342
1998 377
1999 363
2000 404
2001 390
2002 401
2003 467
2004 481
2005 473
2006 548
2007 565
2008 687
2009 652
2010 767
2011 768
2012 863
2013 866
2014 938
2015 908
2016 956
2017 960
2018 944
2019 935
2020 494
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22,777 results
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Page 1
Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages.
Emile JF, Abla O, Fraitag S, Horne A, Haroche J, Donadieu J, Requena-Caballero L, Jordan MB, Abdel-Wahab O, Allen CE, Charlotte F, Diamond EL, Egeler RM, Fischer A, Herrera JG, Henter JI, Janku F, Merad M, Picarsic J, Rodriguez-Galindo C, Rollins BJ, Tazi A, Vassallo R, Weiss LM; Histiocyte Society. Emile JF, et al. Blood. 2016 Jun 2;127(22):2672-81. doi: 10.1182/blood-2016-01-690636. Epub 2016 Mar 10. Blood. 2016. PMID: 26966089 Free PMC article. Review.
The histiocytoses are rare disorders characterized by the accumulation of macrophage, dendritic cell, or monocyte-derived cells in various tissues and organs of children and adults. ...We propose herein a revision of the classification of histiocytoses based on hist …
The histiocytoses are rare disorders characterized by the accumulation of macrophage, dendritic cell, or monocyte-derived cells in va …
A review of histiocytic diseases of dogs and cats.
Moore PF. Moore PF. Vet Pathol. 2014 Jan;51(1):167-84. doi: 10.1177/0300985813510413. Vet Pathol. 2014. PMID: 24395976 Review.
When histiocytomas occur as multiple lesions in skin with optional metastasis to lymph nodes and internal organs, the disease resembles cutaneous Langerhans cell histiocytosis of humans. ...Canine reactive histiocytic diseases, systemic histiocytosis (SH) and cutane …
When histiocytomas occur as multiple lesions in skin with optional metastasis to lymph nodes and internal organs, the disease resembles cuta …
[Rosai-Dorfman disease: Diagnosis and therapeutic challenges].
Cohen Aubart F, Haroche J, Emile JF, Charlotte F, Barete S, Schleinitz N, Donadieu J, Amoura Z. Cohen Aubart F, et al. Rev Med Interne. 2018 Aug;39(8):635-640. doi: 10.1016/j.revmed.2018.02.011. Epub 2018 Mar 1. Rev Med Interne. 2018. PMID: 29501513 Review. French.
The revised classification of histiocytoses published in 2016 identified various forms of RDD, from familial RDD to IgG4-associated RDD. ...
The revised classification of histiocytoses published in 2016 identified various forms of RDD, from familial RDD to IgG4-associated R …
Clinical Characteristics and Treatment of Langerhans Cell Histiocytosis.
Monsereenusorn C, Rodriguez-Galindo C. Monsereenusorn C, et al. Hematol Oncol Clin North Am. 2015 Oct;29(5):853-73. doi: 10.1016/j.hoc.2015.06.005. Epub 2015 Aug 18. Hematol Oncol Clin North Am. 2015. PMID: 26461147 Review.
Langerhans cell histiocytosis (LCH) is a disease caused by clonal proliferation of CD1a+/CD207+ cells that is characterized by a spectrum of varying degrees of organ involvement and dysfunction. ...
Langerhans cell histiocytosis (LCH) is a disease caused by clonal proliferation of CD1a+/CD207+ cells that is characterized by a spec …
[Langerhans cell histiocytosis in adults].
Néel A, Artifoni M, Donadieu J, Lorillon G, Hamidou M, Tazi A. Néel A, et al. Rev Med Interne. 2015 Oct;36(10):658-67. doi: 10.1016/j.revmed.2015.04.015. Epub 2015 Jul 3. Rev Med Interne. 2015. PMID: 26150351 Review. French.
Langerhans cell histiocytosis (LCH) is a rare disease characterized by the infiltration of one or more organs by Langerhans cell-like dendritic cells, most often organized in granulomas. ...
Langerhans cell histiocytosis (LCH) is a rare disease characterized by the infiltration of one or more organs by Langerhans cell-like …
[Child Langerhans cell histiocytosis].
Donadieu J, Héritier S. Donadieu J, et al. Presse Med. 2017 Jan;46(1):85-95. doi: 10.1016/j.lpm.2016.09.013. Epub 2017 Jan 10. Presse Med. 2017. PMID: 28087208 Review. French.
DEFINITION: Langerhans cell histiocytosis (LCH) is defined by the association of a clinical and radiological involvement and a biopsy of a pathological tissue. ...
DEFINITION: Langerhans cell histiocytosis (LCH) is defined by the association of a clinical and radiological involvement and a biopsy …
[Histiocytosis in the dermatological context of the new classification].
Lang C, Maul JT, Krähenbühl L, Dimitriou F, Dummer R. Lang C, et al. Hautarzt. 2019 Sep;70(9):691-699. doi: 10.1007/s00105-019-4460-2. Hautarzt. 2019. PMID: 31414152 Review. German.
Histiocytoses comprises a heterogeneous group of inflammatory diseases for which dendritic cells and macrophages are the main cellular components. ...Until recently, the group of histiocytosis was divided into Langerhans cell histiocytosis, non-Langerhans cel
Histiocytoses comprises a heterogeneous group of inflammatory diseases for which dendritic cells and macrophages are the main cellula
The Mayo Clinic Histiocytosis Working Group Consensus Statement for the Diagnosis and Evaluation of Adult Patients With Histiocytic Neoplasms: Erdheim-Chester Disease, Langerhans Cell Histiocytosis, and Rosai-Dorfman Disease.
Goyal G, Young JR, Koster MJ, Tobin WO, Vassallo R, Ryu JH, Davidge-Pitts CJ, Hurtado MD, Ravindran A, Sartori Valinotti JC, Bennani NN, Shah MV, Rech KL, Go RS; Mayo Clinic Histiocytosis Working Group. Goyal G, et al. Mayo Clin Proc. 2019 Oct;94(10):2054-2071. doi: 10.1016/j.mayocp.2019.02.023. Epub 2019 Aug 28. Mayo Clin Proc. 2019. PMID: 31472931
Histiocytic neoplasms, a rare and heterogeneous group of disorders, primarily include Erdheim-Chester disease, Langerhans cell histiocytosis, and Rosai-Dorfman disease. ...
Histiocytic neoplasms, a rare and heterogeneous group of disorders, primarily include Erdheim-Chester disease, Langerhans cell histiocyto
Systemic Histiocytosis (Langerhans Cell Histiocytosis, Erdheim-Chester Disease, Destombes-Rosai-Dorfman Disease): from Oncogenic Mutations to Inflammatory Disorders.
Papo M, Cohen-Aubart F, Trefond L, Bauvois A, Amoura Z, Emile JF, Haroche J. Papo M, et al. Curr Oncol Rep. 2019 May 21;21(7):62. doi: 10.1007/s11912-019-0810-6. Curr Oncol Rep. 2019. PMID: 31115724 Review.
PURPOSE OF REVIEW: Provide an overview of recent progress in decoding the pathogenesis and treatment of systemic histiocytoses. ...Those revolutionary breakthroughs enhanced our understanding of the pathogenesis of histiocytosis and led to trials with targeted thera …
PURPOSE OF REVIEW: Provide an overview of recent progress in decoding the pathogenesis and treatment of systemic histiocytoses. ...Th …
Neuroimaging features of CNS histiocytosis syndromes.
Wang Y, Camelo-Piragua S, Abdullah A, Ibrahim M, Parmar HA. Wang Y, et al. Clin Imaging. 2020 Mar;60(1):131-140. doi: 10.1016/j.clinimag.2019.10.001. Epub 2019 Dec 6. Clin Imaging. 2020. PMID: 31874337 Review.
Histiocytosis syndromes (HS) are group of heterogeneous disorders characterized by abnormal accumulation and infiltration of histiocytes, cells derived from hematopoietic cells of monocyte/macrophage lineage. ...The entities discussed in this review will include: Langerhan
Histiocytosis syndromes (HS) are group of heterogeneous disorders characterized by abnormal accumulation and infiltration of histiocy
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