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Year Number of Results
1945 2
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1949 24
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1951 59
1952 51
1953 65
1954 81
1955 70
1956 74
1957 76
1958 60
1959 65
1960 60
1961 56
1962 56
1963 99
1964 116
1965 109
1966 82
1967 83
1968 88
1969 122
1970 92
1971 88
1972 80
1973 81
1974 92
1975 93
1976 100
1977 135
1978 110
1979 110
1980 116
1981 134
1982 108
1983 139
1984 153
1985 141
1986 143
1987 131
1988 140
1989 112
1990 130
1991 140
1992 116
1993 154
1994 171
1995 140
1996 150
1997 137
1998 152
1999 151
2000 151
2001 153
2002 154
2003 173
2004 200
2005 163
2006 192
2007 196
2008 232
2009 221
2010 247
2011 247
2012 265
2013 270
2014 332
2015 330
2016 308
2017 325
2018 293
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2022 374
2023 297

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10,857 results

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Page 1
Langerhans-Cell Histiocytosis.
Allen CE, Merad M, McClain KL. Allen CE, et al. N Engl J Med. 2018 Aug 30;379(9):856-868. doi: 10.1056/NEJMra1607548. N Engl J Med. 2018. PMID: 30157397 Free PMC article. Review. No abstract available.
Langerhans cell histiocytosis in children: History, classification, pathobiology, clinical manifestations, and prognosis.
Krooks J, Minkov M, Weatherall AG. Krooks J, et al. J Am Acad Dermatol. 2018 Jun;78(6):1035-1044. doi: 10.1016/j.jaad.2017.05.059. J Am Acad Dermatol. 2018. PMID: 29754885 Review.
Langerhans cell histiocytosis (LCH) is an inflammatory neoplasia of myeloid precursor cells driven by mutations in the mitogen-activated protein kinase pathway. ...
Langerhans cell histiocytosis (LCH) is an inflammatory neoplasia of myeloid precursor cells driven by mutations in the
Pulmonary Langerhans' cell histiocytosis in adults.
Radzikowska E. Radzikowska E. Adv Respir Med. 2017;85(5):277-289. doi: 10.5603/ARM.a2017.0046. Epub 2017 Oct 30. Adv Respir Med. 2017. PMID: 29083024 Free article. Review.
Pulmonary Langerhans' cell histiocytosis (PLCH) is a rare disorder of unknown cause characterised by the infiltration of the lungs and other organs by the bone marrow derived Langerhans' cells, which carry mutations of BRAF gene and/or NRAS, KRAS and M …
Pulmonary Langerhans' cell histiocytosis (PLCH) is a rare disorder of unknown cause characterised by the infiltration o …
Congenital Langerhans cell histiocytosis.
Barrios K, Patiño O, Muñoz N, Moneriz C. Barrios K, et al. Biomedica. 2020 Sep 1;40(3):464-471. doi: 10.7705/biomedica.5150. Biomedica. 2020. PMID: 33030824 Free PMC article. Review. English, Spanish.
We report a case of Langerhans cell histiocytosis including a literature review focused on the clinical manifestations, diagnosis, and treatment. ...We report a case of Langerhans cell histiocytosis including a literature review focused o …
We report a case of Langerhans cell histiocytosis including a literature review focused on the clinical manifestations, …
Langerhans cell histiocytosis.
Margo CE, Goldman DR. Margo CE, et al. Surv Ophthalmol. 2008 Jul-Aug;53(4):332-58. doi: 10.1016/j.survophthal.2008.04.007. Surv Ophthalmol. 2008. PMID: 18572052 Review.
The clinical manifestations of Langerhans cell histiocytosis have been recognized for more than a century. ...By most accounts, Langerhans cell histiocytosis appears to be a morphologically benign proliferation of inflammatory cells that …
The clinical manifestations of Langerhans cell histiocytosis have been recognized for more than a century. ...By most a …
Langerhans cell histiocytosis.
Hoover KB, Rosenthal DI, Mankin H. Hoover KB, et al. Skeletal Radiol. 2007 Feb;36(2):95-104. doi: 10.1007/s00256-006-0193-2. Epub 2006 Oct 7. Skeletal Radiol. 2007. PMID: 17028900 Review.
Langerhans cell histiocytosis (LCH) is a complex disease entity comprised of three distinct clinical syndromes that demonstrate indistinguishable histology. These syndromes are: eosinophilic granuloma, which is predominantly osseous or pulmonary; Hand-Schulle
Langerhans cell histiocytosis (LCH) is a complex disease entity comprised of three distinct clinical syndromes that dem
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, Schäfer E, Nanduri V, Jubran R, Egeler RM, Janka G, Micic D, Rodriguez-Galindo C, Van Gool S, Visser J, Weitzman S, Donadieu J; Euro Histio Network. Haupt R, et al. Pediatr Blood Cancer. 2013 Feb;60(2):175-84. doi: 10.1002/pbc.24367. Epub 2012 Oct 25. Pediatr Blood Cancer. 2013. PMID: 23109216 Free PMC article.
These guidelines for the management of patients up to 18 years with Langerhans cell histiocytosis (LCH) have been set up by a group of experts involved in the Euro Histio Net project who participated in national or international studies and in peer reviewed p …
These guidelines for the management of patients up to 18 years with Langerhans cell histiocytosis (LCH) have been set u …
Pulmonary Langerhans-Cell Histiocytosis.
Qanneta R, Raventos-Estelle A. Qanneta R, et al. N Engl J Med. 2022 Dec 29;387(26):2449. doi: 10.1056/NEJMicm2203885. Epub 2022 Dec 24. N Engl J Med. 2022. PMID: 36573701 No abstract available.
Langerhans cell histiocytosis.
Windebank K, Nanduri V. Windebank K, et al. Arch Dis Child. 2009 Nov;94(11):904-8. doi: 10.1136/adc.2007.125872. Epub 2009 May 19. Arch Dis Child. 2009. PMID: 19457881 Review.
Langerhans cell histiocytosis is a rare disease. Depending on which organs are involved, the disease may prove rapidly fatal, develop a chronic reactivating but therapy-responsive pattern or resolve spontaneously. ...
Langerhans cell histiocytosis is a rare disease. Depending on which organs are involved, the disease may prove rapidly
Langerhans cell histiocytosis.
Herzog KM, Tubbs RR. Herzog KM, et al. Adv Anat Pathol. 1998 Nov;5(6):347-58. doi: 10.1097/00125480-199811000-00001. Adv Anat Pathol. 1998. PMID: 10095876 Review.
Langerhans cell histiocytosis (LCH) is a rare clonal disorder that consists of single or multiple mass lesions composed of cells with an abnormal Langerhans cell phenotype. ...Similarly, the pathogenesis of the disease is enigmatic, although the
Langerhans cell histiocytosis (LCH) is a rare clonal disorder that consists of single or multiple mass lesions composed
10,857 results
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