Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1945 2
1946 27
1947 23
1948 36
1949 24
1950 43
1951 59
1952 51
1953 65
1954 81
1955 70
1956 74
1957 76
1958 60
1959 65
1960 61
1961 56
1962 57
1963 99
1964 116
1965 114
1966 96
1967 99
1968 101
1969 137
1970 109
1971 110
1972 87
1973 92
1974 109
1975 104
1976 105
1977 141
1978 116
1979 115
1980 121
1981 137
1982 112
1983 144
1984 162
1985 148
1986 145
1987 135
1988 146
1989 120
1990 136
1991 151
1992 128
1993 161
1994 178
1995 146
1996 156
1997 141
1998 158
1999 155
2000 152
2001 155
2002 159
2003 172
2004 202
2005 163
2006 193
2007 196
2008 236
2009 224
2010 248
2011 248
2012 263
2013 271
2014 331
2015 330
2016 307
2017 320
2018 289
2019 297
2020 219
Text availability
Article attribute
Article type
Publication date

Search Results

10,154 results
Results by year
Filters applied: . Clear all
Page 1
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 character
[Pulmonary histiocytosis X].
Fesenko OV. Fesenko OV. Ter Arkh. 2007;79(3):70-6. Ter Arkh. 2007. PMID: 17526202 Review. Russian. No abstract available.
Diagnosis and management of langerhans cell histiocytosis.
DiCaprio MR, Roberts TT. DiCaprio MR, et al. J Am Acad Orthop Surg. 2014 Oct;22(10):643-52. doi: 10.5435/JAAOS-22-10-643. J Am Acad Orthop Surg. 2014. PMID: 25281259 Review.
Langerhans cell histiocytosis is a rare group of disorders without a well-understood etiology. Known formerly as histiocytosis X, the disease has a wide spectrum of clinical presentations, including eosinophilic granuloma (solitary bone lesion),
Langerhans cell histiocytosis is a rare group of disorders without a well-understood etiology. Known formerly as his
Histiocytosis X.
Nolph MB, Luikin GA. Nolph MB, et al. Otolaryngol Clin North Am. 1982 Aug;15(3):635-48. Otolaryngol Clin North Am. 1982. PMID: 6752826 Review.
Histiocytosis X may be isolated or generalized in its clinical involvement. Spontaneous resolution may occur, although progression to diffuse systemic disease has also been found. ...
Histiocytosis X may be isolated or generalized in its clinical involvement. Spontaneous resolution may occur, although progres
Histiocytosis X. Langerhans' cell histiocytosis.
Osband ME. Osband ME. Hematol Oncol Clin North Am. 1987 Dec;1(4):737-51. Hematol Oncol Clin North Am. 1987. PMID: 3323181 Review.
Identification of the Langerhans' Cell as the Consistent Pathognomonic Cell in the Lesions of Histiocytosis X. Although the Langerhans' cell was identified more than a century ago, it has only recently been recognized as the cel
Identification of the Langerhans' Cell as the Consistent Pathognomonic Cell in the Lesions of Histiocytosis X
Langerhans cell histiocytosis (histiocytosis X).
Lam KY. Lam KY. Postgrad Med J. 1997 Jul;73(861):391-4. doi: 10.1136/pgmj.73.861.391. Postgrad Med J. 1997. PMID: 9338021 Free PMC article. Review.
There has been a renewed interest in Langerhans cell histiocytosis in recent years due both to advances in basic research and to improvements in diagnostic and treatment approaches. ...
There has been a renewed interest in Langerhans cell histiocytosis in recent years due both to advances in basic resear …
Histiocytosis X of the ear and temporal bone: review of 22 cases.
McCaffrey TV, McDonald TJ. McCaffrey TV, et al. Laryngoscope. 1979 Nov;89(11):1735-42. doi: 10.1288/00005537-197911000-00004. Laryngoscope. 1979. PMID: 315504
Histiocytosis X encompasses three syndromes characterized by the idiopathic proliferation of histiocytes: eosinophilic granuloma, Hand-Schuller-Christian syndrome, and Letterer-Siwe disease. At the Mayo Clinic between 1926 and 1978, 22 patients with histiocytosis
Histiocytosis X encompasses three syndromes characterized by the idiopathic proliferation of histiocytes: eosinophilic granulo
[Histiocytosis X].
Martínez Peric R, Villas C, Barrios RH, Sierra Sesúmaga L, Beguiristain JL. Martínez Peric R, et al. Rev Med Univ Navarra. 1993 Apr-Jun;38(2):41-7. Rev Med Univ Navarra. 1993. PMID: 14735722 Review. Spanish.
We make a clinical and bibliographical review in diagnosis and treatment of Histiocytosis X, who includes three components: Eosinophylic granuloma, Hand-Schüller-Christian disease and Letterer-Siwe syndrome. ...
We make a clinical and bibliographical review in diagnosis and treatment of Histiocytosis X, who includes three components: Eo …
Histiocytosis X and pregnancy.
DiMaggio LA, Lippes HA, Lee RV. DiMaggio LA, et al. Obstet Gynecol. 1995 May;85(5 Pt 2):806-9. doi: 10.1016/0029-7844(94)00404-2. Obstet Gynecol. 1995. PMID: 7724119 Review.
BACKGROUND: Histiocytosis X, a clinically heterogeneous infiltrating disorder, is rarely associated with pregnancy. Diabetes insipidus is a common manifestation of histiocytosis X. ...CONCLUSION: Pregnancy in patients suffering from histiocytosis
BACKGROUND: Histiocytosis X, a clinically heterogeneous infiltrating disorder, is rarely associated with pregnancy. Diabetes i …
Histiocytosis X.
Schuknecht HF. Schuknecht HF. Otolaryngol Head Neck Surg (1979). 1980 Sep-Oct;88(5):544-7. doi: 10.1177/019459988008800506. Otolaryngol Head Neck Surg (1979). 1980. PMID: 6969382
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) with a short course and poor prognosis and a milder form (type 2) with a protracted course and favorable prognosis. ...
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) w
10,154 results
Jump to page
Feedback