Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1947 1
1948 2
1949 1
1950 3
1951 3
1952 2
1953 5
1954 6
1955 6
1956 3
1957 7
1958 4
1959 3
1960 6
1961 3
1962 3
1963 3
1964 7
1965 7
1966 2
1967 5
1968 5
1969 1
1970 5
1971 2
1972 4
1973 4
1974 2
1975 1
1978 2
1979 1
1980 3
1981 3
1982 3
1983 1
1985 4
1986 4
1987 2
1988 2
1989 5
1990 4
1991 2
1992 1
1993 1
1994 1
1995 1
1996 1
1997 2
1998 1
2001 1
2008 1
2009 1
2010 3
2012 2
2013 1
2014 1
2015 2
2016 2
2020 2
2021 3
2022 2
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

169 results

Results by year

Filters applied: . Clear all
Page 1
Showing results for jan letterer
Search for Jan Detterer instead (1 results)
Eosinophilic Granuloma.
Jha SK, De Jesus O. Jha SK, et al. 2023 Aug 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 32644464 Free Books & Documents.
Lichtenstein in 1953 included eosinophilic granuloma, Hand-Schuller-Christian disease, and Letterer-Siwe disease under the disorder histiocytosis X referring to the proliferation of histiocytes (Langerhans cells) due to an unknown etiology. ...Hand-Schuller-Christian Disea …
Lichtenstein in 1953 included eosinophilic granuloma, Hand-Schuller-Christian disease, and Letterer-Siwe disease under the disorder h …
Five-Year Outcomes of Transcatheter or Surgical Aortic-Valve Replacement.
Makkar RR, Thourani VH, Mack MJ, Kodali SK, Kapadia S, Webb JG, Yoon SH, Trento A, Svensson LG, Herrmann HC, Szeto WY, Miller DC, Satler L, Cohen DJ, Dewey TM, Babaliaros V, Williams MR, Kereiakes DJ, Zajarias A, Greason KL, Whisenant BK, Hodson RW, Brown DL, Fearon WF, Russo MJ, Pibarot P, Hahn RT, Jaber WA, Rogers E, Xu K, Wheeler J, Alu MC, Smith CR, Leon MB; PARTNER 2 Investigators. Makkar RR, et al. N Engl J Med. 2020 Jan 29;382(9):799-809. doi: 10.1056/NEJMoa1910555. Print 2020 Feb 27. N Engl J Med. 2020. PMID: 31995682 Clinical Trial.
[Histiocytosis].
Veyssier-Belot C, Callot V. Veyssier-Belot C, et al. Rev Med Interne. 1996;17(11):911-23. doi: 10.1016/0248-8663(96)88121-5. Rev Med Interne. 1996. PMID: 8977972 Review. French.
Regarding Langerhans cell histiocytosis (Hand-Schuller-Christian disease, Letterer-Siwe disease and eosinophilic granuloma), the diagnosis suspected on various clinical signs, is confirmed with histological examination showing infiltration with CD1 positive histiocytes dis …
Regarding Langerhans cell histiocytosis (Hand-Schuller-Christian disease, Letterer-Siwe disease and eosinophilic granuloma), the diag …
Letterer-Siwe disease in adults.
Novice FM, Collison DW, Kleinsmith DM, Osband ME, Burdakin JH, Coskey RJ. Novice FM, et al. Cancer. 1989 Jan 1;63(1):166-74. doi: 10.1002/1097-0142(19890101)63:1<166::aid-cncr2820630127>3.0.co;2-a. Cancer. 1989. PMID: 2642729 Review.
Histiocytosis X (HX) is a rare disorder of histiocytic proliferation characterized by a broad spectrum of clinicopathologic disease. An unusual case of Letterer-Siwe disease (LSD) or subacute disseminated HX in a 71-year-old woman is presented. ...
Histiocytosis X (HX) is a rare disorder of histiocytic proliferation characterized by a broad spectrum of clinicopathologic disease. An unus …
Eosinophilic granuloma of bone.
Slater JM, Swarm OJ. Slater JM, et al. Med Pediatr Oncol. 1980;8(2):151-64. doi: 10.1002/mpo.2950080208. Med Pediatr Oncol. 1980. PMID: 6999317 Review.
Multiple sites in a single case are frequent. The clinical course is generally benign, unlike Letterer-Siwe disease or Hand-Schuller-Christian disease. A remission rate of 95% was noted, with relapses usually occurring as distant disease within the first year. ...
Multiple sites in a single case are frequent. The clinical course is generally benign, unlike Letterer-Siwe disease or Hand-Schuller- …
[Letterer-Siwe disease].
Shimazaki C, Nakagawa M. Shimazaki C, et al. Ryoikibetsu Shokogun Shirizu. 1998;(22 Pt 3):380-2. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9851167 Review. Japanese. No abstract available.
Letterer-Siwe's disease.
Niordson AM, Dano P. Niordson AM, et al. Acta Derm Venereol. 1968;48(6):612-7. Acta Derm Venereol. 1968. PMID: 4185301 No abstract available.
Specific cutaneous manifestations of internal malignancy.
Kaplan RP. Kaplan RP. Adv Dermatol. 1986;1:3-42. Adv Dermatol. 1986. PMID: 3079247 Review.
There are two malignancies seen in children under 3 years of age that often times affect the skin in a characteristic fashion. Letterer-Siwe disease, which is distinguished from other histocytic disorders by its cell of origin, the Langerhans cell, clinically shows maculop …
There are two malignancies seen in children under 3 years of age that often times affect the skin in a characteristic fashion. Letterer
[Letterer-Siwe disease].
SACREZ R, FRUHLING L, HEUMANN F, KURTZEMANN G, NICOLAS S. SACREZ R, et al. Pediatrie. 1953;8(8):909-15. Pediatrie. 1953. PMID: 13133582 Undetermined Language. No abstract available.
169 results