Zobrazeno 1 - 10
of 5 273
pro vyhledávání: '"letterer-siwe disease"'
Autor:
H. H., Suad1 Dr.suadhassan4@gmail.com, Elamin, Mona Mohamed2, Modawe, Gad Allah3, Awad Elseed, Khalid Abd Elmohsin4
Publikováno v:
Sudan Journal of Medical Sciences. Sep2018, Vol. 13 Issue 3, p207-218. 12p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Sudan Journal of Medical Sciences, Vol 13, Pp 1-12 (2018)
Background: Letterer–Siwe Disease (LSD) is one of the variants of Langerhans cell histiocytosis (LCH), which is considered as a rare disease that affects many systems in the body; it is characterized by monoclonal migration and proliferation of spe
Externí odkaz:
https://doaj.org/article/31e1277986ca403c96fdcbb594888eee
Autor:
Doya, Leen Jamel1 (AUTHOR) dr.leen.doya@gmail.com, Dib, Ghazal1 (AUTHOR), Hassan, Fouz2 (AUTHOR)
Publikováno v:
Oxford Medical Case Reports. Jul2021, Vol. 2021 Issue 7, p1-3. 3p.
Publikováno v:
Indian Journal of Pathology and Oncology. 8:508-511
Background: Histiocytes with coffee bean like nucleus are the diagnostic hallmark of Langerhans cell histiocytosis (LCH) supported with immunohistochemical (IHC) demonstration of fascin, CD1a and S-100. We report a case of Letterer-Siwe disease in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62e4d309268028e862245e1e1139d025
https://doi.org/10.18231/j.ijpo.2021.105
https://doi.org/10.18231/j.ijpo.2021.105
Publikováno v:
Oxford Medical Case Reports
Langerhans cell histiocytosis (LCH) is a rare disease of unknown etiology that affects several organs. The fatal type of Langerhans cell histiocytosis is called Letterer Siwe disease (LSD) which is multisystem with a poor prognosis. Herein, we report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c367100626c634468a78304e8df8ce0
https://doi.org/10.1093/omcr/omab058
https://doi.org/10.1093/omcr/omab058
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Srivastava, Nimisha, Gupta, Rishabh
Publikováno v:
In Drug Delivery Systems for Metabolic Disorders 2022:149-160
Publikováno v:
Indian Journal of Drugs in Dermatology, Vol 6, Iss 2, Pp 91-93 (2020)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e62707b687ab044a0580cec4643e1390
http://www.ijdd.in/article.asp?issn=2455-3972
http://www.ijdd.in/article.asp?issn=2455-3972
Autor:
Olga V. Domanskaya, Olga A. Zagorodnikova, Nataliya V. Selivanova, Sergey A. Dudkin, Olga I. Andriyanova, Nataliya V. Matveeva, Farok K. Manerov, Yakov Y. Yakovlev
Abt-Letterer-Siwe disease is a form of Langerhans cell histiocytosis and occurs in 2–10 cases per 1 million of the child population per year. The Russian and foreign literature provide descriptions of this disease in children of different ages. Fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9af3e73d7d916632ab37f4bede2b191f
http://www.intechopen.com/articles/show/title/the-case-of-langerhans-cell-histiocytosis-abt-letterer-siwe-disease-in-twin-girls
http://www.intechopen.com/articles/show/title/the-case-of-langerhans-cell-histiocytosis-abt-letterer-siwe-disease-in-twin-girls
