๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Absence of FLT3 and JAK2 (V617F) mutations in Langerhans cell histiocytosis

โœ Scribed by Malak Abedalthagafi; Huimin Guo; Dan-Paul Hartmann; Metin Ozdemirli


Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
84 KB
Volume
33
Category
Article
ISSN
0145-2126

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Correlations of JAK2โ€“V617F mutation with
โœ Matthaios Speletas; Eirini Katodritou; Chrisoula Daiou; Eudokia Mandala; Emmanou ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 212 KB

Recently, the acquired mutation JAK2-V617F has been described in the majority of patients with myeloproliferative disorders (MPDs). In this study we evaluated its clinical and laboratory correlates in 166 patients with MPDs. The mutation was detected by allele-specific PCR in 119 patients: 81.4% (35

Use of indomethacin in Langerhans cell h
โœ Munn, Stephanie E.; Olliver, Lucy; Broadbent, Valerie; Pritchard, Jon ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 53 KB ๐Ÿ‘ 2 views

Background. Because prostaglandin (PG) E2 has been identified in the bone lesions of Langerhans cell histiocytosis (LCH), we speculated that indomethacin, a potent PG inhibitor, may be useful in patients with symptomatic LCH involving the bony skeleton. Procedure. We used indomethacin to treat patie