Allen CE, Parsons DW. Biological and clinical significance of somaticmutations in Langerhans cell histiocytosis and related histiocytic neoplasticdisorders. Hematology Am Soc Hematol Educ Program. 2015;2015:559-64. doi:10.1182/asheducation-2015.1.559. Review.
Aoki Y, Niihori T, Narumi Y, Kure S, Matsubara Y. The RAS/MAPK syndromes:novel roles of the RAS pathway in human genetic disorders. Hum Mutat. 2008Aug;29(8):992-1006. doi: 10.1002/humu.20748. Review.
Bosco J, Allende A, Varikatt W, Lee R, Stewart GJ. Does the BRAF(V600E)mutation herald a new treatment era for Erdheim-Chester disease? A case-basedreview of a rare and difficult to diagnose disorder. Intern Med J. 2015Mar;45(3):348-51. doi: 10.1111/imj.12685. Review.
Campochiaro C, Tomelleri A, Cavalli G, Berti A, Dagna L. Erdheim-Chesterdisease. Eur J Intern Med. 2015 May;26(4):223-9. doi: 10.1016/j.ejim.2015.03.004.Epub 2015 Apr 10. Review.
Cives M, Simone V, Rizzo FM, Dicuonzo F, Cristallo Lacalamita M, Ingravallo G,Silvestris F, Dammacco F. Erdheim-Chester disease: a systematic review. Crit Rev Oncol Hematol. 2015 Jul;95(1):1-11. doi: 10.1016/j.critrevonc.2015.02.004. Epub2015 Feb 17. Review.
Dhomen N, Marais R. New insight into BRAF mutations in cancer. Curr Opin GenetDev. 2007 Feb;17(1):31-9. Review.
Gelb BD, Tartaglia M. Noonan Syndrome with Multiple Lentigines. 2007 Nov 30[updated 2015 May 14]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): Universityof Washington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1383/
Harmon CM, Brown N. Langerhans Cell Histiocytosis: A Clinicopathologic Review and Molecular Pathogenetic Update. Arch Pathol Lab Med. 2015 Oct;139(10):1211-4. doi: 10.5858/arpa.2015-0199-RA. Review.
Rauen KA. Cardiofaciocutaneous Syndrome. 2007 Jan 18 [updated 2016 Mar 3]. In:Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A,editors. GeneReviews® [Internet]. Seattle (WA): University of Washington,Seattle; 1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1186/
Roden AC, Hu X, Kip S, Parrilla Castellar ER, Rumilla KM, Vrana JA, VassalloR, Ryu JH, Yi ES. BRAF V600E expression in Langerhans cell histiocytosis:clinical and immunohistochemical study on 25 pulmonary and 54 extrapulmonarycases. Am J Surg Pathol. 2014 Apr;38(4):548-51. doi:10.1097/PAS.0000000000000129.
Rollins BJ. Genomic Alterations in Langerhans Cell Histiocytosis. HematolOncol Clin North Am. 2015 Oct;29(5):839-51. doi: 10.1016/j.hoc.2015.06.004.Review.
Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features,diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi:10.1542/peds.2009-3207. Epub 2010 Sep 27. Review.
Salgado CM, Basu D, Nikiforova M, Bauer BS, Johnson D, Rundell V, GrunwaldtLJ, Reyes-Múgica M. BRAF mutations are also associated with neurocutaneousmelanocytosis and large/giant congenital melanocytic nevi. Pediatr Dev Pathol.2015 Jan-Feb;18(1):1-9. doi: 10.2350/14-10-1566-OA.1. Epub 2014 Dec 9.
You are not a member of the advisory board for this topic. If you want to update advisory board member profile, please contact office@encyclopedia.pub.
OK
Confirm
Only members of the Encyclopedia advisory board for this topic are allowed to note entries. Would you like to become an advisory board member of the Encyclopedia?