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Results: 6


Neurofibromin in neurofibromatosis type 1 - mutations in NF1gene as a cause of disease.

Abramowicz A, Gos M.

Dev Period Med. 2014 Jul-Sep;18(3):297-306. Review.


Renal artery stenosis due to neurofibromatosis type 1: case report and literature review.

Duan L, Feng K, Tong A, Liang Z.

Eur J Med Res. 2014 Mar 28;19:17. doi: 10.1186/2047-783X-19-17. Review.


Legius syndrome, an Update. Molecular pathology of mutations in SPRED1.

Brems H, Legius E.

Keio J Med. 2013;62(4):107-12. Epub 2013 Dec 10. Review.


McCune-Albright syndrome and the extraskeletal manifestations of fibrous dysplasia.

Collins MT, Singer FR, Eugster E.

Orphanet J Rare Dis. 2012 May 24;7 Suppl 1:S4. doi: 10.1186/1750-1172-7-S1-S4. Epub 2012 May 24. Review.


The melanogenesis and mechanisms of skin-lightening agents--existing and new approaches.

Gillbro JM, Olsson MJ.

Int J Cosmet Sci. 2011 Jun;33(3):210-21. doi: 10.1111/j.1468-2494.2010.00616.x. Epub 2011 Jan 25. Review.


A large intrathoracic meningocele in a patient with neurofibromatosis-1.

Jeong JW, Park KY, Yoon SM, Choe du W, Kim CH, Lee JC.

Korean J Intern Med. 2010 Jun;25(2):221-3. doi: 10.3904/kjim.2010.25.2.221. Epub 2010 Jun 1. Review.

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