Piebaldism and Neurofibromatosis Type 1: Horses of Very Different Colors
- 1 February 2004
- journal article
- review article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 122 (2)
- https://doi.org/10.1046/j.0022-202x.2004.22235.x
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Association of Piebaldism and Neurofibromatosis Type 1 in a GirlPediatric Dermatology, 2001
- Genetic and Biochemical Evidence That Haploinsufficiency of the Nf1 Tumor Suppressor Gene Modulates Melanocyte and Mast Cell Fates in VivoThe Journal of Experimental Medicine, 2000
- Expression of Kit in neurofibromin-deficient human Schwann cells: role in Schwann cell hyperplasia associated with Type 1 NeurofibromatosisOncogene, 1998
- The Diagnostic Evaluation and Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2JAMA, 1997
- Diagnosis of Neurofibromatosis by Cutaneous ExaminationSeminars in Neurology, 1992
- Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.Proceedings of the National Academy of Sciences, 1991
- Clinical Diagnosis of von Recklinghausen's NeurofibromatosisAnnals of the New York Academy of Sciences, 1986
- Congenital Circumscribed Hypomelanosis: A Characterization Based on Electron Microscopic Study of Tuberous Sclerosis, Nevus Depigmentosus, and PiebaldismJournal of Investigative Dermatology, 1975
- Ultrastructure of Giant Pigment Granules (Macromelanosomes) in the Cutaneous Pigmented Macules of NeurofibromatosisJournal of Investigative Dermatology, 1973
- Electron Microscopy of Melanocytes in Human Piebaldism*Journal of Investigative Dermatology, 1965