Neurofibromatosis 1 (von Recklinghausen Disease)
Author:
Affiliation:
1. Division of Dermatology, Department of Medicine of Sensory and Motor Organs, Faculty of Medicine, Tottori University, Yonago, Japan
Publisher
Keio Journal of Medicine
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/kjm/advpub/0/advpub_2023-0013-IR/_pdf
Reference46 articles.
1. 1. Wilson BN, John AM, Handler MZ, Schwartz RA: Neurofibromatosis type 1: new developments in genetics and treatment. J Am Acad Dermatol 2021; 84: 1667–1676. PMID:32771543 https://doi.org/10.1016/j.jaad.2020.07.105
2. 2. Viskochil D, Buchberg AM, Xu G, Cawthon RM, Stevens J, Wolff RK, Culver M, Carey JC, Copeland NG, Jenkins NA, White R, O’Connell P: Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 1990; 62: 187–192. PMID:1694727 https://doi.org/10.1016/0092-8674(90)90252-A
3. 3. Lammert M, Friedman JM, Kluwe L, Mautner VF: Prevalence of neurofibromatosis 1 in German children at elementary school enrollment. Arch Dermatol 2005; 141: 71–74. PMID:15655144 https://doi.org/10.1001/archderm.141.1.71
4. 4. Yoshida Y, Ehara Y, Koga M, Imafuku S, Yamamoto O: Epidemiological analysis of major complications requiring medical intervention in patients with neurofibromatosis 1. Acta Derm Venereol 2018; 98: 753–756. PMID:29796689 https://doi.org/10.2340/00015555-2975
5. 5. Tanito K, Ota A, Kamide R, Nakagawa H, Niimura M: Clinical features of 58 Japanese patients with mosaic neurofibromatosis 1. J Dermatol 2014; 41: 724–728. PMID:25041723 https://doi.org/10.1111/1346-8138.12567
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