6.
Kruse-Losler B, Diallo R, Gaertner C, Mischke K, Joos U, Kleinheinz J
. Central giant cell granuloma of the jaws: a clinical, radiologic, and histopathologic study of 26 cases. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006; 101(3):346-54.
DOI: 10.1016/j.tripleo.2005.02.060.
View
7.
Pogrel A
. The diagnosis and management of giant cell lesions of the jaws. Ann Maxillofac Surg. 2013; 2(2):102-6.
PMC: 3591058.
DOI: 10.4103/2231-0746.101325.
View
8.
Tosco P, Tanteri G, Iaquinta C, Fasolis M, Roccia F, Berrone S
. Surgical treatment and reconstruction for central giant cell granuloma of the jaws: a review of 18 cases. J Craniomaxillofac Surg. 2009; 37(7):380-7.
DOI: 10.1016/j.jcms.2009.04.002.
View
9.
Visnapuu V, Peltonen S, Tammisalo T, Peltonen J, Happonen R
. Radiographic findings in the jaws of patients with neurofibromatosis 1. J Oral Maxillofac Surg. 2011; 70(6):1351-7.
DOI: 10.1016/j.joms.2011.06.204.
View
10.
Chrcanovic B, Gomez R, Freire-Maia B
. Neurofibromatosis type 1 associated with bilateral central giant cell granuloma of the mandible. J Craniomaxillofac Surg. 2010; 39(7):538-43.
DOI: 10.1016/j.jcms.2010.10.014.
View
11.
Stewart D, Brems H, Gomes A, Ruppert S, Callens T, Williams J
. Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder. Genet Med. 2013; 16(6):448-59.
DOI: 10.1038/gim.2013.163.
View
12.
Darrigo Junior L, de Faria Ferraz V, Cormedi M, Araujo L, Magalhaes M, Carneiro R
. Epidemiological profile and clinical characteristics of 491 Brazilian patients with neurofibromatosis type 1. Brain Behav. 2022; 12(6):e2599.
PMC: 9226847.
DOI: 10.1002/brb3.2599.
View
13.
Jouhilahti E, Visnapuu V, Soukka T, Aho H, Peltonen S, Happonen R
. Oral soft tissue alterations in patients with neurofibromatosis. Clin Oral Investig. 2011; 16(2):551-8.
DOI: 10.1007/s00784-011-0519-x.
View
14.
Friedrich R, Scheuer H
. Non-odontogenic Intraosseous Radiolucent Lesions of the Mandibular Body Are Rare Findings on Panoramic Views of Patients With Neurofibromatosis Type 1. Anticancer Res. 2019; 39(4):1971-1985.
DOI: 10.21873/anticanres.13308.
View
15.
Mentzel H, Seidel J, Fitzek C, Eichhorn A, Vogt S, Reichenbach J
. Pediatric brain MRI in neurofibromatosis type I. Eur Radiol. 2004; 15(4):814-22.
DOI: 10.1007/s00330-004-2433-y.
View
16.
de Lange J, van den Akker H, van den Berg H
. Central giant cell granuloma of the jaw: a review of the literature with emphasis on therapy options. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007; 104(5):603-15.
DOI: 10.1016/j.tripleo.2007.04.003.
View
17.
DeBella K, Szudek J, Friedman J
. Use of the national institutes of health criteria for diagnosis of neurofibromatosis 1 in children. Pediatrics. 2000; 105(3 Pt 1):608-14.
DOI: 10.1542/peds.105.3.608.
View
18.
Salman M, Hossain S, Alqublan L, Bunge M, Rozovsky K
. Cerebellar radiological abnormalities in children with neurofibromatosis type 1: part 1 - clinical and neuroimaging findings. Cerebellum Ataxias. 2018; 5:14.
PMC: 6211433.
DOI: 10.1186/s40673-018-0093-y.
View
19.
Salman M, Hossain S, Gorun S, Alqublan L, Bunge M, Rozovsky K
. Cerebellar radiological abnormalities in children with neurofibromatosis type 1: part 2 - a neuroimaging natural history study with clinical correlations. Cerebellum Ataxias. 2018; 5:13.
PMC: 6208104.
DOI: 10.1186/s40673-018-0092-z.
View
20.
Friedrich R, Grob T, Hollants S, Zustin J, Spaepen M, Mautner V
. Recurrent multilocular mandibular giant cell granuloma in neurofibromatosis type 1: Evidence for second hit mutation of NF1 gene in the jaw lesion and treatment with curettage and bone substitute materials. J Craniomaxillofac Surg. 2016; 44(8):1054-60.
DOI: 10.1016/j.jcms.2016.05.010.
View