Open Access
J Oral Med Oral Surg
Volume 28, Number 4, 2022
Article Number 47
Number of page(s) 4
Published online 21 December 2022
  1. Sinha SK, Diaz-Thomas A. Endocrinopathies Associated With Noonan Syndrome. In: Noonan Syndrome. Elsevier 2019. p. 49–60. [CrossRef] [Google Scholar]
  2. Lissewski C, Chune V, Pantaleoni F, De Luca A, Capri Y, Brinkmann J, et al. Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications. Eur J Hum Genet 2021;29:51–60. [CrossRef] [PubMed] [Google Scholar]
  3. Zadeh N. Noonan syndrome: phenotypic variations and molecular genetics. In: Noonan Syndrome. Elsevier 2019. p. 1–14. [Google Scholar]
  4. Reig I, Boixeda P, Fleta B, Morenoc C, Gámez L, Truchuelo M. Neurofibromatosis-Noonan syndrome: case report and clinicopathogenic review of the Neurofibromatosis-Noonan syndrome and RAS-MAPK pathway. Dermatol Online J 2011;17. [CrossRef] [Google Scholar]
  5. Tartaglia M, Gelb BD, Zenker M. Noonan syndrome and clinically related disorders. Best Pract Res Clin Endocrinol Metab 2011;25:161–179. [CrossRef] [PubMed] [Google Scholar]
  6. Tartaglia M, Zampino G, Gelb BD. Noonan syndrome: clinical aspects and molecular pathogenesis. Mol Syndromol 2010;1:2–26. [CrossRef] [PubMed] [Google Scholar]
  7. Friedrich RE, Scheuer HA. Sequential loss of mandibular permanent incisors in Noonan syndrome. In Vivo 2022;36:1021–1029. [CrossRef] [PubMed] [Google Scholar]
  8. Cordeddu V, Yin JC, Gunnarsson C, Virtanen C, Drunat S, Lepri F, et al. Activating mutations affecting the Dbl homology domain of SOS2 cause noonan syndrome. Hum Mutat 2015;36:1080–1087. [CrossRef] [PubMed] [Google Scholar]
  9. Lutz JC, Nicot R, Schlund M, Schaefer E, Bornert F, Fioretti F, et al. Dental and maxillofacial features of Noonan Syndrome: case series of ten patients. J Cranio-Maxillofac Surg 2020;48:242–250. [CrossRef] [Google Scholar]
  10. Noonan JA. Noonan syndrome and related disorders. Prog Pediatr Cardiol 2005;20:177–185. [CrossRef] [Google Scholar]
  11. Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, et al. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics 2010;126:746–759. [CrossRef] [PubMed] [Google Scholar]
  12. Zenker M, éditeur. Noonan syndrome and related disorders: a matter of deregulated ras signaling. Basel; New York: Karger 2009. 167 p. (Monographs in human genetics). [Google Scholar]
  13. Mahathi N. Inflammatory Pseudotumor and/or Xanthoma involving the maxilla and maxillary sinus: an unusual case report. Int J Dent Oral Sci 2021;2286–2290. [Google Scholar]
  14. Blessing K. Cutaneous granulomatous inflammation. Curr Diagn Pathol. 2005;11:219–235. [CrossRef] [Google Scholar]
  15. Olson NJ, Addante RR, de Abreu FB, Memoli VA. Central xanthoma of the jaw in association with Noonan syndrome. Hum Pathol 2018;82:202–205. [CrossRef] [PubMed] [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.