159 related articles for article (PubMed ID: 29848529)
1. Giant cell lesion of the jaw as a presenting feature of Noonan syndrome.
Sinnott BP; Patel M
BMJ Case Rep; 2018 May; 2018():. PubMed ID: 29848529
[TBL] [Abstract][Full Text] [Related]
2. Case report: Noonan-like multiple central giant cell granuloma syndrome.
Bitton N; Alexander S; Ruggiero S; Parameswaran A; Russo A; Ferguson F
Pediatr Dent; 2012; 34(5):144-7. PubMed ID: 23211900
[TBL] [Abstract][Full Text] [Related]
3. Differentiation of multiple giant cell lesions, Noonan-like syndrome, and (occult) hyperparathyroidism. Case report and review of the literature.
van Damme PA; Mooren RE
Int J Oral Maxillofac Surg; 1994 Feb; 23(1):32-6. PubMed ID: 8163857
[TBL] [Abstract][Full Text] [Related]
4. Bilateral central giant cell granulomas of the mandible in an 8-year-old girl with Noonan syndrome (Noonan-like/multiple giant cell lesion syndrome).
Edwards PC; Fox J; Fantasia JE; Goldberg J; Kelsch RD
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Mar; 99(3):334-40. PubMed ID: 15716842
[TBL] [Abstract][Full Text] [Related]
5. Blindness Secondary to Orbital Giant Cell Granuloma Mass-Effect in Noonan Syndrome With Return of Vision Following Surgical Decompression.
Anderson SR; Mancho SN
J Craniofac Surg; 2021 Sep; 32(6):e587-e589. PubMed ID: 34054099
[TBL] [Abstract][Full Text] [Related]
6. A case of neurofibromatosis-Noonan syndrome with a central giant cell granuloma.
Yazdizadeh M; Tapia JL; Baharvand M; Radfar L
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2004 Sep; 98(3):316-20. PubMed ID: 15356469
[TBL] [Abstract][Full Text] [Related]
7. Multiple central giant cell lesions with a Noonan-like phenotype.
Betts NJ; Stewart JC; Fonseca RJ; Scott RF
Oral Surg Oral Med Oral Pathol; 1993 Nov; 76(5):601-7. PubMed ID: 8247501
[TBL] [Abstract][Full Text] [Related]
8. Noonan-like/multiple giant cell lesion syndrome: report of a case and review of the literature.
Wolvius EB; de Lange J; Smeets EE; van der Wal KG; van den Akker HP
J Oral Maxillofac Surg; 2006 Aug; 64(8):1289-92. PubMed ID: 16860226
[No Abstract] [Full Text] [Related]
9. SOS1: a new player in the Noonan-like/multiple giant cell lesion syndrome.
Hanna N; Parfait B; Talaat IM; Vidaud M; Elsedfy HH
Clin Genet; 2009 Jun; 75(6):568-71. PubMed ID: 19438935
[TBL] [Abstract][Full Text] [Related]
10. Analysis of giant cell tumour of bone cells for Noonan syndrome/cherubism-related mutations.
Moskovszky L; Idowu B; Taylor R; Mertens F; Athanasou N; Flanagan A
J Oral Pathol Med; 2013 Jan; 42(1):95-8. PubMed ID: 22725657
[TBL] [Abstract][Full Text] [Related]
11. SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions.
Beneteau C; Cavé H; Moncla A; Dorison N; Munnich A; Verloes A; Leheup B
Eur J Hum Genet; 2009 Oct; 17(10):1216-21. PubMed ID: 19352411
[TBL] [Abstract][Full Text] [Related]
12. [Bilateral giant cell central granuloma of the jaws in a Noonan syndrome: About one case with emphasizing on bone giant cell lesions of the jaws].
Sizaret D; Tallegas M; de Pinieux G
Ann Pathol; 2022 Apr; 42(3):259-263. PubMed ID: 35058088
[TBL] [Abstract][Full Text] [Related]
13. Noonan syndrome associated with central giant cell granuloma.
Uçar B; Okten A; Mocan H; Erçin C
Clin Genet; 1998 May; 53(5):411-4. PubMed ID: 9660063
[TBL] [Abstract][Full Text] [Related]
14. Idiopathic bilateral central giant cell reparative granuloma of jaws: a case report and literature review.
Orhan E; Erol S; Deren O; Sevin A; Ekici O; Erdoğan B
Int J Pediatr Otorhinolaryngol; 2010 May; 74(5):547-52. PubMed ID: 20219254
[TBL] [Abstract][Full Text] [Related]
15. A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndrome.
Sarkozy A; Obregon MG; Conti E; Esposito G; Mingarelli R; Pizzuti A; Dallapiccola B
Eur J Hum Genet; 2004 Dec; 12(12):1069-72. PubMed ID: 15470362
[TBL] [Abstract][Full Text] [Related]
16. Extensive abdominal lipomatosis in a patient with Noonan/LEOPARD syndrome (Noonan syndrome-Multiple Lentigines).
Piard J; Verloes A; Cavé H; Peuchmaur M; Bennaceur S; Leheup B
Am J Med Genet A; 2012 Jun; 158A(6):1406-10. PubMed ID: 22528600
[TBL] [Abstract][Full Text] [Related]
17. Giant cell lesions in noonan syndrome: case report and review of the literature.
Bufalino A; Carrera M; Carlos R; Coletta RD
Head Neck Pathol; 2010 Jun; 4(2):174-7. PubMed ID: 20383758
[TBL] [Abstract][Full Text] [Related]
18. Atypical coronary artery aneurysms due to Kawasaki disease in Noonan syndrome with a novel PTPN11 mutation.
Takai S; Takasawa K; Doi S
Cardiol Young; 2019 Feb; 29(2):228-230. PubMed ID: 30511597
[TBL] [Abstract][Full Text] [Related]
19. Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutation.
Yoshida R; Ogata T; Masawa N; Nagai T
Pediatr Blood Cancer; 2008 Jun; 50(6):1274-6. PubMed ID: 18253957
[TBL] [Abstract][Full Text] [Related]
20. A mother and son with Noonan syndrome resulting from a PTPN11 mutation.
Derbent M
Turk J Pediatr; 2011; 53(1):117; author reply 118. PubMed ID: 21534355
[No Abstract] [Full Text] [Related]
[Next] [New Search]
