113 related articles for article (PubMed ID: 20045924)
1. [Noonan syndrome: a case report and literature review].
Chen J; Yang Y; Tan Z; Wang Y; Tang X; Gong Y
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2009 Dec; 34(12):1261-5. PubMed ID: 20045924
[No Abstract] [Full Text] [Related]
2. [Mutation analysis of PTPN11 gene in Noonan syndrome].
Yang T; Meng Y; Shi HP; Zhao SM; Wang G; Huang SZ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):554-8. PubMed ID: 20931536
[TBL] [Abstract][Full Text] [Related]
3. Noonan syndrome: prenatal diagnosis in a woman carrying a PTPN11 gene mutation.
González-Huerta NC; Valdés-Miranda JM; Pérez-Cabrera A; Pacheco-Cuellar G; González-Huerta LM; Cuevas-Covarrubias SA
J Matern Fetal Neonatal Med; 2010 Jul; 23(7):688-91. PubMed ID: 20064076
[TBL] [Abstract][Full Text] [Related]
4. The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.
Sznajer Y; Keren B; Baumann C; Pereira S; Alberti C; Elion J; Cavé H; Verloes A
Pediatrics; 2007 Jun; 119(6):e1325-31. PubMed ID: 17515436
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Coinheritance of Noonan syndrome and Becker muscular dystrophy.
Dinopoulos A; Papadopoulou A; Manta P; Kekou K; Kanelopoulos T; Fretzayas A; Kitsiou S
Neuromuscul Disord; 2010 Jan; 20(1):61-3. PubMed ID: 19875288
[TBL] [Abstract][Full Text] [Related]
8. A mother and son with Noonan syndrome resulting from a PTPN11 mutation: first report of molecularly proven cases from Turkey.
Demir K; Yntema HG; Altincik A; Böber E
Turk J Pediatr; 2010; 52(3):321-4. PubMed ID: 20718194
[TBL] [Abstract][Full Text] [Related]
9. Bilateral cochlear implantation in children with Noonan syndrome.
Scheiber C; Hirschfelder A; Gräbel S; Peters H; Olze H
Int J Pediatr Otorhinolaryngol; 2009 Jun; 73(6):889-94. PubMed ID: 19303148
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Noonan syndrome with atrial septal defect and hypertrophic cardiomyopathy].
Nakayama M; Itou T; Abe T; Yamana T; Kawamura A; Yoshizumi T; Sunada M
Kyobu Geka; 2009 Jul; 62(7):535-7. PubMed ID: 19588822
[TBL] [Abstract][Full Text] [Related]
12. Double-chambered right ventricle in an adult with Noonan syndrome.
Patel AM; Kim JB; Roberts AE; Aragam J
Cardiol Rev; 2006; 14(5):e16-20. PubMed ID: 16924159
[TBL] [Abstract][Full Text] [Related]
13. Granular cell tumor of the scrotum in a child with Noonan syndrome.
Sidwell RU; Rouse P; Owen RA; Green JS
Pediatr Dermatol; 2008; 25(3):341-3. PubMed ID: 18577039
[TBL] [Abstract][Full Text] [Related]
14. Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors.
Mutesa L; Pierquin G; Janin N; Segers K; Thomée C; Provenzi M; Bours V
Cancer Genet Cytogenet; 2008 Apr; 182(1):40-2. PubMed ID: 18328949
[TBL] [Abstract][Full Text] [Related]
15. [Genetic identification of a case of Noonan syndrome and treatment with growth hormone].
Pi G; Zúñiga A; Gastaldo E; Ortiz M
Med Clin (Barc); 2014 Apr; 142(8):378-9. PubMed ID: 24054841
[No Abstract] [Full Text] [Related]
16. [New findings in Noonan syndrome and Leopard syndrome: activating mutations in RAF-1 and SOS-1].
Dereure O
Ann Dermatol Venereol; 2008; 135(8-9):624-5. PubMed ID: 18789305
[No Abstract] [Full Text] [Related]
17. Noonan syndrome associated with systemic lupus erythematosus.
Lisbona MP; Moreno M; Orellana C; Gratacos J; Larrosa M
Lupus; 2009 Mar; 18(3):267-9. PubMed ID: 19213867
[TBL] [Abstract][Full Text] [Related]
18. Pilocytic astrocytoma in a child with Noonan syndrome.
Schuettpelz LG; McDonald S; Whitesell K; Desruisseau DM; Grange DK; Gurnett CA; Wilson DB
Pediatr Blood Cancer; 2009 Dec; 53(6):1147-9. PubMed ID: 19621452
[TBL] [Abstract][Full Text] [Related]
19. High resolution melting analysis for mutation detection for PTPN11 gene: applications of this method for diagnosis of Noonan syndrome.
Lo FS; Luo JD; Lee YJ; Shu SG; Kuo MT; Chiou CC
Clin Chim Acta; 2009 Nov; 409(1-2):75-7. PubMed ID: 19737548
[TBL] [Abstract][Full Text] [Related]
20. Growth hormone and the heart in Noonan syndrome.
Noordam C
Horm Res; 2009 Dec; 72 Suppl 2():49-51. PubMed ID: 20029238
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
