105 related articles for article (PubMed ID: 16817452)
1. [Noonan syndrome].
Ogata T
Nihon Rinsho; 2006 Jun; Suppl 2():505-10. PubMed ID: 16817452
[No Abstract] [Full Text] [Related]
2. Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation.
Matsubara K; Yabe H; Ogata T; Yoshida R; Fukaya T
Am J Hematol; 2005 Jun; 79(2):171-2. PubMed ID: 15929108
[No Abstract] [Full Text] [Related]
3. Acute lymphoblastic leukaemia in Noonan syndrome.
Roti G; La Starza R; Ballanti S; Crescenzi B; Romoli S; Foá R; Tartaglia M; Aversa F; Fabrizio Martelli M; Mecucci C
Br J Haematol; 2006 May; 133(4):448-50. PubMed ID: 16643459
[No Abstract] [Full Text] [Related]
4. PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndrome.
Binder G; Neuer K; Ranke MB; Wittekindt NE
J Clin Endocrinol Metab; 2005 Sep; 90(9):5377-81. PubMed ID: 15985475
[TBL] [Abstract][Full Text] [Related]
5. Severe aortic valvar stenosis in familial Noonan syndrome with mutation of the PTPN11 gene.
Abadir S; Edouard T; Julia S
Cardiol Young; 2007 Feb; 17(1):95-7. PubMed ID: 17184563
[TBL] [Abstract][Full Text] [Related]
6. Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism.
Jafarov T; Ferimazova N; Reichenberger E
Clin Genet; 2005 Aug; 68(2):190-1. PubMed ID: 15996221
[No Abstract] [Full Text] [Related]
7. The first Noonan syndrome gene: PTPN11, which encodes the protein tyrosine phosphatase SHP-2.
Allanson J
Pediatr Res; 2002 Oct; 52(4):471. PubMed ID: 12357036
[No Abstract] [Full Text] [Related]
8. PTPN11 mutation in a young man with Noonan syndrome and retinitis pigmentosa.
Schollen E; Matthijs G; Fryns JF
Genet Couns; 2003; 14(2):259. PubMed ID: 12872825
[No Abstract] [Full Text] [Related]
9. Novel mitochondrial DNA mutations implicated in Noonan syndrome.
Dhandapany PS; Sadayappan S; Vanniarajan A; Karthikeyan B; Nagaraj C; Gowrishankar K; Selvam GS; Singh L; Thangaraj K
Int J Cardiol; 2007 Aug; 120(2):284-5. PubMed ID: 17092585
[TBL] [Abstract][Full Text] [Related]
10. PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes.
Ogata T; Yoshida R
Pediatr Endocrinol Rev; 2005 Jun; 2(4):669-74. PubMed ID: 16208280
[TBL] [Abstract][Full Text] [Related]
11. Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome.
Karow A; Steinemann D; Göhring G; Hasle H; Greiner J; Harila-Saari A; Flotho C; Zenker M; Schlegelberger B; Niemeyer CM; Kratz CP
Leukemia; 2007 Jun; 21(6):1303-5. PubMed ID: 17361219
[No Abstract] [Full Text] [Related]
12. Mutation analysis of PTPN11 in Noonan syndrome by WAVE.
Elanko N; Jeffery S
Methods Mol Med; 2006; 126():97-111. PubMed ID: 16930008
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Mild variable Noonan syndrome in a family with a novel PTPN11 mutation.
Zenker M; Voss E; Reis A
Eur J Med Genet; 2007; 50(1):43-7. PubMed ID: 17052965
[TBL] [Abstract][Full Text] [Related]
16. PTPN11 (protein tyrosine phosphatase, nonreceptor type 11) mutations and response to growth hormone therapy in children with Noonan syndrome.
Ferreira LV; Souza SA; Arnhold IJ; Mendonca BB; Jorge AA
J Clin Endocrinol Metab; 2005 Sep; 90(9):5156-60. PubMed ID: 15956085
[TBL] [Abstract][Full Text] [Related]
17. [Clinical symptoms and molecular pathogenesis of Noonan syndrome--current concepts].
Klapecki J; Obersztyn E; Laniewski-Wollk M; Szpecht-Potocka A; Mazurczak T
Med Wieku Rozwoj; 2006; 10(1 Pt 2):289-308. PubMed ID: 17028394
[TBL] [Abstract][Full Text] [Related]
18. PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning.
Schollen E; Matthijs G; Gewillig M; Fryns JP; Legius E
Eur J Hum Genet; 2003 Jan; 11(1):85-8. PubMed ID: 12529711
[TBL] [Abstract][Full Text] [Related]
19. Germline KRAS mutations cause Noonan syndrome.
Schubbert S; Zenker M; Rowe SL; Böll S; Klein C; Bollag G; van der Burgt I; Musante L; Kalscheuer V; Wehner LE; Nguyen H; West B; Zhang KY; Sistermans E; Rauch A; Niemeyer CM; Shannon K; Kratz CP
Nat Genet; 2006 Mar; 38(3):331-6. PubMed ID: 16474405
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]