421 related articles for article (PubMed ID: 16061556)
1. Arteriovenous malformations in Cowden syndrome.
Turnbull MM; Humeniuk V; Stein B; Suthers GK
J Med Genet; 2005 Aug; 42(8):e50. PubMed ID: 16061556
[TBL] [Abstract][Full Text] [Related]
2. PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.
Piccione M; Fragapane T; Antona V; Giachino D; Cupido F; Corsello G
Am J Med Genet A; 2013 Nov; 161A(11):2902-8. PubMed ID: 24123798
[TBL] [Abstract][Full Text] [Related]
3. Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome.
Busa T; Milh M; Degardin N; Girard N; Sigaudy S; Longy M; Olshchwang S; Sobol H; Chabrol B; Philip N
Eur J Paediatr Neurol; 2015 Mar; 19(2):188-92. PubMed ID: 25549896
[TBL] [Abstract][Full Text] [Related]
4. Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome.
Zori RT; Marsh DJ; Graham GE; Marliss EB; Eng C
Am J Med Genet; 1998 Dec; 80(4):399-402. PubMed ID: 9856571
[TBL] [Abstract][Full Text] [Related]
5. Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features.
Pilarski R; Stephens JA; Noss R; Fisher JL; Prior TW
J Med Genet; 2011 Aug; 48(8):505-12. PubMed ID: 21659347
[TBL] [Abstract][Full Text] [Related]
6. The role of PTEN, a phosphatase gene, in inherited and sporadic nonmedullary thyroid tumors.
Eng C
Recent Prog Horm Res; 1999; 54():441-52; discussion 453. PubMed ID: 10548886
[TBL] [Abstract][Full Text] [Related]
7. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
Marsh DJ; Kum JB; Lunetta KL; Bennett MJ; Gorlin RJ; Ahmed SF; Bodurtha J; Crowe C; Curtis MA; Dasouki M; Dunn T; Feit H; Geraghty MT; Graham JM; Hodgson SV; Hunter A; Korf BR; Manchester D; Miesfeldt S; Murday VA; Nathanson KL; Parisi M; Pober B; Romano C; Eng C
Hum Mol Genet; 1999 Aug; 8(8):1461-72. PubMed ID: 10400993
[TBL] [Abstract][Full Text] [Related]
8. Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations.
Sherman SK; Maxwell JE; Qian Q; Bellizzi AM; Braun TA; Iannettoni MD; Darbro BW; Howe JR
Cancer Genet; 2015; 208(1-2):41-6. PubMed ID: 25554686
[TBL] [Abstract][Full Text] [Related]
9. Cowden disease and Lhermitte-Duclos disease: characterization of a new phakomatosis.
Robinson S; Cohen AR
Neurosurgery; 2000 Feb; 46(2):371-83. PubMed ID: 10690726
[TBL] [Abstract][Full Text] [Related]
10. Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delay.
Lynch NE; Lynch SA; McMenamin J; Webb D
Arch Dis Child; 2009 Jul; 94(7):553-4. PubMed ID: 19321504
[TBL] [Abstract][Full Text] [Related]
11. Analysis of PTEN gene mutations in Korean patients with Cowden syndrome and polyposis syndrome.
Kim DK; Myung SJ; Yang SK; Hong SS; Kim KJ; Byeon JS; Lee GH; Kim JH; Min YI; Lee SM; Jeong JY; Song K; Jung SA
Dis Colon Rectum; 2005 Sep; 48(9):1714-22. PubMed ID: 16007494
[TBL] [Abstract][Full Text] [Related]
12. Cutaneous lipoma in children: 5 cases with Bannayan-Riley-Ruvalcaba syndrome.
Buisson P; Leclair MD; Jacquemont S; Podevin G; Camby C; David A; Heloury Y
J Pediatr Surg; 2006 Sep; 41(9):1601-3. PubMed ID: 16952599
[TBL] [Abstract][Full Text] [Related]
13. Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
Longy M; Coulon V; Duboué B; David A; Larrègue M; Eng C; Amati P; Kraimps JL; Bottani A; Lacombe D; Bonneau D
J Med Genet; 1998 Nov; 35(11):886-9. PubMed ID: 9832032
[TBL] [Abstract][Full Text] [Related]
14. Cowden syndrome presenting as breast cancer: imaging and clinical features.
Seo M; Cho N; Ahn HS; Moon HG
Korean J Radiol; 2014; 15(5):586-90. PubMed ID: 25246819
[TBL] [Abstract][Full Text] [Related]
15. PTEN Mutation Identified in Patient Diagnosed with Simultaneous Multiple Cancers.
Won HS; Chang ED; Na SJ; Whang IY; Lee DS; You SH; Kim YS; Kim JS
Cancer Res Treat; 2019 Jan; 51(1):402-407. PubMed ID: 29510612
[TBL] [Abstract][Full Text] [Related]
16. Imaging of PTEN-related abnormalities in the central nervous system.
Dhamija R; Hoxworth JM
Clin Imaging; 2020 Apr; 60(2):180-185. PubMed ID: 31927175
[TBL] [Abstract][Full Text] [Related]
17. Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report.
Jenny B; Radovanovic I; Haenggeli CA; Delavelle J; Rüfenacht D; Kaelin A; Blouin JL; Bottani A; Rilliet B
J Neurosurg; 2007 Oct; 107(4 Suppl):307-13. PubMed ID: 17941496
[TBL] [Abstract][Full Text] [Related]
18. Cowden syndrome.
Gustafson S; Zbuk KM; Scacheri C; Eng C
Semin Oncol; 2007 Oct; 34(5):428-34. PubMed ID: 17920899
[TBL] [Abstract][Full Text] [Related]
19. Hemimegalencephaly with Bannayan-Riley-Ruvalcaba syndrome.
Ghusayni R; Sachdev M; Gallentine W; Mikati MA; McDonald MT
Epileptic Disord; 2018 Feb; 20(1):30-34. PubMed ID: 29444762
[TBL] [Abstract][Full Text] [Related]
20. Skin abnormalities in individuals with macrocephaly: Cowden disease from a dermatologist's point of view.
van der Velden JJ; Vreeburg M; Smeets EE; Schrander-Stumpel CT; van Steensel MA
Int J Dermatol; 2008 Nov; 47 Suppl 1():45-8. PubMed ID: 18986487
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
