151 related articles for article (PubMed ID: 11443851)
1. Hamartoma and lentiginosis syndromes: clinical and molecular aspects.
Marsh DJ; Stratakis CA
Front Horm Res; 2001; 28():167-213. PubMed ID: 11443851
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.
Marsh DJ; Coulon V; Lunetta KL; Rocca-Serra P; Dahia PL; Zheng Z; Liaw D; Caron S; Duboué B; Lin AY; Richardson AL; Bonnetblanc JM; Bressieux JM; Cabarrot-Moreau A; Chompret A; Demange L; Eeles RA; Yahanda AM; Fearon ER; Fricker JP; Gorlin RJ; Hodgson SV; Huson S; Lacombe D; Eng C
Hum Mol Genet; 1998 Mar; 7(3):507-15. PubMed ID: 9467011
[TBL] [Abstract][Full Text] [Related]
4. Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.
Zhou X; Hampel H; Thiele H; Gorlin RJ; Hennekam RC; Parisi M; Winter RM; Eng C
Lancet; 2001 Jul; 358(9277):210-1. PubMed ID: 11476841
[TBL] [Abstract][Full Text] [Related]
5. PTEN: one gene, many syndromes.
Eng C
Hum Mutat; 2003 Sep; 22(3):183-98. PubMed ID: 12938083
[TBL] [Abstract][Full Text] [Related]
6. Genital lentigines in a 6-year-old boy with a family history of Cowden's disease: clinical and genetic evidence of the linkage between Bannayan-Riley-Ruvacalba syndrome and Cowden's disease.
Blum RR; Rahimizadeh A; Kardon N; Lebwohl M; Wei H
J Cutan Med Surg; 2001; 5(3):228-30. PubMed ID: 11685670
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN.
Celebi JT; Tsou HC; Chen FF; Zhang H; Ping XL; Lebwohl MG; Kezis J; Peacocke M
J Med Genet; 1999 May; 36(5):360-4. PubMed ID: 10353779
[TBL] [Abstract][Full Text] [Related]
8. PTEN hamartoma tumour syndrome: variability of an entity.
Merks JH; de Vries LS; Zhou XP; Nikkels P; Barth PG; Eng C; Hennekam RC
J Med Genet; 2003 Oct; 40(10):e111. PubMed ID: 14569134
[No Abstract] [Full Text] [Related]
9. Constipation, polyps, or cancer? Let PTEN predict your future.
Eng C
Am J Med Genet A; 2003 Nov; 122A(4):315-22. PubMed ID: 14518069
[TBL] [Abstract][Full Text] [Related]
10. [Cowden disease and the PTEN gene: a successfully clinical and biological combined approach].
Longy M
Bull Cancer; 2001 Dec; 88(12):1153-8. PubMed ID: 11792608
[TBL] [Abstract][Full Text] [Related]
11. Germline PTEN mutations in Cowden syndrome-like families.
Marsh DJ; Dahia PL; Caron S; Kum JB; Frayling IM; Tomlinson IP; Hughes KS; Eeles RA; Hodgson SV; Murday VA; Houlston R; Eng C
J Med Genet; 1998 Nov; 35(11):881-5. PubMed ID: 9832031
[TBL] [Abstract][Full Text] [Related]
12. Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome.
Pilarski R; Eng C
J Med Genet; 2004 May; 41(5):323-6. PubMed ID: 15121767
[No Abstract] [Full Text] [Related]
13. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.
Sweet K; Willis J; Zhou XP; Gallione C; Sawada T; Alhopuro P; Khoo SK; Patocs A; Martin C; Bridgeman S; Heinz J; Pilarski R; Lehtonen R; Prior TW; Frebourg T; Teh BT; Marchuk DA; Aaltonen LA; Eng C
JAMA; 2005 Nov; 294(19):2465-73. PubMed ID: 16287957
[TBL] [Abstract][Full Text] [Related]
14. Male breast cancer in Cowden syndrome patients with germline PTEN mutations.
Fackenthal JD; Marsh DJ; Richardson AL; Cummings SA; Eng C; Robinson BG; Olopade OI
J Med Genet; 2001 Mar; 38(3):159-64. PubMed ID: 11238682
[TBL] [Abstract][Full Text] [Related]
15. A 39-bp deletion polymorphism in PTEN in African American individuals: implications for molecular diagnostic testing.
Zhou XP; Hampel H; Roggenbuck J; Saba N; Prior TW; Eng C
J Mol Diagn; 2002 May; 4(2):114-7. PubMed ID: 11986403
[TBL] [Abstract][Full Text] [Related]
16. Identification of PTEN mutations in five families with Bannayan-Zonana syndrome.
Tok Celebi J; Chen FF; Zhang H; Ping XL; Tsou HC; Peacocke M
Exp Dermatol; 1999 Apr; 8(2):134-9. PubMed ID: 10232405
[TBL] [Abstract][Full Text] [Related]
17. Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.
Stratakis CA; Kirschner LS; Taymans SE; Tomlinson IP; Marsh DJ; Torpy DJ; Giatzakis C; Eccles DM; Theaker J; Houlston RS; Blouin JL; Antonarakis SE; Basson CT; Eng C; Carney JA
J Clin Endocrinol Metab; 1998 Aug; 83(8):2972-6. PubMed ID: 9709978
[TBL] [Abstract][Full Text] [Related]
18. Two novel mutations of PTEN gene in Japanese patients with Cowden syndrome.
Sawada T; Okada T; Miwa K; Satoh H; Asano A; Mabuchi H
Am J Med Genet A; 2004 Jul; 128A(1):12-4. PubMed ID: 15211648
[TBL] [Abstract][Full Text] [Related]
19. Recognition of genetic syndromes in families with suspected hereditary colon cancer syndromes.
Lindor NM
Clin Gastroenterol Hepatol; 2004 May; 2(5):366-75. PubMed ID: 15118973
[No Abstract] [Full Text] [Related]
20. Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis.
Zhou XP; Marsh DJ; Hampel H; Mulliken JB; Gimm O; Eng C
Hum Mol Genet; 2000 Mar; 9(5):765-8. PubMed ID: 10749983
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
