178 related articles for article (PubMed ID: 11332402)
1. The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome.
Parisi MA; Dinulos MB; Leppig KA; Sybert VP; Eng C; Hudgins L
J Med Genet; 2001 Jan; 38(1):52-8. PubMed ID: 11332402
[No 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. 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]
4. Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.
Hendriks YM; Verhallen JT; van der Smagt JJ; Kant SG; Hilhorst Y; Hoefsloot L; Hansson KB; van der Straaten PJ; Boutkan H; Breuning MH; Vasen HF; Bröcker-Vriends AH
Fam Cancer; 2003; 2(2):79-85. PubMed ID: 14574156
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations.
Dahia PM; Gimm O; Chi H; Marsh DJ; Reynolds PR; Eng C
J Med Genet; 2000 Sep; 37(9):715-7. PubMed ID: 11182934
[No Abstract] [Full Text] [Related]
8. A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association.
Reardon W; Zhou XP; Eng C
J Med Genet; 2001 Dec; 38(12):820-3. PubMed ID: 11748304
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Mutations of the human PTEN gene.
Bonneau D; Longy M
Hum Mutat; 2000; 16(2):109-22. PubMed ID: 10923032
[TBL] [Abstract][Full Text] [Related]
12. Germline mutations in the PTEN gene in Israeli patients with Bannayan-Riley-Ruvalcaba syndrome and women with familial breast cancer.
Figer A; Kaplan A; Frydman M; Lev D; Paswell J; Papa MZ; Goldman B; Friedman E
Clin Genet; 2002 Oct; 62(4):298-302. PubMed ID: 12372056
[TBL] [Abstract][Full Text] [Related]
13. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease.
Arch EM; Goodman BK; Van Wesep RA; Liaw D; Clarke K; Parsons R; McKusick VA; Geraghty MT
Am J Med Genet; 1997 Sep; 71(4):489-93. PubMed ID: 9286463
[TBL] [Abstract][Full Text] [Related]
14. PTEN: one gene, many syndromes.
Eng C
Hum Mutat; 2003 Sep; 22(3):183-98. PubMed ID: 12938083
[TBL] [Abstract][Full Text] [Related]
15. Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndrome.
Carethers JM; Furnari FB; Zigman AF; Lavine JE; Jones MC; Graham GE; Teebi AS; Huang HJ; Ha HT; Chauhan DP; Chang CL; Cavenee WK; Boland CR
Cancer Res; 1998 Jul; 58(13):2724-6. PubMed ID: 9661881
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]