200 related articles for article (PubMed ID: 10051160)
1. Severe Lhermitte-Duclos disease with unique germline mutation of PTEN.
Sutphen R; Diamond TM; Minton SE; Peacocke M; Tsou HC; Root AW
Am J Med Genet; 1999 Feb; 82(4):290-3. PubMed ID: 10051160
[TBL] [Abstract][Full Text] [Related]
2. A heterozygous frameshift mutation of the PTEN/MMAC1 gene in a patient with Lhermitte-Duclos disease - only the mutated allele was expressed in the cerebellar tumor.
Iida S; Tanaka Y; Fujii H; Hayashi S; Kimura M; Nagareda T; Moriwaki K
Int J Mol Med; 1998 Jun; 1(6):925-9. PubMed ID: 9852626
[TBL] [Abstract][Full Text] [Related]
3. Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
Zhou XP; Marsh DJ; Morrison CD; Chaudhury AR; Maxwell M; Reifenberger G; Eng C
Am J Hum Genet; 2003 Nov; 73(5):1191-8. PubMed ID: 14566704
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bones.
Delatycki MB; Danks A; Churchyard A; Zhou XP; Eng C
J Med Genet; 2003 Aug; 40(8):e92. PubMed ID: 12920084
[No Abstract] [Full Text] [Related]
8. Lhermitte-Duclos disease as a component of Cowden's syndrome. Case report and review of the literature.
Koch R; Scholz M; Nelen MR; Schwechheimer K; Epplen JT; Harders AG
J Neurosurg; 1999 Apr; 90(4):776-9. PubMed ID: 10193626
[TBL] [Abstract][Full Text] [Related]
9. Lhermitte-Duclos disease and Cowden disease: clinical and genetic study in five patients with Lhermitte-Duclos disease and literature review.
Pérez-Núñez A; Lagares A; Benítez J; Urioste M; Lobato RD; Ricoy JR; Ramos A; González P
Acta Neurochir (Wien); 2004 Jul; 146(7):679-90. PubMed ID: 15197611
[TBL] [Abstract][Full Text] [Related]
10. Lhermitte-Duclos disease: a report of 31 cases with immunohistochemical analysis of the PTEN/AKT/mTOR pathway.
Abel TW; Baker SJ; Fraser MM; Tihan T; Nelson JS; Yachnis AT; Bouffard JP; Mena H; Burger PC; Eberhart CG
J Neuropathol Exp Neurol; 2005 Apr; 64(4):341-9. PubMed ID: 15835270
[TBL] [Abstract][Full Text] [Related]
11. Germline PTEN mutations in three families with Cowden syndrome.
Celebi JT; Ping XL; Zhang H; Remington T; Sulica VI; Tsou HC; Peacocke M
Exp Dermatol; 2000 Apr; 9(2):152-6. PubMed ID: 10772390
[TBL] [Abstract][Full Text] [Related]
12. Cowden syndrome and the associated Lhermitte-Duclos disease--Case presentation.
Stępniak I; Trojanowski T; Drelich-Zbroja A; Willems P; Zaremba J
Neurol Neurochir Pol; 2015; 49(5):339-43. PubMed ID: 26377987
[TBL] [Abstract][Full Text] [Related]
13. Dysplastic gangliocytoma (Lhermitte-Duclos disease) associated with Cowden disease: report of a case and review of the literature for the genetic relationship between the two diseases.
Murata J; Tada M; Sawamura Y; Mitsumori K; Abe H; Nagashima K
J Neurooncol; 1999 Jan; 41(2):129-36. PubMed ID: 10222433
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Lhermitte-Duclos Disease in association with Cowden Syndrome.
Nielson C; Fischer T; Fischer R; Donald J; Rajpara A
Dermatol Online J; 2016 May; 22(5):. PubMed ID: 27617518
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.
Liaw D; Marsh DJ; Li J; Dahia PL; Wang SI; Zheng Z; Bose S; Call KM; Tsou HC; Peacocke M; Eng C; Parsons R
Nat Genet; 1997 May; 16(1):64-7. PubMed ID: 9140396
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]