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Items: 1 to 20 of 217

1.

[Gardner fibroma: case report and discussion of a new soft tissue tumor entity].

Lanckohr C, Debiec-Rychter M, Müller O, Homann HH, Lehnhardt M, Herter P, Kuhnen C.

Pathologe. 2010 Mar;31(2):97-105. doi: 10.1007/s00292-009-1260-y. German.

PMID:
20063100
2.

Gardner fibroma: a clinicopathologic and immunohistochemical analysis of 45 patients with 57 fibromas.

Coffin CM, Hornick JL, Zhou H, Fletcher CD.

Am J Surg Pathol. 2007 Mar;31(3):410-6.

PMID:
17325483
3.
4.

Genetic testing for germline mutations of the APC gene in patients with apparently sporadic desmoid tumors but a family history of colorectal carcinoma.

Brueckl WM, Ballhausen WG, Förtsch T, Günther K, Fiedler W, Gentner B, Croner R, Boxberger F, Kirchner T, Hahn EG, Hohenberger W, Wein A.

Dis Colon Rectum. 2005 Jun;48(6):1275-81.

PMID:
15793634
5.

Novel germline APC mutations in Swedish patients with familial adenomatous polyposis and Gardner syndrome.

Nilbert M, Fernebro J, Kristoffersson U.

Scand J Gastroenterol. 2000 Nov;35(11):1200-3.

PMID:
11145293
6.

Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.

Eccles DM, van der Luijt R, Breukel C, Bullman H, Bunyan D, Fisher A, Barber J, du Boulay C, Primrose J, Burn J, Fodde R.

Am J Hum Genet. 1996 Dec;59(6):1193-201.

7.

Extra nuchal-type fibroma associated with elastosis, traumatic neuroma, a rare APC gene missense mutation, and a very rare MUTYH gene polymorphism: a case report and review of the literature*.

Linos K, Sedivcová M, Cerna K, Sima R, Kazakov DV, Nazeer T, Glazyrin A, Valerian BT, Carlson JA.

J Cutan Pathol. 2011 Nov;38(11):911-8. doi: 10.1111/j.1600-0560.2011.01745.x. Epub 2011 Jul 14. Review.

PMID:
21752055
8.

Identification of somatic APC mutations in recurrent desmoid tumors in a patient with familial adenomatous polyposis to determine actual recurrence of the original tumor or de novo occurrence.

Iwama T, Kuwabara K, Ushiama M, Yoshida T, Sugano K, Ishida H.

Fam Cancer. 2009;8(1):51-4. doi: 10.1007/s10689-008-9207-7. Epub 2008 Aug 15.

PMID:
18704758
9.

A germline mutation at the extreme 3' end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.

Couture J, Mitri A, Lagace R, Smits R, Berk T, Bouchard HL, Fodde R, Alman B, Bapat B.

Clin Genet. 2000 Mar;57(3):205-12.

PMID:
10782927
10.

A case of Gardner syndrome with a mutation at codon 1556 of APC: a suggested case of genotype-phenotype correlation in dental abnormality.

Oku T, Takayama T, Sato Y, Sato Y, Takada K, Hayashi T, Takahashi M, Kuroda M, Kato J, Niitsu Y.

Eur J Gastroenterol Hepatol. 2004 Jan;16(1):101-5.

PMID:
15095859
11.

A novel 3' mutation in the APC gene in a family presenting with a desmoid tumour.

Eccles D, Harvey J, Bateman A, Ross F.

J Med Genet. 2001 Dec;38(12):861-3. No abstract available.

12.

APC mutations in FAP-associated desmoid tumours are non-random but not 'just right'.

Latchford A, Volikos E, Johnson V, Rogers P, Suraweera N, Tomlinson I, Phillips R, Silver A.

Hum Mol Genet. 2007 Jan 1;16(1):78-82. Epub 2006 Nov 29.

PMID:
17135276
13.

Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2-year-old girl with familial adenomatous polyposis.

de Silva DC, Wright MF, Stevenson DA, Clark C, Gray ES, Holmes JD, Dean JC, Haites NE, Dunlop MG.

Cancer. 1996 Mar 1;77(5):972-6.

14.
15.

Multidisciplinary treatment of desmoid tumours in Gardner's syndrome due to a large interstitial deletion of chromosome 5q.

Casper M, Petek E, Henn W, Niewald M, Schneider G, Zimmer V, Lammert F, Raedle J.

QJM. 2014 Jul;107(7):521-7. doi: 10.1093/qjmed/hcu036. Epub 2014 Feb 18.

PMID:
24554300
16.

Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.

Scott RJ, Froggatt NJ, Trembath RC, Evans DG, Hodgson SV, Maher ER.

Hum Mol Genet. 1996 Dec;5(12):1921-4.

PMID:
8968744
17.

Multiple gynecologic tumors as rare associated phenotypes of FAP/Gardner syndrome in a family with the novel germline mutation in the APC gene.

Kovac M, Tomka M, Ciernikova S, Stevurkova V, Valachova A, Zajac V.

Clin Genet. 2006 Feb;69(2):183-6. No abstract available.

PMID:
16433700
18.

Coexistence of somatic and germ-line mutations of APC gene in desmoid tumors from patients with familial adenomatous polyposis.

Miyaki M, Konishi M, Kikuchi-Yanoshita R, Enomoto M, Tanaka K, Takahashi H, Muraoka M, Mori T, Konishi F, Iwama T.

Cancer Res. 1993 Nov 1;53(21):5079-82.

19.

Identification of Familial Adenomatous Polyposis carriers among children with desmoid tumours.

Kattentidt Mouravieva AA, Geurts-Giele IR, de Krijger RR, van Noesel MM, van de Ven CP, van den Ouweland AM, Kromosoeto JN, Dinjens WN, Dubbink HJ, Smits R, Wagner A.

Eur J Cancer. 2012 Aug;48(12):1867-74. doi: 10.1016/j.ejca.2012.01.004. Epub 2012 Feb 2.

PMID:
22305464
20.

Molecular nature of chromosome 5q loss in colorectal tumors and desmoids from patients with familial adenomatous polyposis.

Okamoto M, Sato C, Kohno Y, Mori T, Iwama T, Tonomura A, Miki Y, Utsunomiya J, Nakamura Y, White R, et al.

Hum Genet. 1990 Oct;85(6):595-9.

PMID:
2172153

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