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Items: 1 to 20 of 74

1.

KCNQ1OT1 hypomethylation: a novel disguised genetic predisposition in sporadic pediatric adrenocortical tumors?

Wijnen M, Alders M, Zwaan CM, Wagner A, van den Heuvel-Eibrink MM.

Pediatr Blood Cancer. 2012 Sep;59(3):565-6. doi: 10.1002/pbc.23398.

PMID:
22610651
2.

Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome.

Alsultan A, Lovell MA, Hayes KL, Allshouse MJ, Garrington TP.

Pediatr Blood Cancer. 2008 Nov;51(5):695-8. doi: 10.1002/pbc.21694.

PMID:
18668518
3.

Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith-Wiedemann syndrome as a sporadic adrenocortical tumor.

H'mida Ben-Brahim D, Hammami S, Haddaji Mastouri M, Trabelsi S, Chourabi M, Sassi S, Mougou S, Gribaa M, Zakhama A, Guédiche MN, Saad A.

Appl Transl Genom. 2014 Oct 15;4:1-3. doi: 10.1016/j.atg.2014.10.001.

4.

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

Weksberg R, Nishikawa J, Caluseriu O, Fei YL, Shuman C, Wei C, Steele L, Cameron J, Smith A, Ambus I, Li M, Ray PN, Sadowski P, Squire J.

Hum Mol Genet. 2001 Dec 15;10(26):2989-3000.

5.

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.

Bliek J, Maas SM, Ruijter JM, Hennekam RC, Alders M, Westerveld A, Mannens MM.

Hum Mol Genet. 2001 Mar 1;10(5):467-76.

6.

Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.

Shuman C, Smith AC, Steele L, Ray PN, Clericuzio C, Zackai E, Parisi MA, Meadows AT, Kelly T, Tichauer D, Squire JA, Sadowski P, Weksberg R.

Am J Med Genet A. 2006 Jul 15;140(14):1497-503.

PMID:
16770802
7.

Late relapse of adrenocortical carcinoma in Beckwith-Wiedemann syndrome. Clinical, endocrinological and genetic aspects.

Hertel NT, Carlsen N, Kerndrup G, Pedersen IL, Clausen N, Hahnemann JM, Jacobsen BB.

Acta Paediatr. 2003 Apr;92(4):439-43.

PMID:
12801110
8.

The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndrome.

Cerrato F, Vernucci M, Pedone PV, Chiariotti L, Sebastio G, Bruni CB, Riccio A.

Hum Genet. 2002 Jul;111(1):105-7. No abstract available.

PMID:
12136243
9.

Pathogenesis of adrenocortical incidentalomas and genetic syndromes associated with adrenocortical neoplasms.

Gicquel C, Bertherat J, Le Bouc Y, Bertagna X.

Endocrinol Metab Clin North Am. 2000 Mar;29(1):1-13, vii. Review.

PMID:
10732260
10.

Expression of a high molecular weight form of insulin-like growth factor II in a Beckwith-Wiedemann syndrome associated adrenocortical adenoma.

Schofield PN, Nystrom A, Smith J, Spitz L, Grant D, Zapf J.

Cancer Lett. 1995 Jul 20;94(1):71-7.

PMID:
7621447
11.

Clonal composition of human adrenocortical neoplasms.

Beuschlein F, Reincke M, Karl M, Travis WD, Jaursch-Hancke C, Abdelhamid S, Chrousos GP, Allolio B.

Cancer Res. 1994 Sep 15;54(18):4927-32.

12.

Infantile adrenocortical tumor with an activating GNAS1 mutation.

Sidhu A, Debelenko L, Misra VK.

J Clin Endocrinol Metab. 2013 Jan;98(1):E115-8. doi: 10.1210/jc.2012-2933.

PMID:
23105121
13.

A unique case of synchronous functional adrenocortical adenoma and myelolipoma within the ectopic adrenal cortex in a child with Beckwith-Wiedemann syndrome.

Cardinalli IA, de Oliveira-Filho AG, Mastellaro MJ, Ribeiro RC, Aguiar SS.

Pathol Res Pract. 2012 Mar 15;208(3):189-94. doi: 10.1016/j.prp.2011.12.011.

PMID:
22309953
14.

Genetic background of adrenocortical tumor development.

Kjellman M, Larsson C, Bäckdahl M.

World J Surg. 2001 Jul;25(7):948-56. Review.

PMID:
11572037
15.

Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography.

Ma GC, Chang SD, Chang Y, Chang SP, Yang CW, Lee MJ, Lee TH, Chen M.

Fertil Steril. 2008 Oct;90(4):1279-82. doi: 10.1016/j.fertnstert.2007.10.075.

PMID:
18249379
16.

Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann-Beckwith syndrome.

Hayward NK, Little MH, Mortimer RH, Clouston WM, Smith PJ.

Cancer Genet Cytogenet. 1988 Jan;30(1):127-32.

PMID:
3275489
17.

Genetic aspects of adrenocortical tumours and hyperplasias.

Mazzuco TL, Durand J, Chapman A, Crespigio J, Bourdeau I.

Clin Endocrinol (Oxf). 2012 Jul;77(1):1-10. doi: 10.1111/j.1365-2265.2012.04403.x. Review.

PMID:
22471738
18.

Beckwith-Wiedemann syndrome.

Choufani S, Shuman C, Weksberg R.

Am J Med Genet C Semin Med Genet. 2010 Aug 15;154C(3):343-54. doi: 10.1002/ajmg.c.30267. Review.

PMID:
20803657
19.

The molecular genetics of adrenocortical carcinoma.

Barlaskar FM, Hammer GD.

Rev Endocr Metab Disord. 2007 Dec;8(4):343-8. Review. No abstract available.

PMID:
17934868
20.

Familial predisposition to adrenocortical tumors: clinical and biological features and management strategies.

Ribeiro RC, Pinto EM, Zambetti GP.

Best Pract Res Clin Endocrinol Metab. 2010 Jun;24(3):477-90. doi: 10.1016/j.beem.2010.03.002. Review.

PMID:
20833338
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