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Items: 1 to 20 of 119

1.

Two novel cases of trilateral retinoblastoma: genetics and review of the literature.

D'Elia G, Grotta S, Del Bufalo F, De Ioris MA, Surace C, Sirleto P, Romanzo A, Cozza R, Locatelli F, Angioni A.

Cancer Genet. 2013 Nov;206(11):398-401. doi: 10.1016/j.cancergen.2013.11.001. Epub 2013 Nov 19. Review.

PMID:
24412019
2.

Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.

Amare Kadam PS, Ghule P, Jose J, Bamne M, Kurkure P, Banavali S, Sarin R, Advani S.

Cancer Genet Cytogenet. 2004 Apr 1;150(1):33-43.

PMID:
15041221
3.

Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India.

Bamne MN, Ghule PN, Jose J, Banavali SD, Kurkure PA, Amare Kadam PS.

Genet Test. 2005 Fall;9(3):200-11.

PMID:
16225399
4.

Trilateral retinoblastoma with an RB1 deletion inherited from a carrier mother: a case report.

Amare P, Jose J, Chitalkar P, Kurkure P, Pai S, Nair C, Advani S.

Cancer Genet Cytogenet. 1999 May;111(1):28-31.

PMID:
10326587
5.

Baseline central nervous system magnetic resonance imaging in early detection of trilateral retinoblastoma: pitfalls in the diagnosis of pineal gland lesions.

De Ioris MA, Valente P, Randisi F, Buzzonetti L, Carai A, Cozza R, Del Bufalo F, Romanzo A, Angioni A, Cacchione A, Bernardi B, Mastronuzzi A.

Anticancer Res. 2014 Dec;34(12):7449-54.

PMID:
25503186
6.

RB1 germ-line deletions in Argentine retinoblastoma patients.

Fernández C, Repetto K, Dalamon V, Bergonzi F, Ferreiro V, Szijan I.

Mol Diagn Ther. 2007;11(1):55-61.

PMID:
17286450
7.

Fine mapping of whole RB1 gene deletions in retinoblastoma patients confirms PCDH8 as a candidate gene for psychomotor delay.

Castéra L, Dehainault C, Michaux D, Lumbroso-Le Rouic L, Aerts I, Doz F, Pelet A, Couturier J, Stoppa-Lyonnet D, Gauthier-Villars M, Houdayer C.

Eur J Hum Genet. 2013 Apr;21(4):460-4. doi: 10.1038/ejhg.2012.186. Epub 2012 Aug 22.

8.

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.

Abidi O, Knari S, Sefri H, Charif M, Senechal A, Hamel C, Rouba H, Zaghloul K, El Kettani A, Lenaers G, Barakat A.

Mol Vis. 2011;17:3541-7. Epub 2011 Dec 30.

10.

Retinoblastoma associated with chromosomal 13q14 deletion mosaicism.

Kivelä T, Tuppurainen K, Riikonen P, Vapalahti M.

Ophthalmology. 2003 Oct;110(10):1983-8. Review.

PMID:
14522775
11.

Ten novel RB1 gene mutations in patients with retinoblastoma.

Abouzeid H, Munier FL, Thonney F, Schorderet DF.

Mol Vis. 2007 Sep 19;13:1740-5.

PMID:
17960112
12.

RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients.

Dommering CJ, Mol BM, Moll AC, Burton M, Cloos J, Dorsman JC, Meijers-Heijboer H, van der Hout AH.

J Med Genet. 2014 Jun;51(6):366-74. doi: 10.1136/jmedgenet-2014-102264. Epub 2014 Mar 31.

PMID:
24688104
13.

Constitutional retinoblastoma gene deletion in Egyptian patients.

Mohammed AM, Kamel AK, Hammad SA, Afifi HH, El Sanabary Z, El Din ME.

World J Pediatr. 2009 Aug;5(3):222-5. doi: 10.1007/s12519-009-0042-1. Epub 2009 Aug 20.

PMID:
19693468
14.

Trilateral retinoblastoma.

Antoneli CB, Ribeiro Kde C, Sakamoto LH, Chojniak MM, Novaes PE, Arias VE.

Pediatr Blood Cancer. 2007 Mar;48(3):306-10. Review.

PMID:
16572402
15.

A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.

Parsam VL, Kannabiran C, Honavar S, Vemuganti GK, Ali MJ.

J Genet. 2009 Dec;88(4):517-27.

16.

Trilateral retinoblastoma: neuroimaging characteristics and value of routine brain screening on admission.

Rodjan F, de Graaf P, Brisse HJ, Göricke S, Maeder P, Galluzzi P, Aerts I, Alapetite C, Desjardins L, Wieland R, Popovic MB, Diezi M, Munier FL, Hadjistilianou T, Knol DL, Moll AC, Castelijns JA.

J Neurooncol. 2012 Sep;109(3):535-44. doi: 10.1007/s11060-012-0922-4. Epub 2012 Jul 18.

17.

Benign pineal cysts in children with bilateral retinoblastoma: a new variant of trilateral retinoblastoma?

Beck Popovic M, Balmer A, Maeder P, Braganca T, Munier FL.

Pediatr Blood Cancer. 2006 Jun;46(7):755-61.

PMID:
16003734
18.

Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.

Brichard B, Heusterspreute M, De Potter P, Chantrain C, Vermylen C, Sibille C, Gala JL.

Eur J Cancer. 2006 Jan;42(1):65-72.

PMID:
16343894
19.

Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing.

Chen Z, Moran K, Richards-Yutz J, Toorens E, Gerhart D, Ganguly T, Shields CL, Ganguly A.

Hum Mutat. 2014 Mar;35(3):384-91. doi: 10.1002/humu.22488. Epub 2013 Dec 20.

20.

Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma.

Grotta S, D'Elia G, Scavelli R, Genovese S, Surace C, Sirleto P, Cozza R, Romanzo A, De Ioris MA, Valente P, Tomaiuolo AC, Lepri FR, Franchin T, Ciocca L, Russo S, Locatelli F, Angioni A.

BMC Cancer. 2015 Nov 4;15:841. doi: 10.1186/s12885-015-1854-0.

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