Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maureen McCalla"'
Autor:
Amy Gerrish, Chipo Mashayamombe-Wolfgarten, Edward Stone, Claudia Román-Montañana, Joseph Abbott, Helen Jenkinson, Gerard Millen, Sam Gurney, Maureen McCalla, Sarah-Jane Staveley, Anu Kainth, Maria Kirk, Claire Bowen, Susan Cavanagh, Sancha Bunstone, Megan Carney, Ajay Mohite, Samuel Clokie, M. Ashwin Reddy, Alison Foster, Stephanie Allen, Manoj Parulekar, Trevor Cole
Publikováno v:
Cancers, Vol 16, Iss 8, p 1565 (2024)
The identification of somatic RB1 variation is crucial to confirm the heritability of retinoblastoma. We and others have previously shown that, when tumour DNA is unavailable, cell-free DNA (cfDNA) derived from aqueous humour (AH) can be used to iden
Externí odkaz:
https://doaj.org/article/f4fb4a9adc374786bf15076a03be0d86
Autor:
Amy Gerrish, Benjamin Bowns, Chipo Mashayamombe-Wolfgarten, Elizabeth Young, Samantha Court, Joshua Bott, Maureen McCalla, Simon Ramsden, Michael Parks, David Goudie, Sue Carless, Samuel Clokie, Trevor Cole, Stephanie Allen
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 11, p 3517 (2020)
Retinoblastoma, the most common childhood eye cancer, presents in two forms: heritable or sporadic. Heritable retinoblastoma is caused by a germline mutation in the RB1 gene. Early diagnosis of children at risk of inheriting an RB1 mutation is crucia
Externí odkaz:
https://doaj.org/article/2891b0d63d1a4d40b326f0e819a75901
Autor:
Trevor Cole, Maureen McCalla, Benjamin Bowns, Elizabeth Young, Sue Carless, David Goudie, Samantha Court, Samuel Clokie, Simon C Ramsden, Stephanie Allen, Michael Parks, Chipo Mashayamombe-Wolfgarten, Amy Gerrish, Joshua Bott
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 11
Journal of Clinical Medicine, Vol 9, Iss 3517, p 3517 (2020)
Volume 9
Issue 11
Journal of Clinical Medicine, Vol 9, Iss 3517, p 3517 (2020)
Retinoblastoma, the most common childhood eye cancer, presents in two forms: heritable or sporadic. Heritable retinoblastoma is caused by a germline mutation in the RB1 gene. Early diagnosis of children at risk of inheriting an RB1 mutation is crucia
Autor:
Carol Hitchcott, John R Ainsworth, Trevor Cole, Manoj Parulekar, Maureen McCalla, Isabel Colmenero, Stephanie Allen, Amy Gerrish, Edward Stone, Samuel Clokie, Helen Jenkinson
Publikováno v:
The British Journal of Ophthalmology
Retinoblastoma is the most common eye malignancy in childhood caused by mutations in the RB1 gene. Both alleles of the RB1 gene must be mutated for tumour development. The initial RB1 mutation may be constitutional germline or somatic (originating in
Publikováno v:
Ophthalmic plastic and reconstructive surgery. 30(1)
Purpose Congenital anophthalmia and postenucleation socket contracture are difficult conditions that require serial socket expansion with the use of hydrogel expanders and custom-made conformers along with temporary tarsorrhaphy. Methods The authors
Publikováno v:
Retinoblastoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f157ab44f839776e84cafd90e9d358b
https://doi.org/10.5005/jp/books/11629_35
https://doi.org/10.5005/jp/books/11629_35