Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sara Barberan Martin"'
Autor:
Satyamaanasa Polubothu, Nicole Bender, Siobhan Muthiah, Davide Zecchin, Charalambos Demetriou, Sara Barberan Martin, Sony Malhotra, Jana Travnickova, Zhiqiang Zeng, Markus Böhm, Sebastien Barbarot, Catherine Cottrell, Olivia Davies, Eulalia Baselga, Nigel P. Burrows, Virginie Carmignac, Joey Santiago Diaz, Christine Fink, Holger A. Haenssle, Rudolf Happle, Mark Harland, Jacquelyn Majerowski, Pierre Vabres, Marie Vincent, Julia A. Newton-Bishop, D. Tim Bishop, Dawn Siegel, E. Elizabeth Patton, Maya Topf, Neil Rajan, Beth Drolet, Veronica A. Kinsler
Phakomatosis pigmentovascularis (PPV) is a diagnosis which denotes the coexistence of pigmentary and vascular birthmarks of specific types, accompanied by variable multisystem involvement including central nervous system disease, asymmetrical growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3d038bf38a83816c63d122330350c11
Autor:
Veronica Kinsler, Gavin Kelly, Neil Bulstrode, Pablo Lopez-Balboa, Alicia L. Bruzos, Satyamaanasa Polubothu, Sara Barberan Martin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04ab7ed8f85f3a0e95260a17a0991a88
https://doi.org/10.26226/m.62fa0098ba67fd001a9a091f
https://doi.org/10.26226/m.62fa0098ba67fd001a9a091f
Autor:
Davide Zecchin, Nicole Knoepfel, Anna Gluck, Mark Stevenson, Kate E. Lines, Satyamaanasa Polubothu, Noreen Muwanga-Nanyonjo, Sara Barberan-Martin, Fanourios Michailidis, Dale Bryant, Ulrike Loebel, Asuka Inoue, Robert Semple, Sarah Aylett, Rajesh V. Thakker, Veronica A. Kinsler
Publikováno v:
Cancer Research. 82:851-851
Background: Oncogenic variants of GNAQ and GNA11 arising in embryonic or fetal development lead to a spectrum of congenital mosaic disorders including Sturge-Weber syndrome (SWS) and Phakomatosis Pigmentovascularis (PPV). Both SWS and PPV are charact
Autor:
Sara Barberan Martin, Satyamaanasa Polubothu, Alicia Bruzos, Neil Bulstrode, Gavin Kelly, Veronica Kinsler
Publikováno v:
Cancer Research. 82:2014-2014
Congenital melanocytic naevi (CMN) are moles present at birth, and when multiple or very extensive can involve other organ systems as well as predisposing to melanoma. Some CMN patients develop a highly proliferative multinodular phenotype leading to
Autor:
D. Paige, Neil J. Sebire, Wei-Li Di, Iek Leng Cheng, Sara Barberan Martin, Connor Hughes, Satyamaanasa Polubothu, Karolina Gholam, Veronica A. Kinsler, Paulina Stadnik, Olumide Ogunbiyi, Alan Pittman, Melissa Riachi, Carolyn Charman
Publikováno v:
The Journal of Investigative Dermatology
No description supplied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a85d1bf57ebdc2711c44c784a218d34