Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Samantha, Hettige"'
Autor:
Julia V. Cockle, Elizabeth A. Corley, Bassel Zebian, Samantha Hettige, Sucheta J. Vaidya, Paola Angelini, Joanna Stone, R Jane Leitch, Assunta Albanese, Henry C. Mandeville, Fernando Carceller, Lynley V. Marshall
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Pediatric diencephalic tumors represent a histopathologically and molecularly diverse group of neoplasms arising in the central part of the brain and involving eloquent structures, including the hypothalamic-pituitary axis (HPA), optic pathway, thala
Externí odkaz:
https://doaj.org/article/230517706a4040d5937a2e3f7c98238e
Publikováno v:
Acta Neurochirurgica. 165:351-354
Autor:
Simon Stapleton, Leslie R. Bridges, Francis G. Johnston, Anan Shtaya, Samantha Hettige, Robert Iorga
Publikováno v:
Neurosurgical Review. 45:103-118
Cauda equina paragangliomas are rare benign extra-adrenal neuroendocrine tumours arising from the neural crest cells associated with autonomic ganglia. These tumours are often mistaken preoperatively for ependymomas or schwannomas. Patients present w
Publikováno v:
Handbook of Pediatric Surgery ISBN: 9783030844660
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9ac2c0149d7154454564ff762b70dbc
https://doi.org/10.1007/978-3-030-84467-7_43
https://doi.org/10.1007/978-3-030-84467-7_43
Publikováno v:
Neurosurgery. 86:E98-E107
BACKGROUND Scalp cirsoid aneurysms are rare subcutaneous arteriovenous fistulae affecting the scalp. They can be easily misdiagnosed and mistreated. OBJECTIVE To review reported cases of scalp cirsoid aneurysms for their incidence, etiology, clinical
Autor:
Zita Reisz, Chris Jones, Lynley V. Marshall, Matthew Clarke, K. Powell, Danielle Martin, Komel Khabra, Joanna Stone, Sucheta Vaidya, Samantha Hettige, Leslie R. Bridges, Fernando Carceller, Janice Pearce, Safa Al-Sarraj, Istvan Bodi, Henry Mandeville, Henry Nanji, Bassel Zebian
Publikováno v:
Pediatric hematology and oncology. 38(8)
High grade gliomas (HGG) have a dismal prognosis with survival rates of 15-35%. Approximately 10-12% of pediatric HGG occur in young children and their molecular biology and clinical outcomes differ from those arising at older ages. We report on four
Autor:
Anan, Shtaya, Robert, Iorga, Samantha, Hettige, Leslie R, Bridges, Simon, Stapleton, Francis G, Johnston
Publikováno v:
Neurosurgical review. 45(1)
Cauda equina paragangliomas are rare benign extra-adrenal neuroendocrine tumours arising from the neural crest cells associated with autonomic ganglia. These tumours are often mistaken preoperatively for ependymomas or schwannomas. Patients present w
Autor:
Lynley V. Marshall, S. Stapleton, C. Chandler, Bassel Zebian, Sucheta Vaidya, F. Saran, Fernando Carceller, H. Mandeville, Joanna Stone, M. Bishr, Samantha Hettige, K. Powell
Publikováno v:
Radiotherapy and Oncology. 161:S1180-S1181
Autor:
Michael Farrell, Ketty Kessler, Jessica K.R. Boult, Safa Al-Sarraj, Fernando Carceller, Evelina Miele, Alan Mackay, Mariama Fofana, Leslie R. Bridges, Ranj Bhangoo, Rebecca Rogers, Paula Proszek, Lynley V. Marshall, Matthew Clarke, Janat Fazal Salom, Bassam Dabbous, Franco Locatelli, Christopher J. Lord, Chris Jones, Sucheta Vaidya, John Caird, Michelle Monje, Elisa Izquierdo, Angel M. Carcaboso, Andrea Carai, Samantha Hettige, Sara Temelso, Yura Grabovska, Christopher Chandler, Darach Crimmins, Lynn Bjerke, Simon R. Stapleton, Mara Vinci, Jane Pears, Angela Mastronuzzi, Giulia Pericoli, Kathryn R. Taylor, Elisabet F Potente, Simon P. Robinson, Anna Burford, Andrew J. Martin, Mike Hubank, Timothy E.G. Hassall, Bassel Zebian, Henry Mandeville, Jane Cryan, Helen N. Pemberton, Andrew S. Moore, Robert Johnston, Nagore G. Olaciregui, Valeria Molinari, Diana Carvalho
Paediatric high grade glioma and diffuse midline glioma (including DIPG) are comprised of multiple biological and clinical subgroups, the majority of which urgently require novel therapies. Patient-derivedin vitroprimary cell cultures represent poten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c89e3a42fb668fa43263a196c0ca138
https://doi.org/10.1101/2020.12.29.424674
https://doi.org/10.1101/2020.12.29.424674
Autor:
Verity Haffenden, RJ Paul Smith, Samantha Hettige, Sebastian Toescu, Kim Phipps, Kshitij Mankad, Christopher Clark, Richard Hayward, Kristian Aquilina
Publikováno v:
Child's Nervous System
Purpose To determine the value of structural magnetic resonance imaging (MRI) in predicting post-operative paediatric cerebellar mutism syndrome (pCMS) in children undergoing surgical treatment for medulloblastoma. Methods Retrospective cohort study