Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Simon Paine"'
Publikováno v:
Paediatrics and Child Health. 32:339-350
Autor:
Ashwin Kumaria, Forsan Jahshan, Simon Paine, Malcolm Reed, Harshal A. Ingale, Yujay Ramakrishnan
Publikováno v:
British journal of neurosurgery.
Olfactory neuroblastoma (ONB) is a rare tumour of the skull base, typically originating from the nasal cavity and around the cribriform plate. We present the rare case of ONB originating from and limited to the sphenoid sinus in a 42-year old lady. P
Publikováno v:
Acta neurochirurgica. 164(2)
Beckwith-Wiedemann syndrome (BWS) is a rare congenital overgrowth syndrome associated with certain childhood tumours. We present the case of a 36-year-old lady with BWS who developed a left frontoinsular secondary glioblastoma. This is the first case
Autor:
Chelsea Spanoudakis, Rebecca Chapman, Simon Paine, Richard Grundy, Hester Franks, Timothy Ritzmann
Publikováno v:
Neuro-Oncology. 24:i39-i39
PURPOSE: Paediatric ependymoma is associated with dismal outcomes. Whilst understanding of its underlying biology has advanced, there has been little progress in treatment and clinical outcomes. Acting through four G protein-coupled receptors (encode
Autor:
Andrea Griesinger, Kent Riemondy, Nithyashri Eswaran, Andrew Donson, Nicholas Willard, Simon Paine, Georgia Bowes, John Rheaume, Rebecca Chapman, Judith Ramage, Andrew Jackson, Richard Grundy, Nicholas Foreman, Timothy Ritzmann
Publikováno v:
Neuro-Oncology. 24:i83-i83
Molecular profiling of pediatric ependymoma (EPN) has previously identified discrete neoplastic subpopulations, of which Mesenchymal EPN Cells (MEC) characterize Posterior Fossa A tumors (PFA). MECs are associated with tumor immunosuppression. Here w
Autor:
Jeffrey S. Pawlikowski, Claire Brock, Sheau-Chiann Chen, Lara Al-Olabi, Colin Nixon, Fiona McGregor, Simon Paine, Estelle Chanudet, Wendy Lambie, William M. Holmes, James M. Mullin, Ann Richmond, Hong Wu, Karen Blyth, Ayala King, Veronica A. Kinsler, Peter D. Adams
Publikováno v:
The Journal of Investigative Dermatology
Congenital melanocytic nevus (CMN) syndrome is the association of pigmented melanocytic nevi with extra-cutaneous features, classically melanotic cells within the central nervous system, most frequently caused by a mutation of NRAS codon 61. This con
Publikováno v:
Biochemical Society Transactions; Aug2011, Vol. 39 Issue 4, p917-919, 3p