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Nature Genetics|October 7, 2008
Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumorRichard H Scott, Jenny Douglas, Linda Baskcomb, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 27, 2022
Left-handedness should not be overrated as a risk factor for postoperative speech impairment in children after posterior fossa tumour surgery: a prospective European multicentre studyJonathan Kjær Grønbæk, Aske Foldbjerg Laustsen, Sebastian Toescu, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 2, 2012
Hyperfractionated versus conventional radiotherapy followed by chemotherapy in standard-risk medulloblastoma: results from the randomized multicenter HIT-SIOP PNET 4 trialBirgitta Lannering, Stefan Rutkowski, Francois Doz, et al.
Acta Neuropathologica|April 5, 2016
Risk stratification of childhood medulloblastoma in the molecular era: the current consensusVijay Ramaswamy, Marc Remke, Eric Bouffet, et al.
NMR in Biomedicine|February 2, 2024
Characterisation of paediatric brain tumours by their MRS metabolite profilesSimrandip K Gill, Heather E L Rose, Martin Wilson, et al.
Neuro-Oncology|July 29, 2024
SNO-EANO-EURACAN consensus on management of pineal parenchymal tumorsAnthony P Y Liu, Bryan K Li, Alexandre Vasiljevic, et al.
Oncotarget|April 4, 2012
Stratification of Wilms tumor by genetic and epigenetic analysisRichard H Scott, Anne Murray, Linda Baskcomb, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 11, 2025
Glucocorticoid use in paediatric posterior fossa tumour surgery and the occurrence of postoperative speech impairmentRebekka Sarup, Aske F Laustsen, Martin K Sørensen, et al.
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