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Pediatric Blood & Cancer|July 1, 2010
Fanconi anemia gene mutations are not involved in sporadic Wilms tumorMuriel A Adank, Heidi Segers, Saskia E van Mil, et al.
Acta Neuropathologica|November 4, 2019
Molecular characterization of histopathological ependymoma variantsJulia E Neumann, Michael Spohn, Denise Obrecht, et al.
European Journal of Pediatrics|September 4, 2023
Health-related quality of life in children with congenital vascular malformationsFrédérique C M Bouwman, Chris Verhaak, Ivo de Blaauw, et al.
Annals of Internal Medicine|March 21, 2007
Predicting intracranial traumatic findings on computed tomography in patients with minor head injury: the CHIP prediction ruleMarion Smits, Diederik W J Dippel, Ewout W Steyerberg, et al.
Annals of the Rheumatic Diseases|February 16, 2013
Measurement invariance of the Illness Invalidation Inventory (3*I) across language, rheumatic disease and genderMarianne Belia Kool, Rens van de Schoot, Isabel López-Chicheri García, et al.
Acta Neuropathologica|March 5, 2019
TCF4 (E2-2) harbors tumor suppressive functions in SHH medulloblastomaMalte Hellwig, Marlen C Lauffer, Michael Bockmayr, et al.
British Journal of Clinical Pharmacology|December 27, 2021
Effective low-dose sirolimus regimen for kaposiform haemangioendothelioma with Kasabach-Merritt phenomenon in young infantsVeroniek E M Harbers, Nathalie van der Salm, Sjoert A H Pegge, et al.
Brain Pathology (Zurich, Switzerland)|October 17, 2018
Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imagingMélanie Pagès, Kristian W Pajtler, Stéphanie Puget, et al.
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