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Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|August 11, 2007
Papillary pineocytoma in child: a case reportWiesław Marcol, Katarzyna Kotulska, Wiesława Grajkowska, et al.
Neurosurgical Review|October 7, 2010
Childhood pineal parenchymal tumors: clinical and therapeutic aspectsMarek Mandera, Wiesław Marcol, Katarzyna Kotulska, et al.
Folia Neuropathologica|March 28, 2008
Expression of tuberin and hamartin in tuberous sclerosis complex-associated and sporadic cortical dysplasia of Taylor's balloon cell typeWiesława Grajkowska, Katarzyna Kotulska, Ewa Matyja, et al.
Pediatric Neurology|February 11, 2014
Surgical treatment of subependymal giant cell astrocytoma in tuberous sclerosis complex patientsKatarzyna Kotulska, Julita Borkowska, Marcin Roszkowski, et al.
Acta Neurochirurgica|December 6, 2022
External validation of the Ruptured Arteriovenous Malformation Grading Scale (RAGS) in a multicenter adult cohortLukasz Antkowiak, Marta Rogalska, Piotr Stogowski, et al.
Neurosurgical Focus|March 1, 2023
External validation of the Chicago Chiari Outcome Scale in adults with Chiari malformation type ILukasz Antkowiak, Piotr Stogowski, Tomasz Klepinowski, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 14, 2020
Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profileKrinio Giannikou, Zachary Zhu, Jaegil Kim, et al.
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