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115. ALDH1A1 is a marker for acquired drug resistance in recurrent glioblastoma

126. Combined radiotherapy and concurrent tumor treating fields (TTFields) for glioblastoma: Dosimetric consequences on non-coplanar IMRT as initial results from a phase I trial

127. Catheter-associated meningitis in paediatric patients after brain surgery – incidence and risk factors

128. Current evidence for the application of blood-based biomarkers in high grade gliomas

129. Intra-arterial spasmolysis and angioplasty for treatment of cerebral vasospasm after subarachnoid haemorrhage

130. Ruptured middle cerebral artery aneurysms and the different bleeding patterns – influence of the sylvian fissure anatomy and geometric vascular parameters

131. Treatment algorithm for geriatric patients with acute subdural haematoma in neurological good condition – Is it always surgery?

132. BRAF mutation status and radiotherapy are prognostic factors in brain metastasis of malignant melanoma

133. PriCoTTF - eine Phase I/II Studie zu Tumortherapiefeldern vorausgehend und konkomitant zu Strahlentherapie und Temozolomid im neudiagnostizierten Glioblastom

134. Predictive value of glial fibrillary acid protein (GFAP) staining on survival of glioblastoma

135. The characteristics of cerebral aneurysms in young patients with tuberous sclerosis

136. Proposal on a novel biomarker panel for early diagnosis of delayed cerebral ischemia after subarachnoid haemorrhage

137. Wall enhancement patterns of thrombosed intracranial aneurysms in 7T MRI – insights into pathophysiology of aneurysm stability

138. Cervical spondylotic myelopathy – When should we operate?

139. Preoperative duration of symptoms is the most influential risk factor for treatment failure following microvascular decompression for trigeminal neuralgia

140. Cerebral cavernous malformations (CCM) – the second symptomatic haemorrhage – long-term follow-up

141. Automatic and efficient MRI-US segmentations for improving intraoperative image fusion in image-guided neurosurgery

145. Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia

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