Dual Effects of Resveratrol on the Expression and Secretion of Angiogenic Factors

por Kiamehr, Pegah, Shahidi, Minoo, Samii, Amir, Zaker, Farhad
Publicado 2022

Huge familial colloid cyst of the third ventricle: An extraordinary presentation

por Niknejad, Hamid Reza, Samii, Amir, Shen, Shang-Hang, Samii, Majid
Publicado 2015

Play it again, Sam: brain correlates of emotional music recognition

por Altenmüller, Eckart, Siggel, Susann, Mohammadi, Bahram, Samii, Amir, Münte, Thomas F.
Publicado 2014

IDH1 Mutation in Brain Stem Glioma: Case Report and Review of Literature

por Javadi, Seyed Amirhossein, Hartmann, Christian, Walter, Gerhard Franz, Banan, Roozbeh, Samii, Amir
Publicado 2018

Vestibular schwannoma surgery

por Link, Michael J., Yang, Isaac, Barker, Fred G., Samii, Amir, Theodosopoulos, Philip V.
Publicado 2021

MTHFR gene polymorphisms and susceptibility to myocardial infarction: Evidence from meta-analysis and trial sequential analysis

por Samii, Amir, Aslani, Saeed, Imani, Danyal, Razi, Bahman, Samaneh Tabaee, Seyedeh, Jamialahmadi, Tannaz, Sahebkar, Amirhossein
Publicado 2023

Observation of sonified movements engages a basal ganglia frontocortical network

por Schmitz, Gerd, Mohammadi, Bahram, Hammer, Anke, Heldmann, Marcus, Samii, Amir, Münte, Thomas F, Effenberg, Alfred O
Publicado 2013

Diffuse midline gliomas, H3 K27M-mutant are associated with less peritumoral edema and contrast enhancement in comparison to glioblastomas, H3 K27M-wildtype of midline structures

por Banan, Rouzbeh, Akbarian, Arash, Samii, Majid, Samii, Amir, Bertalanffy, Helmut, Lehmann, Ulrich, Hartmann, Christian, Brüning, Roland
Publicado 2021

Case of multifocal glioblastoma with four fusion transcripts of ALK, FGFR2, NTRK2, and NTRK3 genes stresses the need for tumor tissue multisampling for transcriptomic analysis

por Samii, Amir, Sorokin, Maxim, Kar, Souvik, Makovskaia, Luidmila, Garazha, Andrew, Hartmann, Christian, Moisseev, Aleksey, Kim, Ella, Giese, Alf, Buzdin, Anton
Publicado 2021

Differences in the MRI Signature and ADC Values of Diffuse Midline Gliomas with H3 K27M Mutation Compared to Midline Glioblastomas

por Raab, Peter, Banan, Rouzbeh, Akbarian, Arash, Esmaeilzadeh, Majid, Samii, Madjid, Samii, Amir, Bertalanffy, Helmut, Lehmann, Ulrich, Krauss, Joachim K., Lanfermann, Heinrich, Hartmann, Christian, Brüning, Roland
Publicado 2022

Identification of galectin-3 as a novel potential prognostic/predictive biomarker and therapeutic target for cerebral cavernous malformation disease

por Kar, Souvik, Perrelli, Andrea, Bali, Kiran Kumar, Mastrocola, Raffaella, Kar, Arpita, Khan, Bushra, Gand, Luis, Nayak, Arnab, Hartmann, Christian, Kunz, Wolfram S., Samii, Amir, Bertalanffy, Helmut, Retta, Saverio Francesco
Publicado 2023

Transcriptome-wide Profiling of Cerebral Cavernous Malformations Patients Reveal Important Long noncoding RNA molecular signatures

por Subhash, Santhilal, Kalmbach, Norman, Wegner, Florian, Petri, Susanne, Glomb, Torsten, Dittrich-Breiholz, Oliver, Huang, Caiquan, Bali, Kiran Kumar, Kunz, Wolfram S., Samii, Amir, Bertalanffy, Helmut, Kanduri, Chandrasekhar, Kar, Souvik
Publicado 2019

Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families

por Weber, Christine A. M., Krönke, Nicole, Volk, Valery, Auber, Bernd, Förster, Alisa, Trost, Detlef, Geffers, Robert, Esmaeilzadeh, Majid, Lalk, Michael, Nabavi, Arya, Samii, Amir, Krauss, Joachim K., Feuerhake, Friedrich, Hartmann, Christian, Wiese, Bettina, Brand, Frank, Weber, Ruthild G.
Publicado 2023

Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin

por Förster, Alisa, Brand, Frank, Banan, Rouzbeh, Hüneburg, Robert, Weber, Christine A. M., Ewert, Wiebke, Kronenberg, Jessica, Previti, Christopher, Elyan, Natalie, Beyer, Ulrike, Martens, Helge, Hong, Bujung, Bräsen, Jan H., Erbersdobler, Andreas, Krauss, Joachim K., Stangel, Martin, Samii, Amir, Wolf, Stephan, Preller, Matthias, Aretz, Stefan, Wiese, Bettina, Hartmann, Christian, Weber, Ruthild G.
Publicado 2021