Search Results - Blümcke, Ingmar
- Showing 1 - 7 results of 7
-
1
Anaplastic ganglioglioma: a diagnosis comprising several distinct tumour types : original article by Reinhardt, Annekathrin (Author) , Pfister, Kristin (Author) , Schrimpf, Daniel (Author) , Stichel, Damian (Author) , Sahm, Felix (Author) , Reuss, David (Author) , Capper, David (Author) , Wefers, Annika K. (Author) , Ebrahimi, Azadeh (Author) , Sill, Martin (Author) , Felsberg, Jörg (Author) , Reifenberger, Guido (Author) , Becker, Albert J. (Author) , Prinz, Marco (Author) , Staszewski, Ori (Author) , Hartmann, Christian (Author) , Schittenhelm, Jens Florian (Author) , Gramatzki, Dorothee (Author) , Weller, Michael (Author) , Olar, Adriana (Author) , Rushing, Elisabeth Jane (Author) , Bergmann, Markus (Author) , Farrell, Michael A. (Author) , Blümcke, Ingmar (Author) , Coras, Roland (Author) , Beckervordersandforth, Jan (Author) , Kim, Se Hoon (Author) , Rogerio, Fabio (Author) , Dimova, Petia S. (Author) , Niehusmann, Pitt (Author) , Unterberg, Andreas (Author) , Platten, Michael (Author) , Pfister, Stefan (Author) , Wick, Wolfgang (Author) , Herold-Mende, Christel (Author) , Deimling, Andreas von (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
2
Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course by Wefers, Annika K. (Author) , Stichel, Damian (Author) , Schrimpf, Daniel (Author) , Coras, Roland (Author) , Pages, Mélanie (Author) , Tauziède-Espariat, Arnault (Author) , Varlet, Pascale (Author) , Schwarz, Daniel (Author) , Söylemezoglu, Figen (Author) , Pohl, Ute (Author) , Pimentel, José (Author) , Meyer, Jochen (Author) , Hewer, Ekkehard (Author) , Japp, Anna (Author) , Joshi, Abhijit (Author) , Reuss, David (Author) , Reinhardt, Annekathrin (Author) , Sievers, Philipp (Author) , Casalini, Belén (Author) , Ebrahimi, Azadeh (Author) , Huang, Kristin (Author) , Kölsche, Christian (Author) , Pfister, Stefan (Author) , Sahm, Felix (Author) , Deimling, Andreas von (Author) , Jones, David T. W. (Author) , Blumcke, Ingmar (Author) , Capper, David (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
3
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay by Kobow, Katja (Author) , Jabari, Samir (Author) , Pieper, Tom (Author) , Kudernatsch, Manfred (Author) , Polster, Tilman (Author) , Woermann, Friedrich G. (Author) , Kalbhenn, Thilo (Author) , Hamer, Hajo (Author) , Rössler, Karl (Author) , Mühlebner, Angelika (Author) , Spliet, Wim G. M. (Author) , Feucht, Martha (Author) , Hou, Yanghao (Author) , Stichel, Damian (Author) , Korshunov, Andrey (Author) , Sahm, Felix (Author) , Coras, Roland (Author) , Blümcke, Ingmar (Author) , Deimling, Andreas von (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
4
Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype-phenotype analysis by Blümcke, Ingmar (Author) , Wefers, Annika K. (Author) , Capper, David (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
5
Histopathological findings in brain tissue obtained during epilepsy surgery by Blümcke, Ingmar (Author) , Diepgen, Thomas L. (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
6
Low-grade epilepsy-associated neuroepithelial tumours - the 2016 WHO classification by Blümcke, Ingmar (Author) , Aronica, Eleonora (Author) , Becker, Albert (Author) , Capper, David (Author) , Coras, Roland (Author) , Honavar, Mrinalini (Author) , Jacques, Thomas S. (Author) , Kobow, Katja (Author) , Miyata, Hajime (Author) , Mühlebner, Angelika (Author) , Pimentel, José (Author) , Söylemezoğlu, Figen (Author) , Thom, Maria (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
7
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases by Clemen, Christoph Stephan (Author) , Tangavelou, Karthikeyan (Author) , Strucksberg, Karl-Heinz (Author) , Just, Steffen (Author) , Manta, Linda (Author) , Regus-Leidig, Hanna (Author) , Stumpf, Maria (Author) , Reimann, Jens (Author) , Coras, Roland (Author) , Morgan, Reginald O. (Author) , Fernandez, Maria-Pilar (Author) , Hofmann, Andreas (Author) , Müller, Stefan (Author) , Schoser, Benedikt (Author) , Hanisch, Franz-Georg (Author) , Rottbauer, Wolfgang (Author) , Blümcke, Ingmar (Author) , von Hörsten, Stephan (Author) , Eichinger, Ludwig (Author) , Schröder, Rolf (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource
Search Tools:
Related Subjects
Animals
Blotting, Western
Brain development
Cell Line
Cells, Cultured
Chromosome 1
Copy number variation
Cortical malformation
DNA methylation analysis
Endoplasmic Reticulum
Genetic Predisposition to Disease
Humans
Huntingtin Protein
ID
Immunohistochemistry
Immunoprecipitation
Mass Spectrometry
Mice
Myositis, Inclusion Body
Nerve Tissue Proteins
Neurons
Nuclear Proteins
Proteins
Reverse Transcriptase Polymerase Chain Reaction
Seizures
Spastic Paraplegia, Hereditary
Wound Healing
Zebrafish
anaplastic ganglioglioma
brain tumour