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Christian Thomas

Arzt

Name	Christian Thomas
Place	Münster (Westf) (Wirkungsort) Deutschland
Academic degree	Dr.
Profession	Arzt (characteristic profession)
Further information	Assistenzarzt, Klinik für Allgemeine Neurologie, Universitätsklinikum Münster
Record type	Person
GND-Identifier	1133590608
Record ID	1133590608
Involved in show all Cell-mediated cytotoxicity within CSF and brain parenchyma in spinal muscular atrophy unaltered by nusinersen treatment Nanopore sequencing from formalin-fixed paraffin-embedded specimens for copy-number profiling and methylation-based CNS tumor classification ATRT–SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance TERT promoter mutation and chromosome 6 loss define a high-risk subtype of ependymoma evolving from posterior fossa subependymoma Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1 Pediatric atypical choroid plexus papilloma reconsidered: increased mitotic activity is prognostic only in older children

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Christian Thomas

Cell-mediated cytotoxicity within CSF and brain parenchyma in spinal muscular atrophy unaltered by nusinersen treatment

Nanopore sequencing from formalin-fixed paraffin-embedded specimens for copy-number profiling and methylation-based CNS tumor classification

ATRT–SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance

TERT promoter mutation and chromosome 6 loss define a high-risk subtype of ependymoma evolving from posterior fossa subependymoma

Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults

Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1

Pediatric atypical choroid plexus papilloma reconsidered: increased mitotic activity is prognostic only in older children