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Person

Martha Feucht

Ärztin

Name	Martha Feucht
Time	1991- (Wirkungsdaten)
Place	Österreich
Academic degree	Prof. Dr.
Profession	Ärztin (characteristic profession)
Related	Universitäts-Klinik für Kinder- und Jugendheilkunde (Wien) Epilepsie (Thema)
Record type	Person
GND-Identifier	1251625215
Record ID	1251625215
Involved in show all Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years Implementation of a 7T Epilepsy Task Force consensus imaging protocol for routine presurgical epilepsy work-up: effect on diagnostic yield and lesion delineation Author Correction: Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment How can we optimize the long-term outcome in children with intracranial cavernous malformations? A single-center experience of 61 cases Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal period DNA methylation-based classification of malformations of cortical development in the human brain Distinct DNA Methylation Patterns of Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex Fieberkrämpfe – Diagnostik und Behandlung Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA) Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): new findings from the TOSCA TAND research project TSC2 pathogenic variants are predictive of severe clinical manifestations in TSC infants: results of the EPISTOP study TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy Epilepsy surgery in infants : Safety issues and developmental outcome Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment TuberOus SClerosis registry to increase disease Awareness (TOSCA) – baseline data on 2093 patients Efficacy and safety of Everolimus in children with TSC - associated epilepsy – Pilot data from an open single-center prospective study Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis complex (TSC): evidence from layer-specific marker expression The Role of mTOR Inhibitors in the Treatment of Patients with Tuberous Sclerosis Complex: Evidence-based and Expert Opinions Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis complex (TSC): evidence from layer-specific marker expression Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies TOSCA – first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex Erfahrungen mit Generika bei Epilepsiepatienten : Ergebnisse einer Internet-basierten Befragung in Deutschland, Österreich und der Schweiz *

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Katalog der Deutschen Nationalbibliothek

Martha Feucht

Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years

Implementation of a 7T Epilepsy Task Force consensus imaging protocol for routine presurgical epilepsy work-up: effect on diagnostic yield and lesion delineation

Author Correction: Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment

How can we optimize the long-term outcome in children with intracranial cavernous malformations? A single-center experience of 61 cases

Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal period

DNA methylation-based classification of malformations of cortical development in the human brain

Distinct DNA Methylation Patterns of Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex

Fieberkrämpfe – Diagnostik und Behandlung

Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA)

Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay

Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): new findings from the TOSCA TAND research project

TSC2 pathogenic variants are predictive of severe clinical manifestations in TSC infants: results of the EPISTOP study

TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study

Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy

Epilepsy surgery in infants : Safety issues and developmental outcome

Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment

TuberOus SClerosis registry to increase disease Awareness (TOSCA) – baseline data on 2093 patients

Efficacy and safety of Everolimus in children with TSC - associated epilepsy – Pilot data from an open single-center prospective study

Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis complex (TSC): evidence from layer-specific marker expression

The Role of mTOR Inhibitors in the Treatment of Patients with Tuberous Sclerosis Complex: Evidence-based and Expert Opinions

Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis complex (TSC): evidence from layer-specific marker expression

Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies

TOSCA – first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex

Erfahrungen mit Generika bei Epilepsiepatienten : Ergebnisse einer Internet-basierten Befragung in Deutschland, Österreich und der Schweiz *