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Person
Person

Person

Thomas Bast (1965-)

Arzt

Name

Thomas Bast

Time

1965- (Date of birth and death)

Place

Dillingen/Saar (Geburtsort)
Heidelberg (1992-1998 und 1999-2009) (Wirkungsort)
Deutschland

Gender

männlich

Academic degree

Habil. (Universität Heidelberg) (2007)
Dr. med. (Universität Heidelberg) (1995)

Profession

Arzt (characteristic profession)

Variant

Th. Bast

Related

Epilepsiezentrum Kork (2009-)
Universitätsklinikum Heidelberg (bis 2009)
Epilepsie (Thema)

Further information

Arbeitsschwerpunkt: Epilepsiediagnostik; Arzt; seit 01.07.2009 Chefarzt der Epilepsieklinik für Kinder und Jugendliche; 16.04.2015 Umhabilitation an die Albert-Ludwigs-Universität Freiburg

Record type

Person

GND-Identifier

131607685

Record ID

131607685

Involved in

show all

Caregivers’ experiences and expectations regarding seizure monitoring – a survey-based study

Off-label-Use von anfallssuppressiver und immunsuppressiver Medikation bei Epilepsien : Definition, Anwendungsfelder und praktisches Vorgehen

Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome : A prospective multicenter study in Germany

Ketogene Diäten bei Kindern mit tuberöse Sklerose Komplex

Kortikosteroide und adrenocorticotropes Hormon bei Epilepsien der frühen Kindheit jenseits des Säuglingsalters : : Bericht über einen systematischen Review mit Metaanalyse = Corticosteroids and adrenocorticotropic hormone in early childhood epilepsy beyond infancy : Report on a systematic review with meta-analysis

Sleep disturbances and health-related quality of life in children with epilepsy: A caregiver survey

Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly Patients

Epilepsy monitoring devices in children and adolescents. English version : The perspective of families

Kortikosteroide und adrenocorticotropes Hormon bei Epilepsien der frühen Kindheit jenseits des Säuglingsalters : Bericht über einen systematischen Review mit Metaanalyse

Technical note: preliminary surgical experience with a new implantable epicranial stimulation device for chronic focal cortex stimulation in drug-resistant epilepsy

Clinical characteristics and quality of life with Dravet syndrome: results of the German cohort of the Dravet syndrome caregiver survey (DISCUSS) = Klinische Charakteristika und Lebensqualität beim Dravet-Syndrom: Ergebnisse der deutschen Kohorte des „Dravet syndrome caregiver survey“ (DISCUSS)

Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: a prospective multicenter study in Germany

Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): a systematic review and meta-analysis

Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): a systematic review and meta‐analysis

Medikamenten-Pocket Epilepsie : Pharmakotherapie bei Kindern und Jugendlichen

Medikamenten-Pocket Epilepsie : Pharmakotherapie bei Kindern und Jugendlichen

Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders

Technical note: preliminary surgical experience with a new implantable epicranial stimulation device for chronic focal cortex stimulation in drug-resistant epilepsy

Epilepsieüberwachungsgeräte bei Kindern und Jugendlichen : Die Sicht der Familien

Akuter epileptischer Anfall – Handlungspläne für Laien (HEAL) und Therapeuten (HEAT)

Akuter epileptischer Anfall – Handlungspläne für Laien (HEAL) und Therapeuten (HEAT) = Acute epileptic seizure—Seizure action plans for laypersons (HEAL) and therapists (HEAT)

Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany

Valproate associated brain volume‐loss in pediatric epilepsy – a case series

Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome

“Within a minute” detection of focal cortical dysplasia

Efficacy, tolerability, and retention of antiseizure medications in PRRT2-associated infantile epilepsy

Klinische Charakteristika und Lebensqualität beim Dravet-Syndrom: Ergebnisse der deutschen Kohorte des „Dravet syndrome caregiver survey“ (DISCUSS) = Clinical characteristics and quality of life with Dravet syndrome: results of the German cohort of the Dravet syndrome caregiver survey (DISCUSS)

“Within a minute” detection of focal cortical dysplasia

Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients’ Perspectives

Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study

Consensus statements on the information to deliver after a febrile seizure

SCN1A-assoziierte Epilepsie mit foudroyantem Verlauf: Nicht immer muss die Langzeitprognose schlecht sein!

Epilepsy surgery: late seizure recurrence after initial complete seizure freedom

Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder

Refining genotypes and phenotypes in KCNA2-related neurological disorders

SUDEP („sudden unexpected death in epilepsy“) bei Kindern und Jugendlichen – Zahlen, Daten, Fakten

Could the 2017 ILAE and the four-dimensional epilepsy classifications be merged to a new "Integrated Epilepsy Classification"?

Focal epilepsy in SCN1A‐mutation carrying patients: is there a role for epilepsy surgery?

The phenotypic spectrum of PRRT2-associated paroxysmal neurologic disorders in childhood

The phenotypic spectrum of PRRT2-associated paroxysmal neurologic disorders in childhood

The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood

Drug Development for Rare Paediatric Epilepsies: Current State and Future Directions

Klinische Charakteristika, Ressourcenverbrauch, Lebensqualität und Versorgungssituation beim Dravet-Syndrom in Deutschland

Cannabidiol Interacts Significantly with Everolimus—Report of a Patient with Tuberous Sclerosis Complex

Congenital Lymphatic Malformation and Aortic Aneurysm in a Patient with TSC2 Mutation

A multicenter, matched case‐control analysis comparing burden‐of‐illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany

Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers : : a prospective, multicenter study from Germany

Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers : a prospective, multicenter study from Germany

Seizure management and prescription patterns of anticonvulsants in Dravet syndrome: A multicenter cohort study from Germany and review of literature

Structural brain anomalies in patients with FOX1 syndrome and in Foxg1+/− mice

Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/− mice

Aufgaben und Struktur moderner Epilepsiezentren in Deutschland

FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Erratum: Age-Dependency of Location of Epileptic Foci in “Continuous Spike-and-Waves during Sleep”: A Parallel to the Posterior-Anterior Trajectory of Slow Wave Activity

Age-Dependency of Location of Epileptic Foci in “Continuous Spike-and-Waves during Sleep”: A Parallel to the Posterior-Anterior Trajectory of Slow Wave Activity

Erster epileptischer Anfall und Epilepsien im Erwachsenenalter

Erster epileptischer Anfall und Epilepsien im Erwachsenenalter

Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences

Efficacy and Tolerability of Methylprednisolone Pulse Therapy in Childhood Epilepsies Other Than Infantile Spasms
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