person

Heidrun K. B.

Country
Germany
Department
Neurologie

Research Overview

Data & Insights

medical_services
Primary Speciality
Main therapeutic area

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Return Partnerships
Recurring site collaborations
0
Sites with multiple studies

Has run more than one trial at 0 of 68 partner sites.

Specializations

Cerebrovascular Disorders

Heidrun focuses on Acute Ischemic Stroke, High‑Risk Transient Ischemic Attack, and prevention of recurrent cerebrovascular events.

  • Acute Ischemic Stroke
  • High‑Risk Transient Ischemic Attack
  • Cardio‑embolic Stroke Management
  • Cerebral Small Vessel Disease
  • Stroke Prevention Strategies

Clinical work integrates vascular imaging and antithrombotic therapy optimization.

Epilepsy and Seizure Management

Research includes Convulsive Status Epilepticus in the elderly, focal epilepsy, and benzodiazepine‑resistant seizures.

  • Convulsive Status Epilepticus
  • Non‑convulsive Status Epilepticus
  • Focal Epilepsy
  • Primary Generalized Tonic‑Clonic Seizures
  • Benzodiazepine‑Resistant Seizures

Emphasis is placed on rapid pharmacologic intervention and EEG monitoring.

Neurodegenerative and Demyelinating Diseases

Heidrun investigates disease‑modifying strategies for Relapsing‑Remitting Multiple Sclerosis, Secondary Progressive Multiple Sclerosis, and neurodegeneration in Parkinson's Disease.

  • Relapsing‑Remitting Multiple Sclerosis
  • Secondary Progressive Multiple Sclerosis
  • Primary Progressive Multiple Sclerosis
  • Parkinson's Disease
  • Friedreich’s Ataxia

Studies address neuroprotective agents and immune modulation.

Neuro‑Oncology

Active involvement in pediatric and adult brain tumors such as Medulloblastoma and Ependymoma, with a focus on molecularly targeted therapies.

  • Medulloblastoma
  • Ependymoma
  • High‑Grade Glioma
  • Pediatric Brain Tumors
  • Neuroblastoma

Research integrates genomic profiling and innovative treatment protocols.

Neurogenetic and Rare Neurological Conditions

Work encompasses inherited disorders like Ataxia Telangiectasia, CACNA1A‑Related Disorders, and retinal dystrophies such as Leber Congenital Amaurosis.

  • Ataxia Telangiectasia
  • CACNA1A‑Related Disorders
  • Leber Congenital Amaurosis
  • Autosomal Dominant Optic Atrophy
  • Geographic Atrophy

Efforts combine genetic diagnostics with emerging gene‑therapy approaches.

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