person

Marton K.

Country
Norway
Department
Department of Neurology

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 5 partner sites.

Specializations

Neurodegenerative Disorders

Investigator Marton König focuses on diseases characterized by progressive neuronal loss, including Alzheimer's Disease and Amyotrophic Lateral Sclerosis, as well as early cognitive decline such as Mild cognitive impairment.

  • Alzheimer's Disease
  • Amyotrophic Lateral Sclerosis
  • Mild cognitive impairment

Research aims to elucidate pathogenic mechanisms and identify disease‑modifying interventions.

Cerebrovascular and Stroke Medicine

Clinical work emphasizes acute and chronic vascular brain injury, notably Acute ischemic stroke, and associated cardiac rhythm disorders such as Atrial fibrillation after stress and broader atherosclerotic risk.

  • Acute ischemic stroke
  • Atrial fibrillation after stress
  • Atherosclerotic cardiovascular disease

Efforts target prevention, acute management, and long‑term vascular health.

Neuro‑immunology and Autoimmune Neurology

Investigator König engages in immune‑mediated neurological conditions, including Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyneuropathy, and antibody‑driven disorders such as Generalized Myasthenia Gravis.

  • Multiple Sclerosis
  • Chronic Inflammatory Demyelinating Polyneuropathy
  • Generalized Myasthenia Gravis

Studies explore immunopathology and therapeutic modulation of autoimmunity.

Neuro‑oncology

Research portfolio includes malignant brain tumors such as Glioblastoma, metastatic disease exemplified by Brain metastases from non‑small‑cell lung cancer, and pediatric solid tumours like Medulloblastoma.

  • Glioblastoma
  • Brain metastases from non‑small‑cell lung cancer
  • Medulloblastoma

Focus lies on molecular characterization and innovative treatment strategies.

Neuromuscular and Rare Genetic Neurology

Investigator König addresses hereditary neuromuscular disorders, including Duchenne Muscular Dystrophy, DNA‑repair syndromes such as Ataxia Telangiectasia, and motor neuron disease exemplified by Spinal Muscular Atrophy.

  • Duchenne Muscular Dystrophy
  • Ataxia Telangiectasia
  • Spinal Muscular Atrophy

Efforts aim to define disease pathways and assess emerging therapeutic approaches.

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