person

Terry G.J. D.

Country
The Netherlands
Department
Beatrix Childrens' Hospital, Dept. of Metabolic Diseases

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 7 partner sites.

Specializations

Pediatric Metabolic Disorders

Focus on inherited metabolic conditions affecting children, including disorders of carbohydrate metabolism, lipid metabolism, and amino acid metabolism.

  • Glycogen storage disease type I
  • Medium-chain acyl‑CoA dehydrogenase deficiency
  • Phenylketonuria
  • Urea cycle disorders
  • Organic acidemia

Therapeutic strategies emphasize enzyme replacement, dietary modulation, and gene therapy approaches.

Hematologic Malignancies

Investigation of blood‑borne cancers, especially lymphoid and myeloid neoplasms across age groups.

  • Acute myeloid leukemia
  • Diffuse large B‑cell lymphoma
  • Chronic lymphocytic leukemia
  • Mantle cell lymphoma
  • Myelodysplastic syndromes

Targeted agents and immunotherapies are evaluated to improve remission durability.

Autoimmune and Inflammatory Diseases

Clinical research on systemic autoimmune disorders and organ‑specific inflammation.

  • Systemic lupus erythematosus
  • Rheumatoid arthritis
  • Inflammatory bowel disease
  • Atopic dermatitis
  • Vasculitis

Biologic modulators of cytokine pathways are a central focus.

Cardiovascular and Renal Syndromes

Studies addressing heart failure, atherosclerotic disease, and progressive kidney pathology.

  • Heart failure with preserved ejection fraction
  • Atrial fibrillation
  • Transthyretin amyloid cardiomyopathy
  • Chronic kidney disease
  • Polycystic kidney disease

Interventions aim to modify hemodynamic stress and renal fibrosis.

Rare Genetic and Neurological Conditions

Exploration of uncommon hereditary disorders impacting neurological function and multisystem health.

  • Hereditary angioedema
  • Multiple system atrophy
  • Primary sclerosing cholangitis
  • Ehlers‑Danlos syndrome
  • Spinal muscular atrophy

Precision medicine tools such as CRISPR‑based editing are being assessed.

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