Overview
Lodewijk Ijlst practices in Amsterdam, Netherlands. Ijlst is rated as an Experienced expert by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. Their top areas of expertise are Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Protein Deficiency, Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), and Rhabdomyolysis.
Their clinical research consists of co-authoring 47 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 1 article in the study of Carbamoyl Phosphate Synthetase 1 Deficiency.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Advanced
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Mitochondrial Trifunctional Protein Deficiency
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Protein DeficiencyIjlst isAdvanced. Learn about Protein Deficiency.
- Experienced
- Barth SyndromeIjlst isExperienced. Learn about Barth Syndrome.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CardiomyopathyIjlst isExperienced. Learn about Cardiomyopathy.
- Hereditary Spastic Paraparesis
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- N-Acetylglutamate Synthase Deficiency