Overview
Sacha Ferdinandusse practices in Amsterdam, Netherlands. Ms. Ferdinandusse is rated as a Distinguished expert by MediFind in the treatment of Refsum Disease. Her top areas of expertise are Zellweger Syndrome, Primary Carnitine Deficiency, Protein Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
Her clinical research consists of co-authoring 140 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 8 articles in the study of Refsum Disease.
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
- Elite
- Primary Carnitine DeficiencyMs. Ferdinandusse isElite. Learn about Primary Carnitine Deficiency.
- Zellweger SyndromeMs. Ferdinandusse isElite. Learn about Zellweger Syndrome.
- Distinguished
- Classic GalactosemiaMs. Ferdinandusse isDistinguished. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMs. Ferdinandusse isDistinguished. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Ferdinandusse isDistinguished. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Ferdinandusse isDistinguished. Learn about Galactosemia.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase DeficiencyMs. Ferdinandusse isDistinguished. Learn about Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.
- Mitochondrial Trifunctional Protein DeficiencyMs. Ferdinandusse isDistinguished. Learn about Mitochondrial Trifunctional Protein Deficiency.
- Advanced
- Addison's DiseaseMs. Ferdinandusse isAdvanced. Learn about Addison's Disease.
- Adrenoleukodystrophy (ALD)Ms. Ferdinandusse isAdvanced. Learn about Adrenoleukodystrophy (ALD).
- Barth SyndromeMs. Ferdinandusse isAdvanced. Learn about Barth Syndrome.
- Chondrodysplasia Punctata SyndromeMs. Ferdinandusse isAdvanced. Learn about Chondrodysplasia Punctata Syndrome.
- Glutaric Acidemia Type 2Ms. Ferdinandusse isAdvanced. Learn about Glutaric Acidemia Type 2.
- HyperlysinemiaMs. Ferdinandusse isAdvanced. Learn about Hyperlysinemia.
- Experienced
- Acromicric DysplasiaMs. Ferdinandusse isExperienced. Learn about Acromicric Dysplasia.
- Acute Cerebellar AtaxiaMs. Ferdinandusse isExperienced. Learn about Acute Cerebellar Ataxia.
- Alternating Hemiplegia of ChildhoodMs. Ferdinandusse isExperienced. Learn about Alternating Hemiplegia of Childhood.
- Aplasia Cutis CongenitaMs. Ferdinandusse isExperienced. Learn about Aplasia Cutis Congenita.
- Arthrogryposis Multiplex CongenitaMs. Ferdinandusse isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Brachydactyly Mononen TypeMs. Ferdinandusse isExperienced. Learn about Brachydactyly Mononen Type.