Overview
Sacha Ferdinandusse practices practicing medicine in Amsterdam, Netherlands.
Ms. Ferdinandusse is highly rated in 26 conditions, according to our data. Her clinical expertise encompasses Zellweger Syndrome, Primary Carnitine Deficiency, Protein Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
She is actively involved in clinical research, co-authoring 137 peer reviewed articles.
Gender
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.
Frequently Asked Questions about Sacha Ferdinandusse
Is Sacha Ferdinandusse a top-rated expert for Zellweger Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Sacha Ferdinandusse is classified as an Elite expert for Zellweger Syndrome, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Sacha Ferdinandusse participate in research or clinical trials?
Yes. Sacha Ferdinandusse has published 137 articles and abstracts on conditions like Zellweger Syndrome. You can view a list of Sacha Ferdinandusse's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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.
- 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.
- Protein DeficiencyMs. Ferdinandusse isDistinguished. Learn about Protein Deficiency.
- Refsum DiseaseMs. Ferdinandusse isDistinguished. Learn about Refsum Disease.
- RhabdomyolysisMs. Ferdinandusse isDistinguished. Learn about Rhabdomyolysis.
- Sjogren-Larsson SyndromeMs. Ferdinandusse isDistinguished. Learn about Sjogren-Larsson Syndrome.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) DeficiencyMs. Ferdinandusse isDistinguished. Learn about Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) 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.
- GalactosemiaMs. Ferdinandusse isAdvanced. Learn about Galactosemia.
- Glutaric Acidemia Type 2Ms. Ferdinandusse isAdvanced. Learn about Glutaric Acidemia Type 2.
- HyperlysinemiaMs. Ferdinandusse isAdvanced. Learn about Hyperlysinemia.
- Leigh SyndromeMs. Ferdinandusse isAdvanced. Learn about Leigh Syndrome.
- Malonyl-CoA Decarboxylase DeficiencyMs. Ferdinandusse isAdvanced. Learn about Malonyl-CoA Decarboxylase Deficiency.
- MicrognathiaMs. Ferdinandusse isAdvanced. Learn about Micrognathia.
- Newborn Low Blood SugarMs. Ferdinandusse isAdvanced. Learn about Newborn Low Blood Sugar.
- Pyruvate Dehydrogenase DeficiencyMs. Ferdinandusse isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- X-Linked Chondrodysplasia Punctata 2Ms. Ferdinandusse isAdvanced. Learn about X-Linked Chondrodysplasia Punctata 2.
- Yunis-Varon SyndromeMs. Ferdinandusse isAdvanced. Learn about Yunis-Varon Syndrome.
- Experienced
- Acromicric DysplasiaMs. Ferdinandusse isExperienced. Learn about Acromicric Dysplasia.
- Adrenal Insufficiency PediatricMs. Ferdinandusse isExperienced. Learn about Adrenal Insufficiency Pediatric.
- 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.
- CACH SyndromeMs. Ferdinandusse isExperienced. Learn about CACH Syndrome.
- CardiomyopathyMs. Ferdinandusse isExperienced. Learn about Cardiomyopathy.
- ChondrodystrophyMs. Ferdinandusse isExperienced. Learn about Chondrodystrophy.
- Cleidocranial DysplasiaMs. Ferdinandusse isExperienced. Learn about Cleidocranial Dysplasia.
- Clouston SyndromeMs. Ferdinandusse isExperienced. Learn about Clouston Syndrome.
- Congenital ContracturesMs. Ferdinandusse isExperienced. Learn about Congenital Contractures.
- Dilated Cardiomyopathy (DCM)Ms. Ferdinandusse isExperienced. Learn about Dilated Cardiomyopathy (DCM).
- Drug Induced DyskinesiaMs. Ferdinandusse isExperienced. Learn about Drug Induced Dyskinesia.
- Ectodermal DysplasiasMs. Ferdinandusse isExperienced. Learn about Ectodermal Dysplasias.
- Gyrate Atrophy of the Choroid and RetinaMs. Ferdinandusse isExperienced. Learn about Gyrate Atrophy of the Choroid and Retina.
- Hearing LossMs. Ferdinandusse isExperienced. Learn about Hearing Loss.
- HemiplegiaMs. Ferdinandusse isExperienced. Learn about Hemiplegia.
- Hereditary Spastic ParaparesisMs. Ferdinandusse isExperienced. Learn about Hereditary Spastic Paraparesis.
- Lactic AcidosisMs. Ferdinandusse isExperienced. Learn about Lactic Acidosis.
- Lamellar IchthyosisMs. Ferdinandusse isExperienced. Learn about Lamellar Ichthyosis.
- Low Blood SugarMs. Ferdinandusse isExperienced. Learn about Low Blood Sugar.
- MalnutritionMs. Ferdinandusse isExperienced. Learn about Malnutrition.
- Metabolic AcidosisMs. Ferdinandusse isExperienced. Learn about Metabolic Acidosis.
- Miller SyndromeMs. Ferdinandusse isExperienced. Learn about Miller Syndrome.
- Movement DisordersMs. Ferdinandusse isExperienced. Learn about Movement Disorders.
- Nonbullous Congenital Ichthyosiform ErythrodermaMs. Ferdinandusse isExperienced. Learn about Nonbullous Congenital Ichthyosiform Erythroderma.
- Pontocerebellar HypoplasiaMs. Ferdinandusse isExperienced. Learn about Pontocerebellar Hypoplasia.
- Propionic AcidemiaMs. Ferdinandusse isExperienced. Learn about Propionic Acidemia.
- Pyruvate Decarboxylase DeficiencyMs. Ferdinandusse isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Retinopathy Pigmentary Mental RetardationMs. Ferdinandusse isExperienced. Learn about Retinopathy Pigmentary Mental Retardation.
- Schwartz-Jampel SyndromeMs. Ferdinandusse isExperienced. Learn about Schwartz-Jampel Syndrome.
- Sensorimotor PolyneuropathyMs. Ferdinandusse isExperienced. Learn about Sensorimotor Polyneuropathy.
- Spastic Paraplegia Type 2Ms. Ferdinandusse isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Ms. Ferdinandusse isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityMs. Ferdinandusse isExperienced. Learn about Spasticity.
- X-Linked Spondyloepiphyseal Dysplasia TardaMs. Ferdinandusse isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.