Overview
Annet Bosch practices practicing medicine in Amsterdam, Netherlands.
Ms. Bosch is highly rated in 18 conditions, according to our data. Her clinical expertise encompasses Classic Galactosemia, Riboflavin Transporter Deficiency Neuronopathy, Galactosemia, and Galactokinase Deficiency.
She is actively involved in clinical research, co-authoring 117 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 Annet M. Bosch
Is Annet M. Bosch a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Annet M. Bosch is classified as an Elite expert for Classic Galactosemia, 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 Annet M. Bosch participate in research or clinical trials?
Yes. Annet M. Bosch has published 117 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Annet M. Bosch'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
- Classic GalactosemiaMs. Bosch isElite. Learn about Classic Galactosemia.
- Riboflavin Transporter Deficiency Neuronopathy
- Distinguished
- Galactokinase DeficiencyMs. Bosch isDistinguished. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Bosch isDistinguished. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Bosch isDistinguished. Learn about Galactosemia.
- Phenylketonuria (PKU)Ms. Bosch isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Congenital HypothyroidismMs. Bosch isAdvanced. Learn about Congenital Hypothyroidism.
- Glutaric Acidemia Type 2Ms. Bosch isAdvanced. Learn about Glutaric Acidemia Type 2.
- Holocarboxylase Synthetase Deficiency
- HypothyroidismMs. Bosch isAdvanced. Learn about Hypothyroidism.
- Maple Syrup Urine DiseaseMs. Bosch isAdvanced. Learn about Maple Syrup Urine Disease.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Methylmalonic AcidemiaMs. Bosch isAdvanced. Learn about Methylmalonic Acidemia.
- Neonatal HypothyroidismMs. Bosch isAdvanced. Learn about Neonatal Hypothyroidism.
- Primary Lateral SclerosisMs. Bosch isAdvanced. Learn about Primary Lateral Sclerosis.
- Propionic AcidemiaMs. Bosch isAdvanced. Learn about Propionic Acidemia.
- Tyrosinemia Type 1Ms. Bosch isAdvanced. Learn about Tyrosinemia Type 1.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- CataractMs. Bosch isExperienced. Learn about Cataract.
- Cholesteryl Ester Storage DiseaseMs. Bosch isExperienced. Learn about Cholesteryl Ester Storage Disease.
- Congenital Adrenal Hyperplasia (CAH)Ms. Bosch isExperienced. Learn about Congenital Adrenal Hyperplasia (CAH).
- Developmental Dysphasia FamilialMs. Bosch isExperienced. Learn about Developmental Dysphasia Familial.
- Glutaric Acidemia Type 1Ms. Bosch isExperienced. Learn about Glutaric Acidemia Type 1.
- Hearing LossMs. Bosch isExperienced. Learn about Hearing Loss.
- HypotoniaMs. Bosch isExperienced. Learn about Hypotonia.
- InfertilityMs. Bosch isExperienced. Learn about Infertility.
- IntersexMs. Bosch isExperienced. Learn about Intersex.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Lysosomal Acid Lipase DeficiencyMs. Bosch isExperienced. Learn about Lysosomal Acid Lipase Deficiency.
- MalnutritionMs. Bosch isExperienced. Learn about Malnutrition.
- Maternal HyperphenylalaninemiaMs. Bosch isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Mitochondrial Trifunctional Protein Deficiency
- Movement DisordersMs. Bosch isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Newborn Low Blood SugarMs. Bosch isExperienced. Learn about Newborn Low Blood Sugar.
- Niemann-Pick DiseaseMs. Bosch isExperienced. Learn about Niemann-Pick Disease.
- Olivopontocerebellar AtrophyMs. Bosch isExperienced. Learn about Olivopontocerebellar Atrophy.
- Palatopharyngeal IncompetenceMs. Bosch isExperienced. Learn about Palatopharyngeal Incompetence.
- Protein DeficiencyMs. Bosch isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisMs. Bosch isExperienced. Learn about Rhabdomyolysis.
- Spinocerebellar AtaxiaMs. Bosch isExperienced. Learn about Spinocerebellar Ataxia.
- Trophoblastic Tumor Placental SiteMs. Bosch isExperienced. Learn about Trophoblastic Tumor Placental Site.
- Urea Cycle Disorders (UCD)Ms. Bosch isExperienced. Learn about Urea Cycle Disorders (UCD).
- Vitamin B12 DeficiencyMs. Bosch isExperienced. Learn about Vitamin B12 Deficiency.
- Vitamin B12 Deficiency AnemiaMs. Bosch isExperienced. Learn about Vitamin B12 Deficiency Anemia.
- Wolman DiseaseMs. Bosch isExperienced. Learn about Wolman Disease.