Overview
Silvia Calzada-Chumillas practices practicing medicine in Madrid, Spain.
Ms. Calzada-Chumillas is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses Hereditary Fructose Intolerance, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Inborn Renal Aminoaciduria, and Phosphomannoisomerase Deficiency.
She is actively involved in clinical research, co-authoring 10 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 Silvia Calzada-Chumillas
Is Silvia Calzada-Chumillas a top-rated expert for Hereditary Fructose Intolerance?
MediFind is an objective health platform that identifies experts based on real-world data. Silvia Calzada-Chumillas is classified as an Distinguished expert for Hereditary Fructose Intolerance, 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 Silvia Calzada-Chumillas participate in research or clinical trials?
Yes. Silvia Calzada-Chumillas has published 10 articles and abstracts on conditions like Hereditary Fructose Intolerance. You can view a list of Silvia Calzada-Chumillas'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
- Distinguished
- Hereditary Fructose IntoleranceMs. Calzada-Chumillas isDistinguished. Learn about Hereditary Fructose Intolerance.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyMs. Calzada-Chumillas isAdvanced. Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
- Inborn Renal AminoaciduriaMs. Calzada-Chumillas isAdvanced. Learn about Inborn Renal Aminoaciduria.
- Phosphomannoisomerase DeficiencyMs. Calzada-Chumillas isAdvanced. Learn about Phosphomannoisomerase Deficiency.
- Experienced
- CitrullinemiaMs. Calzada-Chumillas isExperienced. Learn about Citrullinemia.
- CystinuriaMs. Calzada-Chumillas isExperienced. Learn about Cystinuria.
- Folate DeficiencyMs. Calzada-Chumillas isExperienced. Learn about Folate Deficiency.
- Glutaric Acidemia Type 2Ms. Calzada-Chumillas isExperienced. Learn about Glutaric Acidemia Type 2.
- HomocystinuriaMs. Calzada-Chumillas isExperienced. Learn about Homocystinuria.
- HypermethioninemiaMs. Calzada-Chumillas isExperienced. Learn about Hypermethioninemia.
- Inborn Amino Acid Metabolism DisorderMs. Calzada-Chumillas isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseMs. Calzada-Chumillas isExperienced. Learn about Maple Syrup Urine Disease.
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyMs. Calzada-Chumillas isExperienced. Learn about Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
- Methylmalonic AcidemiaMs. Calzada-Chumillas isExperienced. Learn about Methylmalonic Acidemia.
- Ornithine Transcarbamylase DeficiencyMs. Calzada-Chumillas isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Propionic AcidemiaMs. Calzada-Chumillas isExperienced. Learn about Propionic Acidemia.
- Urea Cycle Disorders (UCD)Ms. Calzada-Chumillas isExperienced. Learn about Urea Cycle Disorders (UCD).
- Vitamin B12 DeficiencyMs. Calzada-Chumillas isExperienced. Learn about Vitamin B12 Deficiency.
- Vitamin B12 Deficiency AnemiaMs. Calzada-Chumillas isExperienced. Learn about Vitamin B12 Deficiency Anemia.