Overview
Patricia Correcher practices practicing medicine in Valencia, Spain.
Ms. Correcher is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Hereditary Fructose Intolerance, Maple Syrup Urine Disease, Phosphomannoisomerase Deficiency, and Galactosemia.
She is actively involved in clinical research, co-authoring 16 peer reviewed articles.
Gender
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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 Patricia Correcher
Is Patricia Correcher a top-rated expert for Hereditary Fructose Intolerance?
MediFind is an objective health platform that identifies experts based on real-world data. Patricia Correcher 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 Patricia Correcher participate in research or clinical trials?
Yes. Patricia Correcher has published 16 articles and abstracts on conditions like Hereditary Fructose Intolerance. You can view a list of Patricia Correcher'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. Correcher isDistinguished. Learn about Hereditary Fructose Intolerance.
- Advanced
- Maple Syrup Urine DiseaseMs. Correcher isAdvanced. Learn about Maple Syrup Urine Disease.
- Phosphomannoisomerase DeficiencyMs. Correcher isAdvanced. Learn about Phosphomannoisomerase Deficiency.
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Correcher isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Classic GalactosemiaMs. Correcher isExperienced. Learn about Classic Galactosemia.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Correcher isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Folate DeficiencyMs. Correcher isExperienced. Learn about Folate Deficiency.
- Galactokinase DeficiencyMs. Correcher isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Correcher isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Correcher isExperienced. Learn about Galactosemia.
- Inborn Amino Acid Metabolism DisorderMs. Correcher isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Niemann-Pick DiseaseMs. Correcher isExperienced. Learn about Niemann-Pick Disease.
- Phenylketonuria (PKU)Ms. Correcher isExperienced. Learn about Phenylketonuria (PKU).
- Urea Cycle Disorders (UCD)Ms. Correcher isExperienced. Learn about Urea Cycle Disorders (UCD).