Overview
Patricia Correcher practices in Valencia, Spain. Ms. Correcher is highly rated in 3 conditions, according to our data. Her top areas of expertise are Hereditary Fructose Intolerance, Maple Syrup Urine Disease, Phosphomannoisomerase Deficiency, and Galactosemia.
Her clinical research consists of co-authoring 13 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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
- 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.