Overview
Maria Gozalbo-Rubio practices practicing medicine in Maastricht, Netherlands.
Ms. Gozalbo-Rubio is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses Classic Galactosemia, Galactosemia, Galactokinase Deficiency, and Galactose Epimerase Deficiency.
She is actively involved in clinical research, co-authoring 83 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 Maria E. Gozalbo-Rubio
Is Maria E. Gozalbo-Rubio a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Maria E. Gozalbo-Rubio 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 Maria E. Gozalbo-Rubio participate in research or clinical trials?
Yes. Maria E. Gozalbo-Rubio has published 83 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Maria E. Gozalbo-Rubio'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. Gozalbo-Rubio isElite. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMs. Gozalbo-Rubio isElite. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Gozalbo-Rubio isElite. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Gozalbo-Rubio isElite. Learn about Galactosemia.
- Advanced
- Hereditary Fructose IntoleranceMs. Gozalbo-Rubio isAdvanced. Learn about Hereditary Fructose Intolerance.
- Mucolipidosis Type 4Ms. Gozalbo-Rubio isAdvanced. Learn about Mucolipidosis Type 4.
- Phenylketonuria (PKU)Ms. Gozalbo-Rubio isAdvanced. Learn about Phenylketonuria (PKU).
- Tyrosinemia Type 1Ms. Gozalbo-Rubio isAdvanced. Learn about Tyrosinemia Type 1.
- Zellweger SyndromeMs. Gozalbo-Rubio isAdvanced. Learn about Zellweger Syndrome.
- Experienced
- CataractMs. Gozalbo-Rubio isExperienced. Learn about Cataract.
- Glutaric Acidemia Type 2Ms. Gozalbo-Rubio isExperienced. Learn about Glutaric Acidemia Type 2.
- InfertilityMs. Gozalbo-Rubio isExperienced. Learn about Infertility.
- Maple Syrup Urine DiseaseMs. Gozalbo-Rubio isExperienced. Learn about Maple Syrup Urine Disease.
- Medium-Chain Acyl-CoA Dehydrogenase DeficiencyMs. Gozalbo-Rubio isExperienced. Learn about Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
- Methylmalonic AcidemiaMs. Gozalbo-Rubio isExperienced. Learn about Methylmalonic Acidemia.
- Movement DisordersMs. Gozalbo-Rubio isExperienced. Learn about Movement Disorders.
- MPI-CDGMs. Gozalbo-Rubio isExperienced. Learn about MPI-CDG.
- Mucolipidosis 3Ms. Gozalbo-Rubio isExperienced. Learn about Mucolipidosis 3.
- Newborn Low Blood SugarMs. Gozalbo-Rubio isExperienced. Learn about Newborn Low Blood Sugar.
- Premature Ovarian FailureMs. Gozalbo-Rubio isExperienced. Learn about Premature Ovarian Failure.
- Propionic AcidemiaMs. Gozalbo-Rubio isExperienced. Learn about Propionic Acidemia.
- SialidosisMs. Gozalbo-Rubio isExperienced. Learn about Sialidosis.
- Von Gierke DiseaseMs. Gozalbo-Rubio isExperienced. Learn about Von Gierke Disease.