Overview
Maria Couce practices practicing medicine in Santiago De Compostela, Spain.
Couce is highly rated in 33 conditions, according to our data. Their clinical expertise encompasses Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Hereditary Fructose Intolerance, and Mucopolysaccharidoses (MPS).
They are actively involved in clinical research, co-authoring 164 peer reviewed articles.
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 L. Couce
Is Maria L. Couce a top-rated expert for Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)?
MediFind is an objective health platform that identifies experts based on real-world data. Maria L. Couce is classified as an Distinguished expert for Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B), 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 L. Couce participate in research or clinical trials?
Yes. Maria L. Couce has published 164 articles and abstracts on conditions like Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B). You can view a list of Maria L. Couce'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
- Classic GalactosemiaCouce isDistinguished. Learn about Classic Galactosemia.
- Galactokinase DeficiencyCouce isDistinguished. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyCouce isDistinguished. Learn about Galactose Epimerase Deficiency.
- GalactosemiaCouce isDistinguished. Learn about Galactosemia.
- Hereditary Fructose IntoleranceCouce isDistinguished. Learn about Hereditary Fructose Intolerance.
- Homocystinuria due to MTHFR Deficiency
- Inborn Amino Acid Metabolism Disorder
- Mucopolysaccharidoses (MPS)Couce isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Phosphomannoisomerase DeficiencyCouce isDistinguished. Learn about Phosphomannoisomerase Deficiency.
- Advanced
- ALG6-CDGCouce isAdvanced. Learn about ALG6-CDG.
- Argininosuccinic Aciduria
- Biotinidase DeficiencyCouce isAdvanced. Learn about Biotinidase Deficiency.
- Brachydactyly Mononen Type
- DPAGT1-CDGCouce isAdvanced. Learn about DPAGT1-CDG.
- GalactosialidosisCouce isAdvanced. Learn about Galactosialidosis.
- HomocystinuriaCouce isAdvanced. Learn about Homocystinuria.
- HypermethioninemiaCouce isAdvanced. Learn about Hypermethioninemia.
- Hypophosphatasia (HPP)Couce isAdvanced. Learn about Hypophosphatasia (HPP).
- Isovaleric AcidemiaCouce isAdvanced. Learn about Isovaleric Acidemia.
- Lactose IntoleranceCouce isAdvanced. Learn about Lactose Intolerance.
- Maple Syrup Urine Disease
- Maternal Hyperphenylalaninemia
- Methylmalonic AcidemiaCouce isAdvanced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A)
- Multiple Carboxylase Deficiency
- Phenylketonuria (PKU)Couce isAdvanced. Learn about Phenylketonuria (PKU).
- Premature InfantCouce isAdvanced. Learn about Premature Infant.
- SRD5A3-CDGCouce isAdvanced. Learn about SRD5A3-CDG.
- Urea Cycle Disorders (UCD)
- Experienced
- AchondroplasiaCouce isExperienced. Learn about Achondroplasia.
- ADULT SyndromeCouce isExperienced. Learn about ADULT Syndrome.
- ALG1-CDGCouce isExperienced. Learn about ALG1-CDG.
- Batten DiseaseCouce isExperienced. Learn about Batten Disease.
- Bronchopulmonary DysplasiaCouce isExperienced. Learn about Bronchopulmonary Dysplasia.
- CardiomyopathyCouce isExperienced. Learn about Cardiomyopathy.
- CataractCouce isExperienced. Learn about Cataract.
- Childhood Hypophosphatasia (HPP)
- Childhood PancreatitisCouce isExperienced. Learn about Childhood Pancreatitis.
- Cholesteryl Ester Storage Disease
- ChondrodystrophyCouce isExperienced. Learn about Chondrodystrophy.
- CLN1 DiseaseCouce isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseCouce isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseCouce isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseCouce isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseCouce isExperienced. Learn about CLN5 Disease.
- Congenital CataractCouce isExperienced. Learn about Congenital Cataract.
- Disseminated Intravascular Coagulation
- Drug Induced DyskinesiaCouce isExperienced. Learn about Drug Induced Dyskinesia.
- Exocrine Pancreatic Insufficiency
- Fabry DiseaseCouce isExperienced. Learn about Fabry Disease.
- Folate DeficiencyCouce isExperienced. Learn about Folate Deficiency.
- Glycine EncephalopathyCouce isExperienced. Learn about Glycine Encephalopathy.
- Infant HyperglycemiaCouce isExperienced. Learn about Infant Hyperglycemia.
- Lactic AcidosisCouce isExperienced. Learn about Lactic Acidosis.
- Low Blood SugarCouce isExperienced. Learn about Low Blood Sugar.
- Lysosomal Acid Lipase Deficiency
- MacroglossiaCouce isExperienced. Learn about Macroglossia.
- MalabsorptionCouce isExperienced. Learn about Malabsorption.
- Mitochondrial Complex 1 Deficiency
- MPI-CDGCouce isExperienced. Learn about MPI-CDG.
- Mucolipidosis 3Couce isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Couce isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple Sulfatase DeficiencyCouce isExperienced. Learn about Multiple Sulfatase Deficiency.
- NecrosisCouce isExperienced. Learn about Necrosis.
- Necrotizing EnterocolitisCouce isExperienced. Learn about Necrotizing Enterocolitis.
- Newborn Low Blood SugarCouce isExperienced. Learn about Newborn Low Blood Sugar.
- ObesityCouce isExperienced. Learn about Obesity.
- Obesity in ChildrenCouce isExperienced. Learn about Obesity in Children.
- OsteopeniaCouce isExperienced. Learn about Osteopenia.
- OsteoporosisCouce isExperienced. Learn about Osteoporosis.
- Patent Ductus ArteriosusCouce isExperienced. Learn about Patent Ductus Arteriosus.
- PGM1-CDGCouce isExperienced. Learn about PGM1-CDG.
- PMM2-Congenital Disorder of Glycosylation
- Pompe DiseaseCouce isExperienced. Learn about Pompe Disease.
- Propionic AcidemiaCouce isExperienced. Learn about Propionic Acidemia.
- RFT1-CDGCouce isExperienced. Learn about RFT1-CDG.
- Schwartz-Jampel SyndromeCouce isExperienced. Learn about Schwartz-Jampel Syndrome.
- Sengers SyndromeCouce isExperienced. Learn about Sengers Syndrome.
- SepsisCouce isExperienced. Learn about Sepsis.
- Septo-Optic DysplasiaCouce isExperienced. Learn about Septo-Optic Dysplasia.
- SialidosisCouce isExperienced. Learn about Sialidosis.
- SpasticityCouce isExperienced. Learn about Spasticity.
- Tyrosinemia Type 1Couce isExperienced. Learn about Tyrosinemia Type 1.
- Von Gierke DiseaseCouce isExperienced. Learn about Von Gierke Disease.
- Wolman DiseaseCouce isExperienced. Learn about Wolman Disease.
- X-Linked Spondyloepiphyseal Dysplasia Tarda