Overview
Marcela Amieva-Vela practices practicing medicine in Mexico, Mexico.
Ms. Amieva-Vela is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Isovaleric Acidemia, Propionic Acidemia, and Inborn Amino Acid Metabolism Disorder.
She is actively involved in clinical research, co-authoring 62 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 Marcela Amieva-Vela
Is Marcela Amieva-Vela a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Marcela Amieva-Vela is classified as an Advanced expert for Phenylketonuria (PKU), 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 Marcela Amieva-Vela participate in research or clinical trials?
Yes. Marcela Amieva-Vela has published 62 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Marcela Amieva-Vela'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
- Advanced
- Glucose-Galactose Malabsorption DeficiencyMs. Amieva-Vela isAdvanced. Learn about Glucose-Galactose Malabsorption Deficiency.
- Inborn Amino Acid Metabolism DisorderMs. Amieva-Vela isAdvanced. Learn about Inborn Amino Acid Metabolism Disorder.
- Isovaleric AcidemiaMs. Amieva-Vela isAdvanced. Learn about Isovaleric Acidemia.
- Methylmalonic AcidemiaMs. Amieva-Vela isAdvanced. Learn about Methylmalonic Acidemia.
- Phenylketonuria (PKU)Ms. Amieva-Vela isAdvanced. Learn about Phenylketonuria (PKU).
- Propionic AcidemiaMs. Amieva-Vela isAdvanced. Learn about Propionic Acidemia.
- Experienced
- Abdominal Obesity Metabolic SyndromeMs. Amieva-Vela isExperienced. Learn about Abdominal Obesity Metabolic Syndrome.
- AnemiaMs. Amieva-Vela isExperienced. Learn about Anemia.
- Arginase DeficiencyMs. Amieva-Vela isExperienced. Learn about Arginase Deficiency.
- Bilirubin EncephalopathyMs. Amieva-Vela isExperienced. Learn about Bilirubin Encephalopathy.
- Congenital Hemolytic AnemiaMs. Amieva-Vela isExperienced. Learn about Congenital Hemolytic Anemia.
- Congenital HyperinsulinismMs. Amieva-Vela isExperienced. Learn about Congenital Hyperinsulinism.
- Congenital HypothyroidismMs. Amieva-Vela isExperienced. Learn about Congenital Hypothyroidism.
- CystinosisMs. Amieva-Vela isExperienced. Learn about Cystinosis.
- DehydrationMs. Amieva-Vela isExperienced. Learn about Dehydration.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Amieva-Vela isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Familial HypertriglyceridemiaMs. Amieva-Vela isExperienced. Learn about Familial Hypertriglyceridemia.
- Glucose-6-Phosphate Dehydrogenase DeficiencyMs. Amieva-Vela isExperienced. Learn about Glucose-6-Phosphate Dehydrogenase Deficiency.
- Hairy Cell Leukemia (HCL)Ms. Amieva-Vela isExperienced. Learn about Hairy Cell Leukemia (HCL).
- Hemolytic AnemiaMs. Amieva-Vela isExperienced. Learn about Hemolytic Anemia.
- Hemolytic Disease of the NewbornMs. Amieva-Vela isExperienced. Learn about Hemolytic Disease of the Newborn.
- HypothyroidismMs. Amieva-Vela isExperienced. Learn about Hypothyroidism.
- JaundiceMs. Amieva-Vela isExperienced. Learn about Jaundice.
- Maple Syrup Urine DiseaseMs. Amieva-Vela isExperienced. Learn about Maple Syrup Urine Disease.
- Metabolic AcidosisMs. Amieva-Vela isExperienced. Learn about Metabolic Acidosis.
- Metabolic SyndromeMs. Amieva-Vela isExperienced. Learn about Metabolic Syndrome.
- Newborn JaundiceMs. Amieva-Vela isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarMs. Amieva-Vela isExperienced. Learn about Newborn Low Blood Sugar.
- ObesityMs. Amieva-Vela isExperienced. Learn about Obesity.
- Obesity in ChildrenMs. Amieva-Vela isExperienced. Learn about Obesity in Children.
- Ornithine Transcarbamylase DeficiencyMs. Amieva-Vela isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Primary Tubular Proximal AcidosisMs. Amieva-Vela isExperienced. Learn about Primary Tubular Proximal Acidosis.
- Proximal Renal Tubular AcidosisMs. Amieva-Vela isExperienced. Learn about Proximal Renal Tubular Acidosis.
- Renal Tubular AcidosisMs. Amieva-Vela isExperienced. Learn about Renal Tubular Acidosis.
- Spinocerebellar Ataxia Type 7Ms. Amieva-Vela isExperienced. Learn about Spinocerebellar Ataxia Type 7.
- Transient Familial HyperbilirubinemiaMs. Amieva-Vela isExperienced. Learn about Transient Familial Hyperbilirubinemia.
- Tyrosinemia Type 1Ms. Amieva-Vela isExperienced. Learn about Tyrosinemia Type 1.
- Urea Cycle Disorders (UCD)Ms. Amieva-Vela isExperienced. Learn about Urea Cycle Disorders (UCD).