Overview
Consuelo Giner-Pedron practices in Nino Jesus, Spain. Ms. Giner-Pedron is rated as an Advanced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. Her top areas of expertise are Hereditary Fructose Intolerance, Homocystinuria due to MTHFR Deficiency, Homocystinuria, Phosphomannoisomerase Deficiency, and Gastrostomy.
Her clinical research consists of co-authoring 49 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Homocystinuria due to MTHFR Deficiency.
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. Giner-Pedron isDistinguished. Learn about Hereditary Fructose Intolerance.
- Advanced
- GastrostomyMs. Giner-Pedron isAdvanced. Learn about Gastrostomy.
- HomocystinuriaMs. Giner-Pedron isAdvanced. Learn about Homocystinuria.
- Homocystinuria due to MTHFR DeficiencyMs. Giner-Pedron isAdvanced. Learn about Homocystinuria due to MTHFR Deficiency.
- Inborn Renal AminoaciduriaMs. Giner-Pedron isAdvanced. Learn about Inborn Renal Aminoaciduria.
- Maternal HyperphenylalaninemiaMs. Giner-Pedron isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Phosphomannoisomerase DeficiencyMs. Giner-Pedron isAdvanced. Learn about Phosphomannoisomerase Deficiency.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyMs. Giner-Pedron isExperienced. Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
- Absence SeizureMs. Giner-Pedron isExperienced. Learn about Absence Seizure.
- Childhood VolvulusMs. Giner-Pedron isExperienced. Learn about Childhood Volvulus.
- CitrullinemiaMs. Giner-Pedron isExperienced. Learn about Citrullinemia.
- CystinuriaMs. Giner-Pedron isExperienced. Learn about Cystinuria.
- EpilepsyMs. Giner-Pedron isExperienced. Learn about Epilepsy.