Overview
Esmeralda Martins-Gomes practices in Santo Antonio De Felheiros, Portugal. Ms. Martins-Gomes is highly rated in 10 conditions, according to our data. Her top areas of expertise are Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), RFT1-CDG, Phenylketonuria (PKU), and Tyrosinemia Type 3.
Her clinical research consists of co-authoring 54 peer reviewed articles and participating in 3 clinical trials. 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.
3 Clinical Trials
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
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)Ms. Martins-Gomes isDistinguished. Learn about Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome).
- RFT1-CDGMs. Martins-Gomes isDistinguished. Learn about RFT1-CDG.
- Advanced
- DPAGT1-CDGMs. Martins-Gomes isAdvanced. Learn about DPAGT1-CDG.
- Glutaric Acidemia Type 2Ms. Martins-Gomes isAdvanced. Learn about Glutaric Acidemia Type 2.
- Mucopolysaccharidoses (MPS)Ms. Martins-Gomes isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Phenylketonuria (PKU)Ms. Martins-Gomes isAdvanced. Learn about Phenylketonuria (PKU).
- Phosphomannoisomerase DeficiencyMs. Martins-Gomes isAdvanced. Learn about Phosphomannoisomerase Deficiency.
- PMM2-Congenital Disorder of GlycosylationMs. Martins-Gomes isAdvanced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Experienced
- ALG1-CDGMs. Martins-Gomes isExperienced. Learn about ALG1-CDG.
- Arginase DeficiencyMs. Martins-Gomes isExperienced. Learn about Arginase Deficiency.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1Ms. Martins-Gomes isExperienced. Learn about Camptodactyly Syndrome Guadalajara Type 1.
- Camptodactyly Syndrome Guadalajara Type 2Ms. Martins-Gomes isExperienced. Learn about Camptodactyly Syndrome Guadalajara Type 2.
- Camptodactyly TaurinuriaMs. Martins-Gomes isExperienced. Learn about Camptodactyly Taurinuria.