Overview
Hugo Rocha practices in Porto, Portugal. Mr. Rocha is rated as an Experienced expert by MediFind in the treatment of Primary Carnitine Deficiency. His top areas of expertise are Glutaric Acidemia Type 2, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Rhabdomyolysis, and Primary Lateral Sclerosis.
His clinical research consists of co-authoring 32 peer reviewed articles. 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.
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
- Glutaric Acidemia Type 2Mr. Rocha isDistinguished. Learn about Glutaric Acidemia Type 2.
- Advanced
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Congenital HypothyroidismMr. Rocha isExperienced. Learn about Congenital Hypothyroidism.
- Gestational DiabetesMr. Rocha isExperienced. Learn about Gestational Diabetes.
- Mucopolysaccharidoses (MPS)Mr. Rocha isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Neonatal HypothyroidismMr. Rocha isExperienced. Learn about Neonatal Hypothyroidism.