Overview
Juan Paz-Lopez practices in Bilbao, Spain. Mr. Paz-Lopez is highly rated in 4 conditions, according to our data. His top areas of expertise are Chiari Malformation Type 1, Chiari Malformation, Chiari Malformation Type 2, Glucose Transporter Deficiency, and Posterior Fossa Decompression.
His clinical research consists of co-authoring 30 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
- Advanced
- Chiari MalformationMr. Paz-Lopez isAdvanced. Learn about Chiari Malformation.
- Chiari Malformation Type 1Mr. Paz-Lopez isAdvanced. Learn about Chiari Malformation Type 1.
- Chiari Malformation Type 2Mr. Paz-Lopez isAdvanced. Learn about Chiari Malformation Type 2.
- Glucose Transporter DeficiencyMr. Paz-Lopez isAdvanced. Learn about Glucose Transporter Deficiency.
- Experienced
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Becker Muscular DystrophyMr. Paz-Lopez isExperienced. Learn about Becker Muscular Dystrophy.
- Cramp-Fasciculation SyndromeMr. Paz-Lopez isExperienced. Learn about Cramp-Fasciculation Syndrome.
- Duchenne Muscular DystrophyMr. Paz-Lopez isExperienced. Learn about Duchenne Muscular Dystrophy.
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Multiple Sulfatase DeficiencyMr. Paz-Lopez isExperienced. Learn about Multiple Sulfatase Deficiency.