Overview
Marta Ivars practices in Barcelona, Spain. Ms. Ivars is rated as an Advanced expert by MediFind in the treatment of Familial Multiple Nevi Flammei. Her top areas of expertise are Stork Bite, Familial Multiple Nevi Flammei, Congenital Hypotrichosis Milia, and Megalencephaly-Capillary Malformation Syndrome.
Her clinical research consists of co-authoring 35 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 4 articles in the study of Familial Multiple Nevi Flammei.
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.
1 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
- Advanced
- Congenital Hypotrichosis MiliaMs. Ivars isAdvanced. Learn about Congenital Hypotrichosis Milia.
- Cutis Marmorata Telangiectatica Congenita
- Familial Multiple Nevi FlammeiMs. Ivars isAdvanced. Learn about Familial Multiple Nevi Flammei.
- HemangiomaMs. Ivars isAdvanced. Learn about Hemangioma.
- Megalencephaly-Capillary Malformation Syndrome
- Phacomatosis PigmentokeratoticaMs. Ivars isAdvanced. Learn about Phacomatosis Pigmentokeratotica.
- Experienced
- Acanthosis NigricansMs. Ivars isExperienced. Learn about Acanthosis Nigricans.
- AchondrogenesisMs. Ivars isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMs. Ivars isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type