Overview
Helena Valta practices in Helsinki, Finland. Ms. Valta is rated as a Distinguished expert by MediFind in the treatment of Chondrodystrophy. Her top areas of expertise are Cartilage-Hair Hypoplasia, Chondrodystrophy, X-Linked Spondyloepiphyseal Dysplasia Tarda, and Schwartz-Jampel Syndrome.
Her clinical research consists of co-authoring 39 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 10 articles in the study of Chondrodystrophy.
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
- Cartilage-Hair HypoplasiaMs. Valta isDistinguished. Learn about Cartilage-Hair Hypoplasia.
- ChondrodystrophyMs. Valta isDistinguished. Learn about Chondrodystrophy.
- Schwartz-Jampel SyndromeMs. Valta isDistinguished. Learn about Schwartz-Jampel Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia Tarda
- Advanced
- Brachydactyly Mononen TypeMs. Valta isAdvanced. Learn about Brachydactyly Mononen Type.
- Familial Hypocalciuric Hypercalcemia Type 1
- HypercalcemiaMs. Valta isAdvanced. Learn about Hypercalcemia.
- Milk-Alkali SyndromeMs. Valta isAdvanced. Learn about Milk-Alkali Syndrome.
- Osteogenesis ImperfectaMs. Valta isAdvanced. Learn about Osteogenesis Imperfecta.
- Experienced
- Acromesomelic DysplasiaMs. Valta isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED)
- Autoimmune Polyglandular Syndrome Type 2