Overview
Samarth Kulshrestha practices in New Delhi, India. Mr. Kulshrestha is rated as an Advanced expert by MediFind in the treatment of Atelosteogenesis Type 2. His top areas of expertise are Atelosteogenesis Type 2, Craniofacial-Deafness-Hand Syndrome, Familial Hypercholesterolemia, and Deafness Craniofacial Syndrome.
His clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Atelosteogenesis Type 2.
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
- Atelosteogenesis Type 2Mr. Kulshrestha isAdvanced. Learn about Atelosteogenesis Type 2.
- Craniofacial-Deafness-Hand SyndromeMr. Kulshrestha isAdvanced. Learn about Craniofacial-Deafness-Hand Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeMr. Kulshrestha isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Arthrogryposis Multiplex CongenitaMr. Kulshrestha isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Brachydactyly Mononen TypeMr. Kulshrestha isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyMr. Kulshrestha isExperienced. Learn about Chondrodystrophy.
- Congenital ContracturesMr. Kulshrestha isExperienced. Learn about Congenital Contractures.
- Cortical DysplasiaMr. Kulshrestha isExperienced. Learn about Cortical Dysplasia.