Overview
Deniz Kanber practices in Essen, Germany. Kanber is rated as an Experienced expert by MediFind in the treatment of Prader-Willi Syndrome. Their top areas of expertise are Retinoblastoma, Chromosome 13q Deletion, Angelman Syndrome, and Chromosome 6 Uniparental Disomy.
Their clinical research consists of co-authoring 25 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 2 articles in the study of Prader-Willi Syndrome.
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
- Angelman SyndromeKanber isAdvanced. Learn about Angelman Syndrome.
- Chromosome 13q DeletionKanber isAdvanced. Learn about Chromosome 13q Deletion.
- Chromosome 6 Uniparental Disomy
- RetinoblastomaKanber isAdvanced. Learn about Retinoblastoma.
- Experienced
- Cornelia De Lange SyndromeKanber isExperienced. Learn about Cornelia De Lange Syndrome.
- Gliomatosis CerebriKanber isExperienced. Learn about Gliomatosis Cerebri.
- HypotoniaKanber isExperienced. Learn about Hypotonia.
- MosaicismKanber isExperienced. Learn about Mosaicism.
- Prader-Willi SyndromeKanber isExperienced. Learn about Prader-Willi Syndrome.