Overview
Matthias Christen practices in Bern, Switzerland. Mr. Christen is rated as a Distinguished expert by MediFind in the treatment of L-2-Hydroxyglutaric Aciduria. His top areas of expertise are L-2-Hydroxyglutaric Aciduria, Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects, Acute Cerebellar Ataxia, and Piebaldism.
His clinical research consists of co-authoring 47 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of L-2-Hydroxyglutaric Aciduria.
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
- L-2-Hydroxyglutaric AciduriaMr. Christen isDistinguished. Learn about L-2-Hydroxyglutaric Aciduria.
- Advanced
- Acute Cerebellar AtaxiaMr. Christen isAdvanced. Learn about Acute Cerebellar Ataxia.
- Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects
- PiebaldismMr. Christen isAdvanced. Learn about Piebaldism.
- Experienced
- AlbinismMr. Christen isExperienced. Learn about Albinism.
- AnhidrosisMr. Christen isExperienced. Learn about Anhidrosis.
- Batten DiseaseMr. Christen isExperienced. Learn about Batten Disease.
- CLN1 DiseaseMr. Christen isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMr. Christen isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMr. Christen isExperienced. Learn about CLN3 Disease.