Overview
Petr Chrastina practices in Prague, Czech Republic. Mr. Chrastina is rated as an Advanced expert by MediFind in the treatment of Homocystinuria due to MTHFR Deficiency. His top areas of expertise are Carnitine Palmitoyltransferase 1 Deficiency, Homocystinuria due to MTHFR Deficiency, Carnitine-Acylcarnitine Translocase Deficiency, and Glycogen Storage Disease Type 7.
His clinical research consists of co-authoring 13 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 Homocystinuria due to MTHFR Deficiency.
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
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine-Acylcarnitine Translocase Deficiency
- Homocystinuria due to MTHFR DeficiencyMr. Chrastina isAdvanced. Learn about Homocystinuria due to MTHFR Deficiency.
- Experienced
- Adrenoleukodystrophy (ALD)Mr. Chrastina isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Glutaric Acidemia Type 1Mr. Chrastina isExperienced. Learn about Glutaric Acidemia Type 1.
- Glycogen Storage Disease Type 7Mr. Chrastina isExperienced. Learn about Glycogen Storage Disease Type 7.
- HomocystinuriaMr. Chrastina isExperienced. Learn about Homocystinuria.
- Isovaleric AcidemiaMr. Chrastina isExperienced. Learn about Isovaleric Acidemia.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency