Overview
Khashti Joshi practices practicing medicine in Frankfurt Am Main, Germany.
Joshi is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Hyperlysinemia, Hyperprolinemia, Ornithine Translocase Deficiency, and Hereditary Xanthinuria.
They are actively involved in clinical research, co-authoring 40 peer reviewed articles.
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.
Frequently Asked Questions about Khashti B. Joshi
Is Khashti B. Joshi a top-rated expert for Hyperlysinemia?
MediFind is an objective health platform that identifies experts based on real-world data. Khashti B. Joshi is classified as an Advanced expert for Hyperlysinemia, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Khashti B. Joshi participate in research or clinical trials?
Yes. Khashti B. Joshi has published 40 articles and abstracts on conditions like Hyperlysinemia. You can view a list of Khashti B. Joshi's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- HyperlysinemiaJoshi isAdvanced. Learn about Hyperlysinemia.
- HyperprolinemiaJoshi isAdvanced. Learn about Hyperprolinemia.
- Experienced
- Hereditary XanthinuriaJoshi isExperienced. Learn about Hereditary Xanthinuria.
- HypermethioninemiaJoshi isExperienced. Learn about Hypermethioninemia.
- Methicillin-Resistant Staphylococcus Aureus (MRSA)
- Ornithine Translocase Deficiency
- Urea Cycle Disorders (UCD)Joshi isExperienced. Learn about Urea Cycle Disorders (UCD).