Overview
Pushpa Joshi practices practicing medicine in Halle, Germany.
Joshi is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Carnitine Palmitoyltransferase 1 Deficiency, Carnitine Palmitoyltransferase 2 Deficiency, Glycogen Storage Disease Type 5, and Myoglobinuria Recurrent.
They are actively involved in clinical research, co-authoring 17 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 Pushpa R. Joshi
Is Pushpa R. Joshi a top-rated expert for Carnitine Palmitoyltransferase 1 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Pushpa R. Joshi is classified as an Advanced expert for Carnitine Palmitoyltransferase 1 Deficiency, 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 Pushpa R. Joshi participate in research or clinical trials?
Yes. Pushpa R. Joshi has published 17 articles and abstracts on conditions like Carnitine Palmitoyltransferase 1 Deficiency. You can view a list of Pushpa R. 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
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Glycogen Storage Disease Type 5
- Experienced
- Acute PainJoshi isExperienced. Learn about Acute Pain.
- Adenosine Monophosphate Deaminase Deficiency
- Congenital Fiber-Type Disproportion
- Congenital Myasthenic Syndrome
- Myoglobinuria RecurrentJoshi isExperienced. Learn about Myoglobinuria Recurrent.
- Progressive External Ophthalmoplegia
- RhabdomyolysisJoshi isExperienced. Learn about Rhabdomyolysis.
- Tubular Aggregate MyopathyJoshi isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular MyopathyJoshi isExperienced. Learn about X-Linked Myotubular Myopathy.