Experienced in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency

Wulf Roschinger

Munich, BY, DE 
Experienced in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
Munich, BY, DE 
OverviewLocationsClinical Research

Overview

Wulf Roschinger practices in Munich, Germany. Mr. Roschinger is rated as an Experienced expert by MediFind in the treatment of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. His top areas of expertise are Primary Lateral Sclerosis, Spinal Muscular Atrophy (SMA), Vitamin B12 Deficiency Anemia, and Propionic Acidemia.

His clinical research consists of co-authoring 27 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.

Gender
Male

Locations

Munich, BY 81671, Germany

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.

27 Total Publications

A Modular Genetic Approach to Newborn Screening from Spinal Muscular Atrophy to Sickle Cell Disease-Results from Six Years of Genetic Newborn Screening.
A Modular Genetic Approach to Newborn Screening from Spinal Muscular Atrophy to Sickle Cell Disease-Results from Six Years of Genetic Newborn Screening.
Journal: Genes
Published: October 07, 2024

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.

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