Overview
Stephan Lobitz practices in Koblenz, Germany. Mr. Lobitz is highly rated in 6 conditions, according to our data. His top areas of expertise are Sickle Cell Disease, Hemoglobinopathy, Congenital Hemolytic Anemia, and Hemolytic Anemia.
His clinical research consists of co-authoring 28 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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
- AnemiaMr. Lobitz isDistinguished. Learn about Anemia.
- Congenital Hemolytic AnemiaMr. Lobitz isDistinguished. Learn about Congenital Hemolytic Anemia.
- HemoglobinopathyMr. Lobitz isDistinguished. Learn about Hemoglobinopathy.
- Hemolytic AnemiaMr. Lobitz isDistinguished. Learn about Hemolytic Anemia.
- Sickle Cell DiseaseMr. Lobitz isDistinguished. Learn about Sickle Cell Disease.
- Advanced
- Turcot SyndromeMr. Lobitz isAdvanced. Learn about Turcot Syndrome.
- Experienced
- Beta ThalassemiaMr. Lobitz isExperienced. Learn about Beta Thalassemia.
- Biotinidase DeficiencyMr. Lobitz isExperienced. Learn about Biotinidase Deficiency.
- Brain TumorMr. Lobitz isExperienced. Learn about Brain Tumor.
- Kearns-Sayre SyndromeMr. Lobitz isExperienced. Learn about Kearns-Sayre Syndrome.
- Lynch SyndromeMr. Lobitz isExperienced. Learn about Lynch Syndrome.
- Multiple Carboxylase DeficiencyMr. Lobitz isExperienced. Learn about Multiple Carboxylase Deficiency.