Overview
Irm Borgmeyer-Hermans practices practicing medicine in Hamburg, Germany.
Borgmeyer-Hermans is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Glucose Transporter Deficiency, Spondyloepiphyseal Dysplasia, Membranous Nephropathy, and Spondyloepiphyseal Dysplasia Congenita.
They are actively involved in clinical research, co-authoring 47 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 Irm Borgmeyer-Hermans
Is Irm Borgmeyer-Hermans a top-rated expert for Glucose Transporter Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Irm Borgmeyer-Hermans is classified as an Advanced expert for Glucose Transporter 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 Irm Borgmeyer-Hermans participate in research or clinical trials?
Yes. Irm Borgmeyer-Hermans has published 47 articles and abstracts on conditions like Glucose Transporter Deficiency. You can view a list of Irm Borgmeyer-Hermans'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
- Glucose Transporter DeficiencyBorgmeyer-Hermans isAdvanced. Learn about Glucose Transporter Deficiency.
- Experienced
- Brachydactyly Mononen TypeBorgmeyer-Hermans isExperienced. Learn about Brachydactyly Mononen Type.
- Caffey DiseaseBorgmeyer-Hermans isExperienced. Learn about Caffey Disease.
- Cerebellar HypoplasiaBorgmeyer-Hermans isExperienced. Learn about Cerebellar Hypoplasia.
- ChondrodystrophyBorgmeyer-Hermans isExperienced. Learn about Chondrodystrophy.
- GlomerulonephritisBorgmeyer-Hermans isExperienced. Learn about Glomerulonephritis.
- Hajdu-Cheney SyndromeBorgmeyer-Hermans isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hereditary Sensory and Autonomic Neuropathy Type 2Borgmeyer-Hermans isExperienced. Learn about Hereditary Sensory and Autonomic Neuropathy Type 2.
- High CholesterolBorgmeyer-Hermans isExperienced. Learn about High Cholesterol.
- Membranous NephropathyBorgmeyer-Hermans isExperienced. Learn about Membranous Nephropathy.
- Memory LossBorgmeyer-Hermans isExperienced. Learn about Memory Loss.
- Mucolipidosis 3Borgmeyer-Hermans isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Borgmeyer-Hermans isExperienced. Learn about Mucolipidosis Type 4.
- Osteogenesis ImperfectaBorgmeyer-Hermans isExperienced. Learn about Osteogenesis Imperfecta.
- Schwartz-Jampel SyndromeBorgmeyer-Hermans isExperienced. Learn about Schwartz-Jampel Syndrome.
- SialidosisBorgmeyer-Hermans isExperienced. Learn about Sialidosis.
- Spondyloepiphyseal DysplasiaBorgmeyer-Hermans isExperienced. Learn about Spondyloepiphyseal Dysplasia.
- Spondyloepiphyseal Dysplasia CongenitaBorgmeyer-Hermans isExperienced. Learn about Spondyloepiphyseal Dysplasia Congenita.
- X-Linked Creatine DeficiencyBorgmeyer-Hermans isExperienced. Learn about X-Linked Creatine Deficiency.
- X-Linked Spondyloepiphyseal Dysplasia TardaBorgmeyer-Hermans isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.