Overview
Alexej Knaus practices in Bonn, Germany. Knaus is rated as a Distinguished expert by MediFind in the treatment of Glucose Phosphate Isomerase Deficiency. Their top areas of expertise are Glucose Phosphate Isomerase Deficiency, Fryns Syndrome, Multiple Synostoses Syndrome 1, and Brachydactyly Type B.
Their clinical research consists of co-authoring 44 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 8 articles in the study of Glucose Phosphate Isomerase Deficiency.
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
- Fryns SyndromeKnaus isDistinguished. Learn about Fryns Syndrome.
- Glucose Phosphate Isomerase Deficiency
- Multiple Synostoses Syndrome 1Knaus isDistinguished. Learn about Multiple Synostoses Syndrome 1.
- Advanced
- Brachydactyly Type BKnaus isAdvanced. Learn about Brachydactyly Type B.
- Craniofacial-Deafness-Hand Syndrome
- Generalized Tonic-Clonic Seizure
- HypotoniaKnaus isAdvanced. Learn about Hypotonia.
- Experienced
- Absence SeizureKnaus isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly Syndrome
- Acromesomelic DysplasiaKnaus isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type