Overview
Karlien Coene practices practicing medicine in Veldhoven, Netherlands.
Coene is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency, Hyperprolinemia, Phenylketonuria (PKU), and Hereditary Xanthinuria.
They are actively involved in clinical research, co-authoring 35 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 Karlien M. Coene
Is Karlien M. Coene a top-rated expert for Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Karlien M. Coene is classified as an Advanced expert for Delta-1-Pyrroline-5-Carboxylate Dehydrogenase 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 Karlien M. Coene participate in research or clinical trials?
Yes. Karlien M. Coene has published 35 articles and abstracts on conditions like Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency. You can view a list of Karlien M. Coene'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
- Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency
- HyperprolinemiaCoene isAdvanced. Learn about Hyperprolinemia.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Ataxia-TelangiectasiaCoene isExperienced. Learn about Ataxia-Telangiectasia.
- DysarthriaCoene isExperienced. Learn about Dysarthria.
- EpilepsyCoene isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenCoene isExperienced. Learn about Epilepsy in Children.
- Generalized Tonic-Clonic Seizure
- Glutaric Acidemia Type 2Coene isExperienced. Learn about Glutaric Acidemia Type 2.
- Hereditary XanthinuriaCoene isExperienced. Learn about Hereditary Xanthinuria.
- Inborn Amino Acid Metabolism Disorder
- Monoamine Oxidase A Deficiency
- Phenylketonuria (PKU)Coene isExperienced. Learn about Phenylketonuria (PKU).
- Succinic Semialdehyde Dehydrogenase Deficiency
- TelangiectasiaCoene isExperienced. Learn about Telangiectasia.
- X-Linked Creatine DeficiencyCoene isExperienced. Learn about X-Linked Creatine Deficiency.