Overview
Patrick Verloo practices practicing medicine in Gent, Belgium.
His clinical expertise encompasses Ornithine Translocase Deficiency, Bilateral Perisylvian Polymicrogyria, Polymicrogyria, and Periventricular Heterotopia.
He is actively involved in clinical research, co-authoring 25 peer reviewed articles and participating in 1 clinical trial.
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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.
1 Clinical Trials
Frequently Asked Questions about Patrick Verloo
Is Patrick Verloo a top-rated expert for Ornithine Translocase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Patrick Verloo is classified as an Experienced expert for Ornithine Translocase 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 Patrick Verloo participate in research or clinical trials?
Yes. Patrick Verloo has published 25 articles and abstracts on conditions like Ornithine Translocase Deficiency. You can view a list of Patrick Verloo'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
- Experienced
- Acromicric DysplasiaMr. Verloo isExperienced. Learn about Acromicric Dysplasia.
- Aicardi-Goutieres SyndromeMr. Verloo isExperienced. Learn about Aicardi-Goutieres Syndrome.
- Apolipoprotein C2 DeficiencyMr. Verloo isExperienced. Learn about Apolipoprotein C2 Deficiency.
- Bilateral Perisylvian PolymicrogyriaMr. Verloo isExperienced. Learn about Bilateral Perisylvian Polymicrogyria.
- Classic GalactosemiaMr. Verloo isExperienced. Learn about Classic Galactosemia.
- Drug Induced DyskinesiaMr. Verloo isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaMr. Verloo isExperienced. Learn about Dysarthria.
- Epilepsy in ChildrenMr. Verloo isExperienced. Learn about Epilepsy in Children.
- Familial Lipoprotein Lipase DeficiencyMr. Verloo isExperienced. Learn about Familial Lipoprotein Lipase Deficiency.
- Galactokinase DeficiencyMr. Verloo isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Verloo isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Verloo isExperienced. Learn about Galactosemia.
- HypospadiasMr. Verloo isExperienced. Learn about Hypospadias.
- HypotoniaMr. Verloo isExperienced. Learn about Hypotonia.
- JaundiceMr. Verloo isExperienced. Learn about Jaundice.
- Mucolipidosis 3Mr. Verloo isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Mr. Verloo isExperienced. Learn about Mucolipidosis Type 4.
- Newborn JaundiceMr. Verloo isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarMr. Verloo isExperienced. Learn about Newborn Low Blood Sugar.
- Ornithine Translocase DeficiencyMr. Verloo isExperienced. Learn about Ornithine Translocase Deficiency.
- Periventricular HeterotopiaMr. Verloo isExperienced. Learn about Periventricular Heterotopia.
- PolymicrogyriaMr. Verloo isExperienced. Learn about Polymicrogyria.
- Primary HyperoxaluriaMr. Verloo isExperienced. Learn about Primary Hyperoxaluria.
- Primary Hyperoxaluria Type 1Mr. Verloo isExperienced. Learn about Primary Hyperoxaluria Type 1.
- RhabdomyolysisMr. Verloo isExperienced. Learn about Rhabdomyolysis.
- SeizuresMr. Verloo isExperienced. Learn about Seizures.
- SplenomegalyMr. Verloo isExperienced. Learn about Splenomegaly.
- SyndactylyMr. Verloo isExperienced. Learn about Syndactyly.
- ThrombocytopeniaMr. Verloo isExperienced. Learn about Thrombocytopenia.
- Transient Familial HyperbilirubinemiaMr. Verloo isExperienced. Learn about Transient Familial Hyperbilirubinemia.
- Urea Cycle Disorders (UCD)Mr. Verloo isExperienced. Learn about Urea Cycle Disorders (UCD).