Overview
Laila Wareth practices practicing medicine in Abu Dhabi, United Arab Emirates.
Her clinical expertise encompasses Biotinidase Deficiency, Multiple Carboxylase Deficiency, Metabolic Syndrome, and Galactosemia.
She is actively involved in clinical research, co-authoring 11 peer reviewed articles.
Gender
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 Laila A. Wareth
Is Laila A. Wareth a top-rated expert for Biotinidase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Laila A. Wareth is classified as an Experienced expert for Biotinidase 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 Laila A. Wareth participate in research or clinical trials?
Yes. Laila A. Wareth has published 11 articles and abstracts on conditions like Biotinidase Deficiency. You can view a list of Laila A. Wareth'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
- Alpha ThalassemiaMs. Wareth isExperienced. Learn about Alpha Thalassemia.
- Biotinidase DeficiencyMs. Wareth isExperienced. Learn about Biotinidase Deficiency.
- Classic GalactosemiaMs. Wareth isExperienced. Learn about Classic Galactosemia.
- Congenital HypothyroidismMs. Wareth isExperienced. Learn about Congenital Hypothyroidism.
- Galactokinase DeficiencyMs. Wareth isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Wareth isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Wareth isExperienced. Learn about Galactosemia.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Metabolic SyndromeMs. Wareth isExperienced. Learn about Metabolic Syndrome.
- Multiple Carboxylase DeficiencyMs. Wareth isExperienced. Learn about Multiple Carboxylase Deficiency.
- Neonatal HypothyroidismMs. Wareth isExperienced. Learn about Neonatal Hypothyroidism.
- Ovarian CystsMs. Wareth isExperienced. Learn about Ovarian Cysts.
- Polycystic Ovary SyndromeMs. Wareth isExperienced. Learn about Polycystic Ovary Syndrome.