Overview
Aileen Clarke practices practicing medicine in Oxford, United Kingdom.
Ms. Clarke is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Chromosome 13q Duplication, Trisomy 13, and Hip Replacement.
She is actively involved in clinical research, co-authoring 136 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 Aileen E. Clarke
Is Aileen E. Clarke a top-rated expert for Tyrosinemia Type 1?
MediFind is an objective health platform that identifies experts based on real-world data. Aileen E. Clarke is classified as an Advanced expert for Tyrosinemia Type 1, 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 Aileen E. Clarke participate in research or clinical trials?
Yes. Aileen E. Clarke has published 135 articles and abstracts on conditions like Tyrosinemia Type 1. You can view a list of Aileen E. Clarke'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
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Tyrosinemia Type 1Ms. Clarke isAdvanced. Learn about Tyrosinemia Type 1.
- Experienced
- Breast CancerMs. Clarke isExperienced. Learn about Breast Cancer.
- Chromosome 13q DuplicationMs. Clarke isExperienced. Learn about Chromosome 13q Duplication.
- Crohn's DiseaseMs. Clarke isExperienced. Learn about Crohn's Disease.
- Down SyndromeMs. Clarke isExperienced. Learn about Down Syndrome.
- Hip ReplacementMs. Clarke isExperienced. Learn about Hip Replacement.
- HIV/AIDSMs. Clarke isExperienced. Learn about HIV/AIDS.
- MalnutritionMs. Clarke isExperienced. Learn about Malnutrition.
- Mitochondrial Trifunctional Protein Deficiency
- NecrosisMs. Clarke isExperienced. Learn about Necrosis.
- OsteoarthritisMs. Clarke isExperienced. Learn about Osteoarthritis.
- Protein DeficiencyMs. Clarke isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisMs. Clarke isExperienced. Learn about Rhabdomyolysis.
- Severe Acute Respiratory Syndrome (SARS)
- Strep ThroatMs. Clarke isExperienced. Learn about Strep Throat.
- Streptococcal Group B InfectionMs. Clarke isExperienced. Learn about Streptococcal Group B Infection.
- Trisomy 13Ms. Clarke isExperienced. Learn about Trisomy 13.
- Trisomy 18Ms. Clarke isExperienced. Learn about Trisomy 18.
- Viral GastroenteritisMs. Clarke isExperienced. Learn about Viral Gastroenteritis.