Overview
Lynette Fairbanks practices practicing medicine in London, United Kingdom.
Ms. Fairbanks is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Hereditary Xanthinuria, Molybdenum Cofactor Deficiency (MoCD), Purine Nucleoside Phosphorylase Deficiency, and Severe Combined Immunodeficiency (SCID).
She is actively involved in clinical research, co-authoring 35 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 Lynette D. Fairbanks
Is Lynette D. Fairbanks a top-rated expert for Hereditary Xanthinuria?
MediFind is an objective health platform that identifies experts based on real-world data. Lynette D. Fairbanks is classified as an Distinguished expert for Hereditary Xanthinuria, 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 Lynette D. Fairbanks participate in research or clinical trials?
Yes. Lynette D. Fairbanks has published 35 articles and abstracts on conditions like Hereditary Xanthinuria. You can view a list of Lynette D. Fairbanks'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
- Distinguished
- Hereditary XanthinuriaMs. Fairbanks isDistinguished. Learn about Hereditary Xanthinuria.
- Molybdenum Cofactor Deficiency (MoCD)Ms. Fairbanks isDistinguished. Learn about Molybdenum Cofactor Deficiency (MoCD).
- Advanced
- Purine Nucleoside Phosphorylase Deficiency
- Experienced
- Adenine Phosphoribosyltransferase DeficiencyMs. Fairbanks isExperienced. Learn about Adenine Phosphoribosyltransferase Deficiency.
- Adenosine Deaminase DeficiencyMs. Fairbanks isExperienced. Learn about Adenosine Deaminase Deficiency.
- Adenylosuccinate Lyase DeficiencyMs. Fairbanks isExperienced. Learn about Adenylosuccinate Lyase Deficiency.
- GoutMs. Fairbanks isExperienced. Learn about Gout.
- HypotoniaMs. Fairbanks isExperienced. Learn about Hypotonia.
- Kidney StonesMs. Fairbanks isExperienced. Learn about Kidney Stones.
- MELAS SyndromeMs. Fairbanks isExperienced. Learn about MELAS Syndrome.
- Severe Combined Immunodeficiency (SCID)Ms. Fairbanks isExperienced. Learn about Severe Combined Immunodeficiency (SCID).
- Sulfite Oxidase DeficiencyMs. Fairbanks isExperienced. Learn about Sulfite Oxidase Deficiency.