Overview
Maggie Williams practices practicing medicine in Bristol, United Kingdom.
Ms. Williams is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Alport Syndrome, Gingival Fibromatosis with Hypertrichosis, KBG Syndrome, Facioscapulohumeral Muscular Dystrophy (FSHD), and Kidney Transplant.
She is actively involved in clinical research, co-authoring 43 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 Maggie M. Williams
Is Maggie M. Williams a top-rated expert for Alport Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Maggie M. Williams is classified as an Advanced expert for Alport Syndrome, 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 Maggie M. Williams participate in research or clinical trials?
Yes. Maggie M. Williams has published 43 articles and abstracts on conditions like Alport Syndrome. You can view a list of Maggie M. Williams'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
- Alport SyndromeMs. Williams isAdvanced. Learn about Alport Syndrome.
- Gingival Fibromatosis with Hypertrichosis
- Experienced
- Barth SyndromeMs. Williams isExperienced. Learn about Barth Syndrome.
- Brachydactyly Mononen TypeMs. Williams isExperienced. Learn about Brachydactyly Mononen Type.
- Cantu SyndromeMs. Williams isExperienced. Learn about Cantu Syndrome.
- ChondrodystrophyMs. Williams isExperienced. Learn about Chondrodystrophy.
- Chronic Kidney DiseaseMs. Williams isExperienced. Learn about Chronic Kidney Disease.
- Classic GalactosemiaMs. Williams isExperienced. Learn about Classic Galactosemia.
- CraniosynostosisMs. Williams isExperienced. Learn about Craniosynostosis.
- Defective Apolipoprotein B-100Ms. Williams isExperienced. Learn about Defective Apolipoprotein B-100.
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Familial HypercholesterolemiaMs. Williams isExperienced. Learn about Familial Hypercholesterolemia.
- Focal Segmental GlomerulosclerosisMs. Williams isExperienced. Learn about Focal Segmental Glomerulosclerosis.
- Galactokinase DeficiencyMs. Williams isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Williams isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Williams isExperienced. Learn about Galactosemia.
- GliomaMs. Williams isExperienced. Learn about Glioma.
- Gliomatosis CerebriMs. Williams isExperienced. Learn about Gliomatosis Cerebri.
- High CholesterolMs. Williams isExperienced. Learn about High Cholesterol.
- Hirsutism in WomenMs. Williams isExperienced. Learn about Hirsutism in Women.
- KBG SyndromeMs. Williams isExperienced. Learn about KBG Syndrome.
- Kidney TransplantMs. Williams isExperienced. Learn about Kidney Transplant.
- Nephrotic SyndromeMs. Williams isExperienced. Learn about Nephrotic Syndrome.
- Schwartz-Jampel SyndromeMs. Williams isExperienced. Learn about Schwartz-Jampel Syndrome.
- Spondyloepimetaphyseal Dysplasia Strudwick Type
- Ventricular FibrillationMs. Williams isExperienced. Learn about Ventricular Fibrillation.
- X-Linked Spondyloepiphyseal Dysplasia TardaMs. Williams isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.