Overview
Madeline Reilly practices in London, United Kingdom. Ms. Reilly is rated as an Experienced expert by MediFind in the treatment of Microcephaly with Spastic Quadriplegia. Her top areas of expertise are Charcot-Marie-Tooth Disease, Bilateral Renal Agenesis Dominant Type, Potter Syndrome, and Microcephaly.
Her clinical research consists of co-authoring 42 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Microcephaly with Spastic Quadriplegia.
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.
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
- Achalasia Microcephaly SyndromeMs. Reilly isAdvanced. Learn about Achalasia Microcephaly Syndrome.
- Bilateral Renal Agenesis Dominant Type
- Charcot-Marie-Tooth DiseaseMs. Reilly isAdvanced. Learn about Charcot-Marie-Tooth Disease.
- MicrocephalyMs. Reilly isAdvanced. Learn about Microcephaly.
- Potter SyndromeMs. Reilly isAdvanced. Learn about Potter Syndrome.
- Experienced
- Acromesomelic DysplasiaMs. Reilly isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux TypeMs. Reilly isExperienced. Learn about Acromesomelic Dysplasia Maroteaux Type.
- Aplasia Cutis CongenitaMs. Reilly isExperienced. Learn about Aplasia Cutis Congenita.
- Autosomal Recessive Primary Microcephaly