Overview
Matilda Jackson practices in Adelaide, Australia. Ms. Jackson is rated as an Experienced expert by MediFind in the treatment of X-Linked Spondyloepiphyseal Dysplasia Tarda. Her top areas of expertise are Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Seckel Syndrome, West Syndrome, and Mucopolysaccharidoses (MPS).
Her clinical research consists of co-authoring 26 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 X-Linked Spondyloepiphyseal Dysplasia Tarda.
Locations
Adelaide, SA, Australia
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
- Distinguished
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Advanced
- Seckel SyndromeMs. Jackson isAdvanced. Learn about Seckel Syndrome.
- West SyndromeMs. Jackson isAdvanced. Learn about West Syndrome.
- Experienced
- Absence SeizureMs. Jackson isExperienced. Learn about Absence Seizure.
- Acromicric DysplasiaMs. Jackson isExperienced. Learn about Acromicric Dysplasia.
- Autosomal Recessive Primary MicrocephalyMs. Jackson isExperienced. Learn about Autosomal Recessive Primary Microcephaly.
- Brachydactyly Mononen TypeMs. Jackson isExperienced. Learn about Brachydactyly Mononen Type.
- Caffey DiseaseMs. Jackson isExperienced. Learn about Caffey Disease.
- ChondrodystrophyMs. Jackson isExperienced. Learn about Chondrodystrophy.