Overview
Maria Marinelli practices practicing medicine in Reggio Nell'emilia, Italy.
Ms. Marinelli is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Chromosome 11 Uniparental Disomy, Multiple Pterygium Syndrome, Epidermal Nevus, and Preaxial Polydactyly Type 1.
She is actively involved in clinical research, co-authoring 14 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 Maria Marinelli
Is Maria Marinelli a top-rated expert for Chromosome 11 Uniparental Disomy?
MediFind is an objective health platform that identifies experts based on real-world data. Maria Marinelli is classified as an Advanced expert for Chromosome 11 Uniparental Disomy, 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 Maria Marinelli participate in research or clinical trials?
Yes. Maria Marinelli has published 14 articles and abstracts on conditions like Chromosome 11 Uniparental Disomy. You can view a list of Maria Marinelli'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
- Chromosome 11 Uniparental DisomyMs. Marinelli isAdvanced. Learn about Chromosome 11 Uniparental Disomy.
- Experienced
- Achalasia Microcephaly SyndromeMs. Marinelli isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Arthrogryposis Multiplex CongenitaMs. Marinelli isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Cat Eye SyndromeMs. Marinelli isExperienced. Learn about Cat Eye Syndrome.
- Congenital ContracturesMs. Marinelli isExperienced. Learn about Congenital Contractures.
- Cortical DysplasiaMs. Marinelli isExperienced. Learn about Cortical Dysplasia.
- Cri-Du-Chat SyndromeMs. Marinelli isExperienced. Learn about Cri-Du-Chat Syndrome.
- Epidermal NevusMs. Marinelli isExperienced. Learn about Epidermal Nevus.
- Exstrophy of the BladderMs. Marinelli isExperienced. Learn about Exstrophy of the Bladder.
- Intrauterine Growth RestrictionMs. Marinelli isExperienced. Learn about Intrauterine Growth Restriction.
- LissencephalyMs. Marinelli isExperienced. Learn about Lissencephaly.
- MicrocephalyMs. Marinelli isExperienced. Learn about Microcephaly.
- MosaicismMs. Marinelli isExperienced. Learn about Mosaicism.
- Multiple Pterygium SyndromeMs. Marinelli isExperienced. Learn about Multiple Pterygium Syndrome.
- PolydactylyMs. Marinelli isExperienced. Learn about Polydactyly.
- Preaxial Polydactyly Type 1Ms. Marinelli isExperienced. Learn about Preaxial Polydactyly Type 1.
- PterygiumMs. Marinelli isExperienced. Learn about Pterygium.
- Trisomy 12 MosaicismMs. Marinelli isExperienced. Learn about Trisomy 12 Mosaicism.
- Ventricular Septal DefectsMs. Marinelli isExperienced. Learn about Ventricular Septal Defects.
- Wolf-Hirschhorn SyndromeMs. Marinelli isExperienced. Learn about Wolf-Hirschhorn Syndrome.
- X-Linked Retinal DysplasiaMs. Marinelli isExperienced. Learn about X-Linked Retinal Dysplasia.