Overview
Valentina Trevisan practices practicing medicine in Rome, Italy.
Ms. Trevisan is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses RASopathies, Chromosome 22 Duplication, Smith-Magenis Syndrome, and Chromosome 9p Deletion.
She is actively involved in clinical research, co-authoring 26 peer reviewed articles.
Gender
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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 Valentina Trevisan
Is Valentina Trevisan a top-rated expert for RASopathies?
MediFind is an objective health platform that identifies experts based on real-world data. Valentina Trevisan is classified as an Advanced expert for RASopathies, 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 Valentina Trevisan participate in research or clinical trials?
Yes. Valentina Trevisan has published 26 articles and abstracts on conditions like RASopathies. You can view a list of Valentina Trevisan'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 22 DuplicationMs. Trevisan isAdvanced. Learn about Chromosome 22 Duplication.
- Chromosome 9p DeletionMs. Trevisan isAdvanced. Learn about Chromosome 9p Deletion.
- Costello SyndromeMs. Trevisan isAdvanced. Learn about Costello Syndrome.
- RASopathiesMs. Trevisan isAdvanced. Learn about RASopathies.
- SchwannomatosisMs. Trevisan isAdvanced. Learn about Schwannomatosis.
- Smith-Magenis SyndromeMs. Trevisan isAdvanced. Learn about Smith-Magenis Syndrome.
- Experienced
- Acanthosis NigricansMs. Trevisan isExperienced. Learn about Acanthosis Nigricans.
- AchondroplasiaMs. Trevisan isExperienced. Learn about Achondroplasia.
- Aplasia Cutis CongenitaMs. Trevisan isExperienced. Learn about Aplasia Cutis Congenita.
- ApraxiaMs. Trevisan isExperienced. Learn about Apraxia.
- Beckwith-Wiedemann SyndromeMs. Trevisan isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Cafe-Au-Lait SpotsMs. Trevisan isExperienced. Learn about Cafe-Au-Lait Spots.
- Cardiofaciocutaneous SyndromeMs. Trevisan isExperienced. Learn about Cardiofaciocutaneous Syndrome.
- Chromosome 13q DuplicationMs. Trevisan isExperienced. Learn about Chromosome 13q Duplication.
- Clouston SyndromeMs. Trevisan isExperienced. Learn about Clouston Syndrome.
- Cold-Induced Sweating SyndromeMs. Trevisan isExperienced. Learn about Cold-Induced Sweating Syndrome.
- Ectodermal DysplasiasMs. Trevisan isExperienced. Learn about Ectodermal Dysplasias.
- GigantismMs. Trevisan isExperienced. Learn about Gigantism.
- HyperhidrosisMs. Trevisan isExperienced. Learn about Hyperhidrosis.
- Increased Head CircumferenceMs. Trevisan isExperienced. Learn about Increased Head Circumference.
- MacroglossiaMs. Trevisan isExperienced. Learn about Macroglossia.
- MosaicismMs. Trevisan isExperienced. Learn about Mosaicism.
- NeurofibromatosisMs. Trevisan isExperienced. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)Ms. Trevisan isExperienced. Learn about Neurofibromatosis Type 1 (NF1).
- Noonan SyndromeMs. Trevisan isExperienced. Learn about Noonan Syndrome.
- Short QT SyndromeMs. Trevisan isExperienced. Learn about Short QT Syndrome.
- Trisomy 13Ms. Trevisan isExperienced. Learn about Trisomy 13.