Overview
Mattia Gentile practices practicing medicine in Bari, Italy.
Gentile is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Schimke Immuno-Osseous Dysplasia, Kozlowski Warren Fisher Syndrome, Brittle Cornea Syndrome, and Schwartz-Jampel Syndrome.
They are actively involved in clinical research, co-authoring 62 peer reviewed articles.
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 Mattia T. Gentile
Is Mattia T. Gentile a top-rated expert for Schimke Immuno-Osseous Dysplasia?
MediFind is an objective health platform that identifies experts based on real-world data. Mattia T. Gentile is classified as an Advanced expert for Schimke Immuno-Osseous Dysplasia, 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 Mattia T. Gentile participate in research or clinical trials?
Yes. Mattia T. Gentile has published 62 articles and abstracts on conditions like Schimke Immuno-Osseous Dysplasia. You can view a list of Mattia T. Gentile'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
- Brittle Cornea SyndromeGentile isAdvanced. Learn about Brittle Cornea Syndrome.
- Kozlowski Warren Fisher Syndrome
- Schimke Immuno-Osseous Dysplasia
- Experienced
- Absence SeizureGentile isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeGentile isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AcrocephalopolydactylyGentile isExperienced. Learn about Acrocephalopolydactyly.
- Acromicric DysplasiaGentile isExperienced. Learn about Acromicric Dysplasia.
- Acute Myeloid Leukemia (AML)Gentile isExperienced. Learn about Acute Myeloid Leukemia (AML).
- AnhidrosisGentile isExperienced. Learn about Anhidrosis.
- Apert SyndromeGentile isExperienced. Learn about Apert Syndrome.
- AstigmatismGentile isExperienced. Learn about Astigmatism.
- Autism Spectrum DisorderGentile isExperienced. Learn about Autism Spectrum Disorder.
- Autonomic NeuropathyGentile isExperienced. Learn about Autonomic Neuropathy.
- Brachydactyly Mononen TypeGentile isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyGentile isExperienced. Learn about Chondrodystrophy.
- Chromosome 13q DuplicationGentile isExperienced. Learn about Chromosome 13q Duplication.
- Chromosome 18q DuplicationGentile isExperienced. Learn about Chromosome 18q Duplication.
- Cleidocranial DysplasiaGentile isExperienced. Learn about Cleidocranial Dysplasia.
- Cortical DysplasiaGentile isExperienced. Learn about Cortical Dysplasia.
- FibroadenomaGentile isExperienced. Learn about Fibroadenoma.
- Generalized Tonic-Clonic SeizureGentile isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Hajdu-Cheney SyndromeGentile isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hereditary AtaxiaGentile isExperienced. Learn about Hereditary Ataxia.
- Hereditary Multiple Osteochondromas
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- HydrocephalusGentile isExperienced. Learn about Hydrocephalus.
- Hypertrophic Cardiomyopathy (HCM)Gentile isExperienced. Learn about Hypertrophic Cardiomyopathy (HCM).
- HypothyroidismGentile isExperienced. Learn about Hypothyroidism.
- HypotoniaGentile isExperienced. Learn about Hypotonia.
- Intrauterine Growth RestrictionGentile isExperienced. Learn about Intrauterine Growth Restriction.
- Lactic AcidosisGentile isExperienced. Learn about Lactic Acidosis.
- Lennox-Gastaut Syndrome (LGS)Gentile isExperienced. Learn about Lennox-Gastaut Syndrome (LGS).
- MesotheliomaGentile isExperienced. Learn about Mesothelioma.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyGentile isExperienced. Learn about Microcephaly.
- MosaicismGentile isExperienced. Learn about Mosaicism.
- Nephrotic SyndromeGentile isExperienced. Learn about Nephrotic Syndrome.
- Noonan SyndromeGentile isExperienced. Learn about Noonan Syndrome.
- OsteochondromaGentile isExperienced. Learn about Osteochondroma.
- Pfeiffer SyndromeGentile isExperienced. Learn about Pfeiffer Syndrome.
- PolyhydramniosGentile isExperienced. Learn about Polyhydramnios.
- Primary Immunodeficiency (PID)Gentile isExperienced. Learn about Primary Immunodeficiency (PID).
- Primary Lateral SclerosisGentile isExperienced. Learn about Primary Lateral Sclerosis.
- Pulmonary Valve StenosisGentile isExperienced. Learn about Pulmonary Valve Stenosis.
- RASopathiesGentile isExperienced. Learn about RASopathies.
- Rhizomelic SyndromeGentile isExperienced. Learn about Rhizomelic Syndrome.
- Saethre-Chotzen SyndromeGentile isExperienced. Learn about Saethre-Chotzen Syndrome.
- Schwartz-Jampel SyndromeGentile isExperienced. Learn about Schwartz-Jampel Syndrome.
- SeizuresGentile isExperienced. Learn about Seizures.
- Short Stature (Growth Disorders)Gentile isExperienced. Learn about Short Stature (Growth Disorders).
- SyndactylyGentile isExperienced. Learn about Syndactyly.
- Trisomy 13Gentile isExperienced. Learn about Trisomy 13.
- Trisomy 18Gentile isExperienced. Learn about Trisomy 18.
- X-Linked Spondyloepiphyseal Dysplasia Tarda