Renata R.
- Country
- Italy
- Department
- U.O.C. Neuropsichiatria Infantile
Research Overview
Data & Insights
Has run more than one trial at 32 of 36 partner sites.
Specializations
Neurodevelopmental and Movement Disorders
Clinical research activity in U.O.C. Neuropsichiatria Infantile includes therapeutic interest in childhood and adolescent neurological conditions, with attention to Tourette’s Disorder, juvenile idiopathic arthritis with neuropsychiatric relevance, and early Parkinson’s disease across pediatric and adult care pathways.
- Tourette’s Disorder
- Early Parkinson’s disease
- Multiple sclerosis
Interest also extends to disorders affecting motor control and central nervous system function, including multiple system atrophy, radiologically isolated syndrome, and neurogenic orthostatic hypotension.
Autoimmune and Inflammatory Diseases
The investigator is involved in clinical research on immune-mediated disorders with a strong therapeutic focus on atopic dermatitis, hidradenitis suppurativa, psoriasis, and connective tissue diseases such as systemic lupus erythematosus and systemic sclerosis.
- Atopic dermatitis
- Hidradenitis suppurativa
- Dermatomyositis
Additional therapeutic interest includes juvenile idiopathic arthritis, rheumatoid arthritis, Sjögren’s syndrome, and bullous pemphigoid, reflecting work in systemic inflammation and skin-immune disease management.
Respiratory and Interstitial Lung Disease
Research involvement covers chronic and progressive pulmonary disorders, with emphasis on asthma, chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis, and broader interstitial lung disease phenotypes.
- Asthma
- Idiopathic pulmonary fibrosis
- Chronic obstructive pulmonary disease
Therapeutic activity also includes pulmonary sarcoidosis, progressive pulmonary fibrosis, bronchiectasis, and cystic fibrosis, indicating interest in advanced respiratory care and disease-modifying treatment options.
Hematologic Malignancies and Bone Marrow Disorders
The investigator contributes to studies in acute lymphoblastic leukemia, acute myeloid leukemia, multiple myeloma, and lymphoma, with a therapeutic focus spanning pediatric and adult hematologic oncology.
- Acute lymphoblastic leukemia
- Multiple myeloma
- Follicular lymphoma
Additional areas include myelodysplastic syndrome, myelofibrosis, chronic lymphocytic leukemia, and paroxysmal nocturnal hemoglobinuria, highlighting involvement in marrow failure, clonal hematologic disease, and targeted hematology therapies.
Pediatric and Rare Genetic Disorders
Clinical interest also extends to pediatric rare diseases and inherited conditions, including Niemann-Pick disease type C1, tuberous sclerosis complex, neuroblastoma, and medulloblastoma.
- Niemann-Pick disease type C1
- Tuberous sclerosis complex
- Medulloblastoma
Research activity further includes juvenile idiopathic arthritis, Down syndrome–associated myeloid leukemia, and PMM2-CDG, reflecting engagement with complex childhood disorders requiring specialized therapeutic development.
Related Investigators
Researchers in similar fields or departments
Want to know more about this investigator?
We can share extended profile information and contact details.
Is something out of date?
Tell us what needs correcting and we'll update this profile.