Overview
Luigi Notarangelo is a Pediatric Allergy and Immunologist in Boston, Massachusetts. Dr. Notarangelo and is rated as an Experienced provider by MediFind in the treatment of Congenital Toxoplasmosis. His top areas of expertise are Severe Combined Immunodeficiency (SCID), X-Linked Severe Combined Immunodeficiency, Wiskott-Aldrich Syndrome, and Immunodeficiency with Hyper IgM Type 1.
His clinical research consists of co-authoring 449 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Congenital Toxoplasmosis.
Insurance
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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. Providers 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.
1 Clinical Trials
Anthony Hayward is a Pediatric Allergy and Immunologist in Providence, Rhode Island. Dr. Hayward and is rated as an Experienced provider by MediFind in the treatment of Congenital Toxoplasmosis. His top areas of expertise are Pignata Guarino Syndrome, Common Variable Immune Deficiency, Infantile Neutropenia, and Congenital Toxoplasmosis.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Elite
- Severe Combined Immunodeficiency (SCID)
- Wiskott-Aldrich Syndrome
- X-Linked Severe Combined Immunodeficiency
- Distinguished
- Cartilage-Hair Hypoplasia
- Chronic Granulomatous Disease
- Immunodeficiency with Hyper IgM Type 1
- Infantile Neutropenia
- Omenn Syndrome
- Purine Nucleoside Phosphorylase Deficiency
- Advanced
- Adenosine Deaminase Deficiency
- Common Variable Immune Deficiency
- Congenital Athymia
- Immune Defect due to Absence of Thymus
- Pignata Guarino Syndrome
- Pulmonary Alveolar Proteinosis
- Experienced
- Activated PI3K Delta Syndrome (APDS)
- Alpha Mannosidosis
- Autosomal Dominant Hyper IgE Syndrome
- Chronic Graft Versus Host Disease (cGvHD)
- Congenital Toxoplasmosis
- Cri-Du-Chat Syndrome