Grazia Bossi

A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children

Marco Gattorno, Maria Pia Sormani, Andrea D’Osualdo et al. · Arthritis & Rheumatism · 2008 · 190 citations

Medicine, Molecular Genetics, Pediatrics +15

Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome

Caterina Cancrini, Pamela Puliafito, M. Cristina Digilio et al. · The Journal of Pediatrics · 2014 · 167 citations

Life Sciences, Genetics, Molecular Genetics +14

Long‐term clinical profile of children with the low‐penetrance R92Q mutation of the <i>TNFRSF1A</i> gene

MA Pelagatti, Roberta Caorsi, Marco Cattalini et al. · Arthritis & Rheumatism · 2011 · 105 citations · Full text

Medicine, Child Health, Pediatrics +12

A Prospective Study on Children with Initial Diagnosis of Transient Hypogammaglobulinemia of Infancy: Results from the Italian Primary Immunodeficiency Network

Viviana Moschese, Simona Graziani, Maria Antonietta Avanzini et al. · International Journal of Immunopathology and Pharmacology · 2008 · 75 citations · Full text

Life Sciences, Immunology, Pediatrics +15

Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome

Davide Montin, Agostina Marolda, Francesco Licciardi et al. · The Journal of Allergy and Clinical Immunology In Practice · 2019 · 53 citations · Full text

Life Sciences, Genetics, Immunology +13