Maria Luisa Romiti

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 · 164 citations

Down Syndrome, Clinical Disorders, Mendelian Disorder +6

Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome)

Andrea Finocchi, Silvia Di Cesare, Maria Luisa Romiti et al. · Pediatric Allergy and Immunology · 2006 · 84 citations · Full text

Recurrent Infections, Immunodeficiencies, Humoral Response +18

Post-Natal Ontogenesis of the T-Cell Receptor CD4 and CD8 Vβ Repertoire and Immune Function in Children with DiGeorge Syndrome

Caterina Cancrini, Maria Luisa Romiti, Andrea Finocchi et al. · Journal of Clinical Immunology · 2005 · 40 citations · Full text

Developmental Biology, Digeorge Syndrome, T-cell Receptor Cd4 +14

Immune deficiency caused by impaired expression of nuclear factor-κB essential modifier (NEMO) because of a mutation in the 5′ untranslated region of the NEMO gene

Jana L. Mooster, Caterina Cancrini, Alessandra Simonetti et al. · Journal of Allergy and Clinical Immunology · 2010 · 37 citations

Immunodeficiencies, Genetics, Immunology +18

Prognostic Value of the Stromal Cell–Derived Factor 1 3′A Mutation in Pediatric Human Immunodeficiency Virus Type 1 Infection

Eleonora Tresoldi, Maria Luisa Romiti, Michele Boniotto et al. · The Journal of Infectious Diseases · 2002 · 34 citations · Full text