D. De Mattia

Catamenial hemoptysis from endobronchial endometriosis in a child with type 1 von Willebrand disease

P. Giordano, A. Cimmino, M. Loizzi, 2007, Pediatric pulmonology.

Defective surface expression of attractin on T cells in patients with common variable immunodeficiency (CVID)

C. Pignata, N. Pozzi, J. Duke-Cohan, 2001, Clinical and experimental immunology.

14q13 distal microdeletion encompassing NKX2‐1 and PAX9: Patient report and refinement of the associated phenotype

R. Ficarella, N. Laforgia, M. Gentile, 2016, American journal of medical genetics. Part A.

Reduced Interleukin-5 Production by Peripheral Cd4+ T Cells in Common Variable Immunodeficiency Patients

P. Giordano, G. Lassandro, G. C. Del Vecchio, 2008 .

Lymphatic Malformation in Newborns as the First Sign of Diffuse Lymphangiomatosis: Successful Treatment with Sirolimus

N. Laforgia, D. Martinelli, F. Schettini, 2015, Neonatology.

Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization.

L. Notarangelo, S. Giliani, F. Candotti, 2000, Clinical immunology.

Langerhans cell histiocytosis in a pediatric patient with thrombocytopenia-absent radius syndrome and 1q21.1 deletion: case report and proposal of a rapid molecular diagnosis of 1q21.1 deletion

N. Santoro, P. Giordano, L. Giordani, 2011, Immunopharmacology and immunotoxicology.