L. Notarangelo

发表

X‐linked immunodeficiency with hyper‐IgM (XHIM)

L. Notarangelo, L. D. Notarangelo, A. R. Hayward, 2000, Clinical and experimental immunology.

The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM

D. Allen, L. Notarangelo, R. Geha, 1998, Nature.

NTB-A [correction of GNTB-A], a novel SH2D1A-associated surface molecule contributing to the inability of natural killer cells to kill Epstein-Barr virus-infected B cells in X-linked lymphoproliferative disease.

L. Notarangelo, R. Biassoni, L. Moretta, 2001, The Journal of experimental medicine.

Absence of xid mutation in X-linked agammaglobulinaemia

W. Paul, I. Vořechovský, L. Hammarström, 1993, The Lancet.

Nodular regenerative hyperplasia in X-linked agammaglobulinemia: an underestimated and severe complication.

S. Holland, D. Kleiner, G. Uzel, 2021, The Journal of allergy and clinical immunology.

l spectrum of X-linked hyper-IgM syndrome

M. Peitsch, Lennart Hammarstrom, A. Finn, 2004 .

Production and persistence of specific antibodies in COVID-19 patients with hematologic malignancies: role of rituximab

K. Dobbs, J. Chiorini, H. Su, 2021, Blood Cancer Journal.

Wiskott–Aldrich syndrome: another piece in the puzzle

L. Mori, L. D. Notarangelo, L. Notarangelo, 2005, Clinical and experimental immunology.

X‐chromosome inactivation analysis in a female carrier of FOXP3 mutation

R. Badolato, S. Ferrari, M. Boniotto, 2002, Clinical and experimental immunology.

Autoantibodies Detected in MIS-C Patients due to Administration of Intravenous Immunoglobulin

L. Notarangelo, K. Dobbs, J. Chiorini, 2021, medRxiv.

Mapping of the X linked form of hyper IgM syndrome (HIGM1)

R. Levinsky, A. Read, S. Malcolm, 1993, Journal of medical genetics.

Prenatal diagnosis of X‐linked hyper‐IGM syndrome by direct detection of mutation Q220X in the CD40L gene using PCR‐mediated site directed mutagenesis

R. Gershoni-baruch, Amos Etzioni, L. Kasinetz, 2000, Prenatal diagnosis.