M. Zanussi

发表

Loss of mismatched HLA in leukemia after stem-cell transplantation.

Federica Torri, C. Barlassina, M. Roncarolo, 2009, The New England journal of medicine.

Genomic Loss of the Mismatched HLA Locus in Leukemia Is a Major Mechanism of in Vivo Escape from T Cell Immunosurveillance Following Haploidentical HSCT

M. Roncarolo, C. Bordignon, F. Ciceri, 2008 .

Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination

M. Ferrari, A. Forabosco, D. Coviello, 2005, Prenatal diagnosis.

Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency

A. Mortellaro, A. Aiuti, M. Ponzoni, 2022, Frontiers in Immunology.

Association of LOXIN, a new functional splicing isoform of the OLR1 gene, with severity and prognostic localization of critical coronary artery stenoses

M. Ferrari, A. Margonato, A. Cappelletti, 2014, Journal of cardiovascular medicine.

Efficacy of lentivirus‐mediated gene therapy in an Omenn syndrome recombination‐activating gene 2 mouse model is not hindered by inflammation and immune dysregulation

L. Notarangelo, K. Dobbs, G. Wagemaker, 2017, The Journal of allergy and clinical immunology.

Capillary zone electrophoresis in polymer networks of polymerase chain reaction-amplified oligonucleotides: the case of congenital adrenal hyperplasia.

M. Ferrari, P. Righetti, C. Gelfi, 1994, Journal of chromatography. B, Biomedical applications.

Case Report: Efficacy of Rituximab in a Patient With Familial Mediterranean Fever and Multiple Sclerosis

N. Bresolin, D. Galimberti, E. Scarpini, 2021, Frontiers in Neurology.

Genomic typing for patient-specific human leukocyte antigen-alleles is an efficient tool for relapse detection of high-risk hematopoietic malignancies after stem cell transplantation from alternative donors

C. Bordignon, F. Ciceri, A. Palini, 2008, Leukemia.

Case report: Complex arterial findings in vascular ehlers-danlos syndrome with a novel COL3A1 variant and death at young age

C. Pappone, M. Chessa, Paola Carrera, 2023, Frontiers in Cardiovascular Medicine.