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Cytogenetics and Cell Genetics|January 1, 1997
Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinomaS Bekri, J Adélaïde, S Merscher, et al.
International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.
Human Immunology|April 21, 1998
Repertoire breadth of human CD4+ T cells specific for HIV gp120 and p66 (primary antigens) or for PPD and tetanus toxoid (secondary antigens)G Li Pira, L Oppezzi, M Seri, et al.
Arthritis and Rheumatism|January 13, 2011
Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A geneM A Pelagatti, A Meini, R Caorsi, et al.
Clinical and Experimental Immunology|May 2, 2002
Preservation of clonal heterogeneity of the Pneumocystis carinii-specific CD4 T cell repertoire in HIV infected, asymptomatic individualsG Li Pira, D Fenoglio, L Bottone, et al.
American Journal of Human Genetics|February 11, 1999
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophyM Seri, R Cusano, P Forabosco, et al.
Human Genetics|March 10, 1999
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopmentM Seri, G Martucciello, L Paleari, et al.
Clinical Genetics|September 27, 2007
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander diseaseF Caroli, R Biancheri, M Seri, et al.
Arthritis and Rheumatism|March 2, 2011
Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutationS Borghini, S Tassi, S Chiesa, et al.
Arthritis and Rheumatism|June 3, 2008
A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in childrenM Gattorno, M P Sormani, A D'Osualdo, et al.
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