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International Archives of Allergy and Immunology|January 1, 1993
Clinical manifestations of allergy and their relation to HIV infectionT Dikeacou, A Katsambas, W Lowenstein, et al.Frontiers in Medicine|December 17, 2020
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 CasesAntonio Mastrangelo, Marisa Giani, Elena Groppali, et al.Respiratory Research|June 16, 2023
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorderLaura Bergantini, Margherita Baldassarri, Miriana d'Alessandro, et al.Journal of Neurointerventional Surgery|October 16, 2013
Endovascular treatment of unruptured and ruptured brain arteriovenous malformations with Onyx18: a monocentric series of 84 patientsArturo Consoli, Giulia Scarpini, Andrea Rosi, et al.Journal of Human Genetics|January 20, 2007
Frequency of the LRRK2 G2019S mutation in Italian patients affected by Parkinson's diseaseTiziana Squillaro, Franca Cambi, Giuseppe Ciacci, et al.Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|April 20, 2004
Saturation and electron-beam lifetime in a storage ring free-electron laserR Bartolini, G Dattoli, L Giannessi, et al.American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.European Journal of Human Genetics : EJHG|June 15, 2000
Preserved speech variant is allelic of classic Rett syndromeC De Bona, M Zappella, G Hayek, et al.Nature Communications|October 23, 2019
Author Correction: A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrierAstgik Petrosyan, Paolo Cravedi, Valentina Villani, et al.European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.Pageof 63