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Genes|April 30, 2021
Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly WomenMaria Monticelli, Bruno Hay Mele, Elisa Benetti, et al.BMC Nephrology|February 28, 2019
Non-collagen genes role in digenic Alport syndromeS Daga, C Fallerini, S Furini, et al.Journal of Medical Genetics|February 4, 2005
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasmsE Scala, F Ariani, F Mari, et al.Development (Cambridge, England)|April 21, 2016
Nucleolar activity and CENP-C regulate CENP-A and CAL1 availability for centromere assembly in meiosisLucretia Kwenda, Caitriona M Collins, Anna A Dattoli, et al.Kidney International|April 17, 2004
Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 geneChiara Pescucci, Francesca Mari, Ilaria Longo, et al.American Journal of Medical Genetics. Part A|July 9, 2011
Five patients with novel overlapping interstitial deletions in 8q22.2q22.3Alma Kuechler, Karen Buysse, Jill Clayton-Smith, et al.Gene Expression Patterns : GEP|December 17, 2005
Expression pattern of the maternally imprinted gene Gtl2 in the forebrain during embryonic development and adulthoodD McLaughlin, M Vidaki, E Renieri, et al.Annali Dell'Istituto Superiore Di Sanita|November 9, 2000
[Molecular genetics and bone diseases]A Renieri, N Giordano, S Geraci, et al.Klinische Monatsblatter Fur Augenheilkunde|January 21, 2011
[Chronic eyelid oedema and rosacea (Morbus Morbihan): diagnostic and therapeutic challenges]G Renieri, C Brochhausen, N Pfeiffer, et al.Klinische Monatsblatter Fur Augenheilkunde|April 19, 2019
The Use of Junfeng BFS Water (JBW) in Dry Eye SyndromeDieter Eisenmann, Yuying Liu, Giulia Renieri, et al.Pageof 2,638