CARANDO, Adriana

CARANDO, Adriana  

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A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease? 2020 Quarello, Paola; Garelli, Emanuela; Carando, Adriana; Cillario, Rebecca; Brusco, Alfredo; Giorgio, Elisa; Ferrante, Daniela; Corti, Paola; Zecca, Marco; Luciani, Matteo; Pierri, Filomena; Putti, Maria C; Cantarini, Maria E; Farruggia, Piero; Barone, Angelica; Cesaro, Simone; Russo, Giovanna; Fagioli, Franca; Dianzani, Irma; Ramenghi, Ugo
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia 2008 Ilenia Boria; Paola Quarello; Federica Avondo; Emanuela Garelli; Anna Aspesi; Adriana Carando; Maria Francesca Campagnoli; Irma Dianzani; Ugo Ramenghi
AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome 2006 SORASIO L; FERRERO G; GARELLI E; BRUNELLO G; MARTANO C; CARANDO A; BELLIGNI E; DIANZANI I; CIRILLO SILENGO M
Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients 2010 Ramenghi U ;Quarello P ;Garelli E ;Carando A;Lorenzati A ;Ansaldi G;Davitto M ;Boria I; Aspesi A ;Dianzani I
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 2004 QUARELLO P; CAMPAGNOLI MF; GARELLI E; CARANDO A; CRESCENZIO N; DORIA A; MARTINO S; RENGA D; U. RAMENGHI; DIANZANI I
Le basi genetiche di una ribosomopatia: un database per l'anemia di Diamond-Blackfan 2009 Boria I; Garelli E; Quarello P; Aspesi A; Carando A; Massano D; Dianzani I; Ramenghi U.
Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome. 2011 Prontera P; Garelli E; Isidori I; Mencarelli A; Carando A; Silengo MC; Donti E.
UN DATABASE PER L’ANEMIA DI DIAMOND-BLACKFAN 2010 Boria I; Garelli E; Quarello P;Aspesi A; Carando A; Lorenzati A; Ansaldi G; Davitto M; Dianzani I; Ramenghi U
Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcification 2019 Giorgio, Elisa; Garelli, Emanuela; Carando, Adriana; Bellora, Stefania; Rubino, Elisa; Quarello, Paola; Sirchia, Fabio; Marrama, Federico; Gallone, Salvatore; Grosso, Enrico; Pasini, Barbara; Massa, Roberto; Brussino, Alessandro; Brusco, Alfredo
Diamond-Blackfan anemia: genotype-phenotype correlation in Italian patients with RPL5 and RPL11 mutations 2010 Quarello P; Garelli E; Carando A; Brusco A; Calabrese R; Dufour C; Longoni D; Misuraca A; Vinti L; Aspesi A; Biondini L; Loreni F; Dianzani I; Ramenghi U
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. 2000 U. RAMENGHI; CAMPAGNOLI MF; GARELLI E; CARANDO A; BRUSCO A; BAGNARA GP; STRIPPOLI PL; IZZI GC; BRANDALISE S; RICCARDI R; DIANZANI I
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family 2006 CAMPAGNOLI MF; PUCCI A; GARELLI E; CARANDO A; DEFILIPPI C; LALA R; INGROSSO G; DIANZANI I; FORNI M; RAMENGHI U
HDR syndrome: a novel "de novo" mutation in GATA3 gene. 2009 Ferraris S; Del Monaco AG; Garelli E; Carando A; De Vito B; Pappi P; Lala R; Ponzone A.
High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay 2012 P. Quarello;E. Garelli;A. Brusco;A. Carando;C. Mancini;P. Pappi;L. Vinti;J. Svahn;I. Dianzani;U. Ramenghi
High frequency of RPL5 and RPL11 gene mutation in Italians patients with Diamond-Blackfan anemia (DBA) 2009 Dianzani I; Ramenghi U; Quarello P; Garelli E; Carando A; Campagnoli MF; Brusco A.
Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations 2008 Zavattaro E; Azzimonti B; Mondini M; De Andrea M; Borgogna C; Dell'Oste V; Ferretti M; Nicola S; Cappellano G; Carando A; Leigheb G; Landolfo S; Dianzani U; Gariglio M.
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein 2005 CHIOCCHETTI A; GIBELLO L; CARANDO A; ASPESI A; SECCO P; GARELLI E; LORENI F; ANGELINI M; BIAVA A; DAHL N; DIANZANI U; RAMENGHI U; SANTORO C; DIANZANI I
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype. 2014 Parrella S; Aspesi A; Quarello P; Garelli E; Pavesi E; Carando A; Nardi M; Ellis SR; Ramenghi U; Dianzani I.
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 2004 CAMPAGNOLI MF; GARELLI E; QUARELLO P; CARANDO A; VAROTTO S; NOBILI B; LONGONI D; PECILE V; ZECCA M; DUFOUR C; RAMENGHI U; DIANZANI I
Multiplex Ligation-dependent Probe Amplification (MLPA) enhances molecular diagnosis of Diamond Blackfan Anemia due to RPS19 deficiency 2008 Quarello, Paola; Garelli, Emanuela; Brusco, Alfredo; Carando, Adriana; Pappi, Patrizia; Barberis, Marco; Coletti, Valentina; Campagnoli, Maria Francesca; Dianzani, Irma; Ramenghi, Ugo