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Adriana Carando

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Disorders

Physiology

Chemicals & Drugs

Procedures

DNA Mutational Analysis

Geographic Areas

Italy

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Publications

TOP 3
Ferraris Silvio; Del Monaco Angelo Giovanni; Garelli Emanuela; Carando Adriana; De Vito Barbara; Pappi Patrizia; Lala Roberto; Ponzone Alberto
HDR syndrome: a novel "de novo" mutation in GATA3 gene.
Quarello Paola; Garelli Emanuela; Brusco Alfredo; Carando Adriana; Pappi Patrizia; Barberis Marco; Coletti Valentina; Campagnoli Maria Francesca; Dianzani Irma; Ramenghi Ugo
Multiplex ligation-dependent probe amplification enhances molecular diagnosis of Diamond-Blackfan anemia due to RPS19 deficiency.
Boria Ilenia; Quarello Paola; Avondo Federica; Garelli Emanuela; Aspesi Anna; Carando Adriana; Campagnoli Maria Francesca; Dianzani Irma; Ramenghi Ugo
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia.

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All Publications

2009: Ferraris Silvio; Del Monaco Angelo Giovanni; Garelli Emanuela; Carando Adriana; De Vito Barbara; Pappi Patrizia; Lala Roberto; Ponzone Alberto
HDR syndrome: a novel "de novo" mutation in GATA3 gene.
American journal of medical genetics. Part A 2009;149A(4):770-5.
2008: Quarello Paola; Garelli Emanuela; Brusco Alfredo; Carando Adriana; Pappi Patrizia; Barberis Marco; Coletti Valentina; Campagnoli Maria Francesca; Dianzani Irma; Ramenghi Ugo
Multiplex ligation-dependent probe amplification enhances molecular diagnosis of Diamond-Blackfan anemia due to RPS19 deficiency.
Haematologica 2008;93(11):1748-50.
2008: Boria Ilenia; Quarello Paola; Avondo Federica; Garelli Emanuela; Aspesi Anna; Carando Adriana; Campagnoli Maria Francesca; Dianzani Irma; Ramenghi Ugo
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia.
Human mutation 2008;29(11):E263-70.
2008: Campagnoli Maria Francesca; Ramenghi Ugo; Armiraglio Marta; Quarello Paola; Garelli Emanuela; Carando Adriana; Avondo Federica; Pavesi Elisa; Fribourg Sébastien; Gleizes Pierre-Emmanuel; Loreni Fabrizio; Dianzani Irma
RPS19 mutations in patients with Diamond-Blackfan anemia.
Human mutation 2008;29(7):911-20.
2008: Zavattaro Elisa; Azzimonti Barbara; Mondini Michele; De Andrea Marco; Borgogna Cinzia; Dell'Oste Valentina; Ferretti Massimo; Nicola Stefania; Cappellano Giuseppe; Carando Adriana; Leigheb Giorgio; Landolfo Santo; Dianzani Umberto; Gariglio Marisa
Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations.
The Journal of investigative dermatology 2008;128(3):732-5.
2006: Sorasio L; Ferrero G B; Garelli E; Brunello G; Martano C; Carando A; Belligni E; Dianzani I; Cirillo Silengo M
AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome.
European journal of medical genetics 2006;49(6):520-2.
2006: Campagnoli M F; Pucci A; Garelli E; Carando A; Defilippi C; Lala R; Ingrosso G; Dianzani I; Forni M; Ramenghi U
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family.
Journal of clinical pathology 2006;59(4):440-2.
2006: Campagnoli Maria Francesca; Garbarini Letizia; Quarello Paola; Garelli Emanuela; Carando Adriana; Baravalle Valentina; Doria Alessandra; Biava Alessandra; Chiocchetti Annalisa; Rosolen Angelo; Dufour Carlo; Dianzani Umberto; Ramenghi Ugo
The broad spectrum of autoimmune lymphoproliferative disease: molecular bases, clinical features and long-term follow-up in 31 patients.
Haematologica 2006;91(4):538-41.
2005: Chiocchetti Annalisa; Gibello Luisa; Carando Adriana; Aspesi Anna; Secco Paola; Garelli Emanuela; Loreni Fabrizio; Angelini Mara; Biava Alessandra; Dahl Niklas; Dianzani Umberto; Ramenghi Ugo; Santoro Claudio; Dianzani Irma
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein.
Haematologica 2005;90(11):1453-62.
2004: Campagnoli Maria Francesca; Garelli Emanuela; Quarello Paola; Carando Adriana; Varotto Stefania; Nobili Bruno; Longoni Daniela; Pecile Vanna; Zecca Marco; Dufour Carlo; Ramenghi Ugo; Dianzan Irma
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature.
Haematologica 2004;89(4):480-9.
2003: Dianzani I; Garelli E; Gustavsson P; Carando A; Gustafsson B; Dahl N; Annerén G
Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene.
Journal of medical genetics 2003;40(12):e133.
2000: Ramenghi U; Campagnoli M F; Garelli E; Carando A; Brusco A; Bagnara G P; Strippoli P; Izzi G C; Brandalise S; Riccardi R; Dianzani I
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population.
Blood cells, molecules & diseases 2000;26(5):417-22.

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Adriana Carando

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