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1
Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database
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Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database

Christina K. Lettieri ; Pamela Garcia-Filion ; Pooja Hingorani ; Larizza, Lidia ; Lidia Larizza

Journal of cancer epidemiology, 2014-12-01, Vol.2014 (2014), p.680126-5 [Rivista Peer Reviewed]

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Colorectal Cancer in Iran: Molecular Epidemiology and Screening Strategies
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Colorectal Cancer in Iran: Molecular Epidemiology and Screening Strategies

Roya Dolatkhah ; Mohammad Hossein Somi ; Mortaza Jabbarpour Bonyadi ; Iraj Asvadi Kermani ; Faris Farassati ; Saeed Dastgiri ; Larizza, Lidia ; Lidia Larizza

Journal of cancer epidemiology, 2015-12-01, Vol.2015, p.1-10 [Rivista Peer Reviewed]

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Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms
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Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms

Kloosterman, Wigard P ; Tavakoli-Yaraki, Masoumeh ; van Roosmalen, Markus J ; van Binsbergen, Ellen ; Renkens, Ivo ; Duran, Karen ; Ballarati, Lucia ; Vergult, Sarah ; Giardino, Daniela ; Hansson, Kerstin ; Ruivenkamp, Claudia A.L ; Jager, Myrthe ; van Haeringen, Arie ; Ippel, Elly F ; Haaf, Thomas ; Passarge, Eberhard ; Hochstenbach, Ron ; Menten, Björn ; Larizza, Lidia ; Guryev, Victor ; Poot, Martin ; Cuppen, Edwin

Cell reports (Cambridge), 2012-06, Vol.1 (6), p.648-655 [Rivista Peer Reviewed]

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Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes
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Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes

Cogliati, Francesca ; Giorgini, Valentina ; Masciadri, Maura ; Bonati, Maria Teresa ; Marchi, Margherita ; Cracco, Irene ; Gentilini, Davide ; Peron, Angela ; Savini, Miriam Nella ; Spaccini, Luigina ; Scelsa, Barbara ; Maitz, Silvia ; Veneselli, Edvige ; Prato, Giulia ; Pintaudi, Maria ; Moroni, Isabella ; Vignoli, Aglaia ; Larizza, Lidia ; Russo, Silvia

International journal of molecular sciences, 2019-07-24, Vol.20 (15), p.3621 [Rivista Peer Reviewed]

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5
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction
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Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction

Tabano, Silvia ; Colapietro, Patrizia ; Cetin, Irene ; Grati, Francesca R ; Zanutto, Susanna ; Mandò, Chiara ; Antonazzo, Patrizio ; Pileri, Paola ; Rossella, Franca ; Larizza, Lidia ; Sirchia, Silvia M ; Miozzo, Monica

Epigenetics, 2010-05-16, Vol.5 (4), p.313-324 [Rivista Peer Reviewed]

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6
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations
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Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations

Colombo, Elisa A ; Bazan, J Fernando ; Negri, Gloria ; Gervasini, Cristina ; Elcioglu, Nursel H ; Yucelten, Deniz ; Altunay, Ilknur ; Cetincelik, Umram ; Teti, Anna ; Del Fattore, Andrea ; Luciani, Matteo ; Sullivan, Spencer K ; Yan, Albert C ; Volpi, Ludovica ; Larizza, Lidia

Orphanet journal of rare diseases, 2012-01-23, Vol.7 (1), p.7-7 [Rivista Peer Reviewed]

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Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour
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Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour

Sparago, Angela ; Russo, Silvia ; Cerrato, Flavia ; Ferraiuolo, Serena ; Castorina, Pierangela ; Selicorni, Angelo ; Schwienbacher, Christine ; Negrini, Massimo ; Ferrero, Giovanni Battista ; Silengo, Margherita Cirillo ; Anichini, Cecilia ; Larizza, Lidia ; Riccio, Andrea

Human molecular genetics, 2007-02-01, Vol.16 (3), p.254-264 [Rivista Peer Reviewed]

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8
Nephrological findings and genotype–phenotype correlation in Beckwith–Wiedemann syndrome
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Nephrological findings and genotype–phenotype correlation in Beckwith–Wiedemann syndrome

Mussa, Alessandro ; Mussa, Alessandro ; Peruzzi, Licia ; Peruzzi, Licia ; Chiesa, Nicoletta ; Chiesa, Nicoletta ; De Crescenzo, Agostina ; De Crescenzo, Agostina ; Russo, Silvia ; Russo, Silvia ; Melis, Daniela ; Melis, Daniela ; Tarani, Luigi ; Tarani, Luigi ; Baldassarre, Giuseppina ; Baldassarre, Giuseppina ; Larizza, Lidia ; Larizza, Lidia ; Riccio, Andrea ; Riccio, Andrea ; Silengo, Margherita ; Silengo, Margherita ; Ferrero, Giovanni Battista ; Ferrero, Giovanni Battista

Pediatric Nephrology, 2012-03, Vol.27 (3), p.397-406 [Rivista Peer Reviewed]

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9
Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features
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Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features

Cirello, Valentina ; Giorgini, Valentina ; Castronovo, Chiara ; Marelli, Susan ; Mainini, Ester ; Sironi, Alessandra ; Recalcati, Maria Paola ; Pessina, Marco ; Giardino, Daniela ; Larizza, Lidia ; Persani, Luca ; Finelli, Palma ; Russo, Silvia ; Fugazzola, Laura

Frontiers in genetics, 2018-11-30, Vol.9, p.600 [Rivista Peer Reviewed]

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10
Rothmund-Thomson syndrome
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Rothmund-Thomson syndrome

Larizza, Lidia ; Roversi, Gaia ; Volpi, Ludovica

Orphanet journal of rare diseases, 2010-01-29, Vol.5 (1), p.2-2 [Rivista Peer Reviewed]

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