1. Absence of acquired copy number neutral loss of heterozygosity (CN‐LOH) of chromosome 7 in a series of 10 patients with Shwachman–Diamond syndrome. (1st February 2014) Authors: Nacci, Lucia; Danesino, Cesare; Sainati, Laura; Longoni, Daniela; Poli, Furio; Cipolli, Marco; Perobelli, Sandra; Nicolis, Elena; Cannioto, Zemira; Morini, Jacopo; Valli, Roberto; Pasquali, Francesco; Minelli, Antonella Journal: British journal of haematology Issue: Volume 165:Number 4(2014:May) Page Start: 573 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comparative genomic hybridization on microarray (a‐CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature. Issue 12 (10th September 2015) Authors: Valli, Roberto; De Bernardi, Francesca; Frattini, Annalisa; Volpi, Luca; Bignami, Maurizio; Facchetti, Fabio; Pasquali, Francesco; Castelnuovo, Paolo; Maserati, Emanuela Journal: Genes, chromosomes & cancer Issue: Volume 54:Issue 12(2015:Dec.) Page Start: 771 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cytogenetic Monitoring in Shwachman-Diamond Syndrome. Issue 4 (May 2015) Authors: Pressato, Barbara; Valli, Roberto; Marletta, Cristina; Mare, Lydia; Montalbano, Giuseppe; Curto, Francesco Lo; Pasquali, Francesco; Maserati, Emanuela Journal: Journal of pediatric hematology/oncology Issue: Volume 37:Issue 4(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning. Issue 4 (May 2015) Authors: Pressato, Barbara; Valli, Roberto; Marletta, Cristina; Mare, Lydia; Montalbano, Giuseppe; Curto, Francesco Lo; Pasquali, Francesco; Maserati, Emanuela Journal: Journal of pediatric hematology/oncology Issue: Volume 37:Issue 4(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia. (31st December 2021) Authors: Azzolini, Claudio; Donati, Simone; Micheloni, Giovanni; Moretti, Vittoria; Valli, Roberto; Acquati, Francesco; Costantino, Lucy; Ferrara, Fulvio; Borroni, Davide; Premi, Elias; Testa, Francesco; Simonelli, Francesca; Porta, Giovanni Other Names: Thomas Biju B. Academic Editor. Journal: Journal of ophthalmology Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel recurrent chromosome anomalies in Shwachman–Diamond syndrome. Issue 8 (28th January 2017) Authors: Valli, Roberto; De Paoli, Elena; Nacci, Lucia; Frattini, Annalisa; Pasquali, Francesco; Maserati, Emanuela Journal: Pediatric blood & cancer Issue: Volume 64:Issue 8(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Parental origin of the deletion del(20q) in Shwachman‐Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene. Issue 1 (21st September 2016) Authors: Nacci, Lucia; Valli, Roberto; Maria Pinto, Rita; Zecca, Marco; Cipolli, Marco; Morini, Jacopo; Cesaro, Simone; Boveri, Emanuela; Rosti, Vittorio; Corti, Paola; Ambroni, Maura; Pasquali, Francesco; Danesino, Cesare; Maserati, Emanuela; Minelli, Antonella Journal: Genes, chromosomes & cancer Issue: Volume 56:Issue 1(2017:Jan.) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis. (3rd October 2017) Authors: Valli, Roberto; Frattini, Annalisa; Minelli, Antonella Journal: Expert opinion on orphan drugs Issue: Volume 5:Number 10(2017:Oct.) Page Start: 753 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Shwachman‐Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability. (26th December 2018) Authors: Valli, Roberto; Minelli, Antonella; Galbiati, Marta; D'Amico, Giovanna; Frattini, Annalisa; Montalbano, Giuseppe; Khan, Abdul W.; Porta, Giovanni; Millefanti, Giorgia; Olivieri, Carla; Cipolli, Marco; Cesaro, Simone; Pasquali, Francesco; Danesino, Cesare; Cazzaniga, Gianni; Maserati, Emanuela Journal: British journal of haematology Issue: Volume 184:Number 6(2019) Page Start: 974 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family. Issue 1 (1st November 2021) Authors: Micheloni, Giovanni; Carnovali, Marta; Millefanti, Giorgia; Rizzetto, Manuel; Moretti, Vittoria; Montalbano, Giuseppe; Acquati, Francesco; Giaroni, Cristina; Valli, Roberto; Costantino, Lucy; Ferrara, Fulvio; Banfi, Giuseppe; Mariotti, Massimo; Porta, Giovanni Journal: International journal of experimental pathology Issue: Volume 103:Issue 1(2022) Page Start: 13 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗