11. Gastrointestinal involvement in patients affected with 22q11.2 deletion syndrome. (March 2014) Authors: Giardino, Giuliana; Cirillo, Emilia; Maio, Filomena; Gallo, Vera; Esposito, Tiziana; Naddei, Roberta; Grasso, Fiorentino; Pignata, Claudio Journal: Scandinavian journal of gastroenterology Issue: Volume 49:Number 3(2014) Page Start: 274 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1. Issue 1 (2nd January 2021) Authors: Klionsky, Daniel J.; Abdel-Aziz, Amal Kamal; Abdelfatah, Sara; Abdellatif, Mahmoud; Abdoli, Asghar; Abel, Steffen; Abeliovich, Hagai; Abildgaard, Marie H.; Abudu, Yakubu Princely; Acevedo-Arozena, Abraham; Adamopoulos, Iannis E.; Adeli, Khosrow; Adolph, Timon E.; Adornetto, Annagrazia; Aflaki, El... Journal: Autophagy Issue: Volume 17:Issue 1(2021) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1. Issue 1 (2nd January 2021) Authors: Klionsky, Daniel J.; Abdel-Aziz, Amal Kamal; Abdelfatah, Sara; Abdellatif, Mahmoud; Abdoli, Asghar; Abel, Steffen; Abeliovich, Hagai; Abildgaard, Marie H.; Abudu, Yakubu Princely; Acevedo-Arozena, Abraham; Adamopoulos, Iannis E.; Adeli, Khosrow; Adolph, Timon E.; Adornetto, Annagrazia; Aflaki, El... Journal: Autophagy Issue: Volume 17:Issue 1(2021) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia. Issue 2 (5th June 2019) Authors: Nicita, Francesco; Nardella, Marta; Bellacchio, Emanuele; Alfieri, Paolo; Terrone, Gaetano; Piccini, Giorgia; Graziola, Federica; Pignata, Claudio; Capuano, Alessandro; Bertini, Enrico; Zanni, Ginevra Journal: Clinical genetics Issue: Volume 96:Issue 2(2019) Page Start: 169 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Impaired platelet activation in patients with hereditary deficiency of p47phox. (10th October 2016) Authors: Carnevale, Roberto; Loffredo, Lorenzo; Nocella, Cristina; Bartimoccia, Simona; Sanguigni, Valerio; Soresina, Annarosa; Plebani, Alessandro; Azzari, Chiara; Martire, Baldassarre; Pignata, Claudio; Violi, Francesco Journal: British journal of haematology Issue: Volume 180:Number 3(2018) Page Start: 454 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. In Ataxia-Telangiectasia, Oral Betamethasone Administration Ameliorates Lymphocytes Functionality through Modulation of the IL-7/IL-7Rα Axis Paralleling the Neurological Behavior: A Comparative Report of Two Cases. (17th February 2021) Authors: Prencipe, Rosaria; Cirillo, Emilia; Giardino, Giuliana; Gallo, Vera; Menotta, Michele; Magnani, Mauro; Barone, Maria Vittoria; Palamaro, Loredana; Scalia, Giulia; Del Vecchio, Luigi; Pignata, Claudio Journal: Immunological investigations Issue: Volume 50:Number 2/3(2021) Page Start: 295 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. In This Issue: FOX Genes and the Immune Response. (4th March 2014) Authors: Pignata, Claudio; Romano, Rosa Journal: International reviews of immunology Issue: Volume 33:Number 2(2014:Apr.) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. In This Issue: FOX Genes and the Immune Response. (4th March 2014) Authors: Pignata, Claudio; Romano, Rosa Journal: International reviews of immunology Issue: Volume 33:Number 2(2014:Apr.) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Insight into IKBKG/NEMO Locus: Report of New Mutations and Complex Genomic Rearrangements Leading to Incontinentia Pigmenti Disease. Issue 2 (12th December 2013) Authors: Conte, Matilde Immacolata; Pescatore, Alessandra; Paciolla, Mariateresa; Esposito, Elio; Miano, Maria Giuseppina; Lioi, Maria Brigida; McAleer, Maeve A.; Giardino, Giuliana; Pignata, Claudio; Irvine, Alan D.; Scheuerle, Angela E.; Royer, Ghislaine; Hadj‐Rabia, Smail; Bodemer, Christine; Bonnefont... Journal: Human mutation Issue: Volume 35:Issue 2(2014:Feb.) Page Start: 165 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. NADPH Oxidase Deficiency: A Multisystem Approach. (21st December 2017) Authors: Giardino, Giuliana; Cicalese, Maria Pia; Delmonte, Ottavia; Migliavacca, Maddalena; Palterer, Boaz; Loffredo, Lorenzo; Cirillo, Emilia; Gallo, Vera; Violi, Francesco; Pignata, Claudio Other Names: Crabtree Mark Academic Editor. Journal: Oxidative medicine and cellular longevity Issue: Volume 2017(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗