‘A Budding Morrow in Midnight’: Facing Challenges and Embracing Opportunities during Lockdown at the Keats-Shelley House Museum in Rome

by Giuseppe Albano
Published 2021-06-01

‘A Budding Morrow in Midnight’: Facing Challenges and Embracing Opportunities during Lockdown at the Keats-Shelley House Museum in Rome

by Giuseppe Albano
Published 2021-06-01

¿Neumodesplazamiento vigente? Uso en hemorragia subretiniana y agujero macular traumático

by Gabriela Papa-Oliva, Giuseppe Albano-Quaglia, Ingrid Clemente, Adry Santamaría-Pacheco
Published 2015-07-01

Elevated FGF23 Levels in Mice Lacking the Thiazide-Sensitive NaCl cotransporter (NCC)

by Ganesh Pathare, Manuel Anderegg, Giuseppe Albano, Florian Lang, Daniel G. Fuster
Published 2018-02-01

Lack of NHE6 and Inhibition of NKCC1 Associated With Increased Permeability in Blood Labyrinth Barrier-Derived Endothelial Cell Layer

by Marijana Sekulic-Jablanovic, Jessica Paproth, Cinzia Sgambato, Giuseppe Albano, Daniel G. Fuster, Daniel Bodmer, Daniel Bodmer, Vesna Petkovic
Published 2022-04-01

Uterine Arteriovenous Fistula with Concomitant Pelvic Varicocele: Endovascular Embolization with Onyx-18®

by Francesco Giurazza, Fabio Corvino, Andrea Paladini, Antonio Borzelli, Domenico Scognamiglio, Giulia Frauenfelder, Giuseppe Albano, Fabio Sirimarco, Raffaella Niola
Published 2017-01-01

Artificial Intelligence and Forensic Genetics: Current Applications and Future Perspectives

by Francesco Sessa, Massimiliano Esposito, Giuseppe Cocimano, Sara Sablone, Michele Ahmed Antonio Karaboue, Mario Chisari, Davide Giuseppe Albano, Monica Salerno
Published 2024-03-01

Sodium-dependent phosphate transporters in osteoclast differentiation and function.

by Giuseppe Albano, Matthias Moor, Silvia Dolder, Mark Siegrist, Carsten A Wagner, Jürg Biber, Nati Hernando, Willy Hofstetter, Olivier Bonny, Daniel G Fuster
Published 2015-01-01

Loss of Sodium/Hydrogen Exchanger NHA2 Exacerbates Obesity- and Aging-Induced Glucose Intolerance in Mice.

by Christine Deisl, Manuel Anderegg, Giuseppe Albano, Benjamin P Lüscher, David Cerny, Rodrigo Soria, Elisa Bouillet, Stefano Rimoldi, Urs Scherrer, Daniel G Fuster
Published 2016-01-01

Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

by Jonai Pujol‐Giménez, Ghayda Mirzaa, Elizabeth E. Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth, James T. Bennett, Peter H. Byers, Sirisak Chanprasert, Jingheng Chen, Daniel Doherty, Andrew B. Folta, Madelyn A. Gillentine, Ian Glass, Anne Hing, Martha Horike‐Pyne, Kathleen A. Leppig, Azma Parhin, Jane Ranchalis, Wendy H. Raskind, Elisabeth A. Rosenthal, Ulrike Schwarze, Sam Sheppeard, Samuel Strohbehn, Virginia P. Sybert, Andrew Timms, Mark Wener, University of Washington Center for Mendelian Genomics (UW‐CMG)a, Undiagnosed Diseases Network (UDN), Michael J. Bamshad, Fuki M. Hisama, Gail P. Jarvik, Katrina M. Dipple, Matthias A. Hediger, Andrew B. Stergachis
Published 2023-06-01