Showing results (641-650 of 694) with videos related to

Sort By:
Pageof 70
Neurobiology of Disease|June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitabilityMattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, et al.
Frontiers in Molecular Neuroscience|August 22, 2018
A Loss-of-Function <i>HCN4</i> Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal ExcitabilityGiulia Campostrini, Jacopo C DiFrancesco, Barbara Castellotti, et al.
British Journal of Haematology|May 22, 2008
Biological and clinical risk factors of chronic lymphocytic leukaemia transformation to Richter syndromeDavide Rossi, Michaela Cerri, Daniela Capello, et al.
American Journal of Human Genetics|May 22, 2012
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosageKatherine R Smith, John Damiano, Silvana Franceschetti, et al.
Annals of Neurology|October 23, 2009
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failureL M Dibbens, R Michelucci, A Gambardella, et al.
Blood|August 29, 2012
Final results of a multicenter trial addressing role of CSF flow cytometric analysis in NHL patients at high risk for CNS disseminationGiulia Benevolo, Alessandra Stacchini, Michele Spina, et al.
Clinical Neurophysiology Practice|November 19, 2024
A Reappraisal on cortical myoclonus and brief Remarks on myoclonus of different OriginsLaura Canafoglia, Stefano Meletti, Francesca Bisulli, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 15, 2010
Phase II trial of short-course R-CHOP followed by 90Y-ibritumomab tiuxetan in previously untreated high-risk elderly diffuse large B-cell lymphoma patientsPier Luigi Zinzani, Giuseppe Rossi, Silvia Franceschetti, et al.
British Journal of Haematology|November 30, 2010
Immunogenetics features and genomic lesions in splenic marginal zone lymphomaAndrea Rinaldi, Francesco Forconi, Luca Arcaini, et al.
Epilepsia|October 2, 2014
Mild Lafora disease: clinical, neurophysiologic, and genetic findingsEdoardo Ferlazzo, Laura Canafoglia, Roberto Michelucci, et al.
Pageof 70