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Clinical Nutrition ESPEN
|
November 5, 2018
Non-Celiac Gluten Sensitivity in patients with severe abdominal pain and bloating: The accuracy of ALCAT 5
Michele Di Stefano, Eugenia Vittoria Pesatori, Giulia Francesca Manfredi, et al.
Journal of Neuropathology and Experimental Neurology
|
February 7, 2007
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease
Giuseppe Di Fede, Giorgio Giaccone, Lucia Limido, et al.
Neurobiology of Disease
|
January 22, 2016
The new β amyloid-derived peptide Aβ1-6A2V-TAT(D) prevents Aβ oligomer formation and protects transgenic C. elegans from Aβ toxicity
Luisa Diomede, Margherita Romeo, Alfredo Cagnotto, et al.
Frontiers in Aging Neuroscience
|
March 11, 2021
Machine Learning Profiling of Alzheimer's Disease Patients Based on Current Cerebrospinal Fluid Markers and Iron Content in Biofluids
Eleonora Ficiarà, Silvia Boschi, Shoeb Ansari, et al.
Alzheimer Disease and Associated Disorders
|
March 16, 2022
Psychological Impact of Predictive Genetic Testing for Inherited Alzheimer Disease and Frontotemporal Dementia: The IT-DIAfN Protocol
Samantha Galluzzi, Anna Mega, Giuseppe Di Fede, et al.
Brain : a Journal of Neurology
|
March 8, 2023
Defining the phenotypic spectrum of sporadic Creutzfeldt-Jakob disease MV2K: the kuru plaque type
Simone Baiardi, Angela Mammana, Sofia Dellavalle, et al.
Neurobiology of Disease
|
January 2, 2016
The cell-permeable Aβ1-6A2VTAT(D) peptide reverts synaptopathy induced by Aβ1-42wt
Sara Cimini, Alessandra Sclip, Simona Mancini, et al.
Journal of the Neurological Sciences
|
December 21, 2010
Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu
Ettore Salsano, Roberto Fancellu, Giuseppe Di Fede, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 23, 2011
A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration
Cinzia Coppola, Giacomina Rossi, Anna Maria Barbarulo, et al.
Journal of Neuropathology and Experimental Neurology
|
October 22, 2002
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients
Mariarosa A B Melone, Giuseppe Di Fede, Gianfranco Peluso, et al.
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of 9
Search research articles
Search
Showing results (21-30 of 84) with videos related to
Sort By:
Page
of 9
Clinical Nutrition ESPEN
|
November 5, 2018
Non-Celiac Gluten Sensitivity in patients with severe abdominal pain and bloating: The accuracy of ALCAT 5
Michele Di Stefano, Eugenia Vittoria Pesatori, Giulia Francesca Manfredi, et al.
Journal of Neuropathology and Experimental Neurology
|
February 7, 2007
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease
Giuseppe Di Fede, Giorgio Giaccone, Lucia Limido, et al.
Neurobiology of Disease
|
January 22, 2016
The new β amyloid-derived peptide Aβ1-6A2V-TAT(D) prevents Aβ oligomer formation and protects transgenic C. elegans from Aβ toxicity
Luisa Diomede, Margherita Romeo, Alfredo Cagnotto, et al.
Frontiers in Aging Neuroscience
|
March 11, 2021
Machine Learning Profiling of Alzheimer's Disease Patients Based on Current Cerebrospinal Fluid Markers and Iron Content in Biofluids
Eleonora Ficiarà, Silvia Boschi, Shoeb Ansari, et al.
Alzheimer Disease and Associated Disorders
|
March 16, 2022
Psychological Impact of Predictive Genetic Testing for Inherited Alzheimer Disease and Frontotemporal Dementia: The IT-DIAfN Protocol
Samantha Galluzzi, Anna Mega, Giuseppe Di Fede, et al.
Brain : a Journal of Neurology
|
March 8, 2023
Defining the phenotypic spectrum of sporadic Creutzfeldt-Jakob disease MV2K: the kuru plaque type
Simone Baiardi, Angela Mammana, Sofia Dellavalle, et al.
Neurobiology of Disease
|
January 2, 2016
The cell-permeable Aβ1-6A2VTAT(D) peptide reverts synaptopathy induced by Aβ1-42wt
Sara Cimini, Alessandra Sclip, Simona Mancini, et al.
Journal of the Neurological Sciences
|
December 21, 2010
Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu
Ettore Salsano, Roberto Fancellu, Giuseppe Di Fede, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 23, 2011
A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration
Cinzia Coppola, Giacomina Rossi, Anna Maria Barbarulo, et al.
Journal of Neuropathology and Experimental Neurology
|
October 22, 2002
Abnormal accumulation of tTGase products in muscle and erythrocytes of chorea-acanthocytosis patients
Mariarosa A B Melone, Giuseppe Di Fede, Gianfranco Peluso, et al.
Page
of 9