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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
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June 5, 2022
Pain and agitation treatment in severe dementia patients: The need for Italian Mobilization-Observation-Behavior-Intensity-Dementia (I-MOBID2) pain scale translation, adaptation and validation with psychometric testing
D Scuteri, M Contrada, T Loria, et al.
Journal of Neurology
|
March 20, 2008
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism
Livia Bernardi, Carmine Tomaino, Maria Anfossi, et al.
Alzheimer Disease and Associated Disorders
|
December 11, 2008
The added value of neuropsychologic tests and structural imaging for the etiologic diagnosis of dementia in italian expert centers
Cristina Geroldi, Elisa Canu, Amalia C Bruni, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
August 24, 2000
Comparison of clinical and pathological phenotypes in two ethnically and geographically unrelated pedigrees segregating an equivalent presenilin 1 mutation
R Jorge, C Mangone, E Castano, et al.
Plos One
|
October 12, 2017
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia
Fernando Palluzzi, Raffaele Ferrari, Francesca Graziano, et al.
Neuroscience Letters
|
May 29, 2003
Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population
Manuela Di Natale, Maria Perri, Toshitaka Kawarai, et al.
Clinical Rheumatology
|
February 23, 2018
The safety of iloprost in systemic sclerosis in a real-life experience
S Bellando-Randone, C Bruni, G Lepri, et al.
Neurology
|
May 1, 1996
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family
A Quattrone, A Gambardella, F Bono, et al.
Neurology
|
September 15, 2004
A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene
G Rossi, G Giaccone, R Maletta, et al.
Reumatismo
|
March 8, 2021
Pulmonary arterial hypertension: guidelines and unmet clinical needs
D Giuggioli, C Bruni, F Cacciapaglia, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 199) with videos related to
Sort By:
Page
of 20
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
June 5, 2022
Pain and agitation treatment in severe dementia patients: The need for Italian Mobilization-Observation-Behavior-Intensity-Dementia (I-MOBID2) pain scale translation, adaptation and validation with psychometric testing
D Scuteri, M Contrada, T Loria, et al.
Journal of Neurology
|
March 20, 2008
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism
Livia Bernardi, Carmine Tomaino, Maria Anfossi, et al.
Alzheimer Disease and Associated Disorders
|
December 11, 2008
The added value of neuropsychologic tests and structural imaging for the etiologic diagnosis of dementia in italian expert centers
Cristina Geroldi, Elisa Canu, Amalia C Bruni, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
August 24, 2000
Comparison of clinical and pathological phenotypes in two ethnically and geographically unrelated pedigrees segregating an equivalent presenilin 1 mutation
R Jorge, C Mangone, E Castano, et al.
Plos One
|
October 12, 2017
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia
Fernando Palluzzi, Raffaele Ferrari, Francesca Graziano, et al.
Neuroscience Letters
|
May 29, 2003
Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population
Manuela Di Natale, Maria Perri, Toshitaka Kawarai, et al.
Clinical Rheumatology
|
February 23, 2018
The safety of iloprost in systemic sclerosis in a real-life experience
S Bellando-Randone, C Bruni, G Lepri, et al.
Neurology
|
May 1, 1996
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family
A Quattrone, A Gambardella, F Bono, et al.
Neurology
|
September 15, 2004
A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene
G Rossi, G Giaccone, R Maletta, et al.
Reumatismo
|
March 8, 2021
Pulmonary arterial hypertension: guidelines and unmet clinical needs
D Giuggioli, C Bruni, F Cacciapaglia, et al.
Page
of 20