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C Bruni

Showing results (121-130 of 199) with videos related to

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Neuroscience Letters|September 14, 1992
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) geneG Vaula, M Mortilla, R Tupler, et al.
Minerva Chirurgica|April 15, 1991
[The management of head trauma in a general surgery department. a contribution to an epidemiological analysis]G Grasso, A Lenzi, G C Bruni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17Elena Salvatore, Andrea Varrone, Valeria Sansone, et al.
Acta Endocrinologica|March 1, 1982
A case of ectopic ACTH syndrome: diagnostic difficulties caused by intermittent hormone secretionM O Thorner, W H Martin, G E Ragan, et al.
Journal of Geriatric Psychiatry and Neurology|January 1, 1994
A new Italian pedigree with early-onset Alzheimer's diseaseI Rainero, L Bergamini, A C Bruni, et al.
Revue Neurologique|December 17, 2004
[Familial fronto-temporal dementia with brain stem ubiquitin-positive neuronal inclusions]A C Bruni, T Kawarai, M G Spillantini, et al.
Neurobiology of Aging|April 17, 2013
First deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASILSilvia Bianchi, Maria Teresa Dotti, Gian Nicola Gallus, et al.
Ageing Research Reviews|September 13, 2023
Alzheimer's disease as a viral disease: Revisiting the infectious hypothesisFrancesco Bruno, Paolo Abondio, Rossella Bruno, et al.
Minerva Chirurgica|February 12, 1998
[Prosthetic repair of inguinal and crural hernias]D Balducci, V Postiglione, R Pancaldi, et al.
Aging Cell|April 15, 2016
NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's diseaseViviana Triaca, Valentina Sposato, Giulia Bolasco, et al.
Pageof 20

Showing results (121-130 of 199) with videos related to

Sort By:
Pageof 20
Neuroscience Letters|September 14, 1992
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) geneG Vaula, M Mortilla, R Tupler, et al.
Minerva Chirurgica|April 15, 1991
[The management of head trauma in a general surgery department. a contribution to an epidemiological analysis]G Grasso, A Lenzi, G C Bruni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2006
Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17Elena Salvatore, Andrea Varrone, Valeria Sansone, et al.
Acta Endocrinologica|March 1, 1982
A case of ectopic ACTH syndrome: diagnostic difficulties caused by intermittent hormone secretionM O Thorner, W H Martin, G E Ragan, et al.
Journal of Geriatric Psychiatry and Neurology|January 1, 1994
A new Italian pedigree with early-onset Alzheimer's diseaseI Rainero, L Bergamini, A C Bruni, et al.
Revue Neurologique|December 17, 2004
[Familial fronto-temporal dementia with brain stem ubiquitin-positive neuronal inclusions]A C Bruni, T Kawarai, M G Spillantini, et al.
Neurobiology of Aging|April 17, 2013
First deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASILSilvia Bianchi, Maria Teresa Dotti, Gian Nicola Gallus, et al.
Ageing Research Reviews|September 13, 2023
Alzheimer's disease as a viral disease: Revisiting the infectious hypothesisFrancesco Bruno, Paolo Abondio, Rossella Bruno, et al.
Minerva Chirurgica|February 12, 1998
[Prosthetic repair of inguinal and crural hernias]D Balducci, V Postiglione, R Pancaldi, et al.
Aging Cell|April 15, 2016
NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's diseaseViviana Triaca, Valentina Sposato, Giulia Bolasco, et al.
Pageof 20