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ARCHIVES OF NEUROLOGY
Rivista
Codice:
E013975
ISSN:
0003-9942
Dati Generali
Dati Generali
Pubblicazioni (20)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A novel polymerase γ mutation in a family with ophthalmoplegia, neuropathy, and parkinsonism
Articolo
Abnormalities in the pattern of platelet amyloid precursor protein forms in patients with mild cognitive impairment and Alzheimer disease.
Articolo
Alzheimer disease and frontotemporal dementia.
Articolo
Amyloid precursor protein in platelets of patients with Alzheimer disease: effect of acetylcholinesterase inhibitor treatment.
Articolo
Antihypertensive medications influence the rate of conversion from mild cognitive impairment to Alzheimer disease.
Articolo
Association between tau H2 haplotype and age at onset in frontotemporal dementia
Articolo
Behavioral Disorders in Alzheimer disease: a Transcultural Perspective
Articolo
Behavioral disorders in Alzheimer disease: a transcultural perspective
Articolo
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase γ
Articolo
Depression is unrelated to conversion to dementia in patients with mild cognitive impairment.
Articolo
Differential level of platelet amyloid B precursor protein isoforms. An early marker for Alzheimer disease.
Articolo
Effect of transcranial magnetic stimulation on action naming in patients with Alzheimer disease
Articolo
Evidence of white matter changes on diffusion tensor imaging in frontotemporal dementia.
Articolo
Gadolinium-pentetic acid magnetic resonance imaging in patients with relapsing remitting multiple sclerosis.
Articolo
Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease.
Articolo
Immediate Anticoagulation With Heparin for First-Ever Ischemic Stroke in the Carotid. Artery Territories Observed Within 5 Hours of Onset.
Articolo
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene
Articolo
Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes
Articolo
Platelet amyloid precursor protein abnormalities in mild cognitive impairment predict conversion to dementia of Alzheimer type: a 2-year follow-up study.
Articolo
White matter changes in corticobasal degeneration syndrome and correlation with limb apraxia.
Articolo
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