Carlo Ferrarese

Increased tissue factor pathway inhibitor and homocysteine in Alzheimer's disease.

Diagnostic validity of optic disc and retinal nerve fiber layer evaluations in detecting structural changes after optic neuritis.

Clinical, neuropsychological, and morphometric correlates of apathy in Parkinson's disease.

Glutamate may be the soluble cerebrospinal fluid factor that induces calcium dysregulation in cultured astrocytes in HIV dementia.

Biological markers in Alzheimer disease.

Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome.

Altered glutamate uptake in peripheral tissues from Down syndrome patients.

Mitochondrial dysfunction due to mutant copper/zinc superoxide dismutase associated with amyotrophic lateral sclerosis is reversed by N-acetylcysteine.

Peripheral cytokine release in Alzheimer patients: correlation with disease severity.

The sinister side of Italian soccer.

Pharmacological manipulation of glutamate transport.

Glutamate transporters in platelets: EAAT1 decrease in aging and in Alzheimer's disease.

Peripheral markers of oxidative stress and excitotoxicity in neurodegenerative disorders: tools for diagnosis and therapy?

Oxidative stress impairs glutamate uptake in fibroblasts from patients with Alzheimer's disease.

Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.

An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy.

On scrapie interference and artificial prions.

Peripheral markers of glutamatergic dysfunction in neurological diseases: focus on ex vivo tools.

Increased plasma glutamate in stroke patients might be linked to altered platelet release and uptake.

Impairment of glutamate transport and increased vulnerability to oxidative stress in neuroblastoma SH-SY5Y cells expressing a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis.

Fibroblast glutamate transport in aging and in AD: correlations with disease severity.

Enhanced GM1 ganglioside catabolism in cultured fibroblasts from Alzheimer patients.

Vascular endothelial growth factor gene variability is associated with increased risk for AD.

Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.

Substrate-induced modulation of glutamate uptake in human platelets.

Increased susceptibility to plasma lipid peroxidation in Alzheimer disease patients.

Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis.

Assessing early to late stage dementia: the TSI and BANS-S scales in the nursing-home.

Is the inverse association between Alzheimer's disease and cancer the result of a different propensity to methylate DNA?

Oxidative stress in peripheral blood mononuclear cells from patients with Parkinson's disease: negative correlation with levodopa dosage.

Pathogenesis of retinal ganglion cell death in Leber hereditary optic neuropathy (LHON): possible involvement of mitochondria, light and glutamate.

Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.

Partial mitochondrial complex I inhibition induces oxidative damage and perturbs glutamate transport in primary retinal cultures. Relevance to Leber Hereditary Optic Neuropathy (LHON).

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.

Anatomical identification of active contacts in subthalamic deep brain stimulation.

Association between serum values of C-reactive protein and cytokine production in whole blood of patients with type 2 diabetes.

Young-onset CJD: age and disease phenotype in variant and sporadic forms.

Lack of evidence for oxidative stress in sporadic amyotrophic lateral sclerosis fibroblasts.

Enhanced folate binding of cultured fibroblasts from Alzheimer's disease patients.

Post-methionine load test: A more sensitive tool to reveal hyperhomocysteinemia in Alzheimer patients?

MELAS mitochondrial DNA mutation A3243G reduces glutamate transport in cybrids cell lines.

Rapidly cycling encephalopathy from an almost forgotten entity.

Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybrids.

Increased oxidative stress in lymphocytes from untreated Parkinson's disease patients.

Lymphomonocyte alpha-synuclein levels in aging and in Parkinson disease.

Lack of evidence for Borrelia burgdorferi seropositivity in Alzheimer disease.

Expression and distribution of 'high affinity' glutamate transporters GLT1, GLAST, EAAC1 and of GCPII in the rat peripheral nervous system.

Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study.

Platelets might mediate the increase of plasma glutamate in acute ischemic stroke: relevance for early neurological deterioration.

Increased soluble APPalpha, Abeta 1-42, and anti-Abeta 1-42 antibodies in plasma from down syndrome patients.

Neuroligand binding endophenotypes in blood cells distinguish two subsets of borderline personality disorder patients.

Higher than expected progranulin mutation rate in a case series of Italian FTLD patients.

Treatment of transiently symptomatic acute internal carotid artery occlusion: learning from the interventional field.

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease.

Sleepwalking in Italian operas: a window on popular and scientific knowledge on sleep disorders in the 19th century.

Alpha-synuclein nitration and autophagy response are induced in peripheral blood cells from patients with Parkinson disease.

Vesicular monoamine transporter 2 mRNA levels are reduced in platelets from patients with Parkinson's disease.

Arsenic eaters and altitude sickness: an epigenetic strategy for improving fitness in a hostile environment?

Cholinesterase inhibitor use is associated with increased plasma levels of anti-Aβ 1-42 antibodies in Alzheimer's disease patients.

Nonfibrillar Abeta 1-42 inhibits glutamate uptake and phosphorylates p38 in human fibroblasts.

Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration.

Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.

Mutual Information Optimization for Mass Spectra Data Alignment.

Generalized action myoclonus associated with escitalopram in a patient with mixed dementia.

Progressive supranuclear palsy-like phenotype caused by progranulin p.Thr272fs mutation.

Association analysis of PARP1 polymorphisms with Parkinson's disease.

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease.

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.

A panel of macroautophagy markers in lymphomonocytes of patients with amyotrophic lateral sclerosis.

Systemic thrombolysis in patients with acute ischemic stroke and Internal Carotid ARtery Occlusion: the ICARO study.

Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer disease.

Back to the ring: knocking-out headache.

Recessive loss-of-function mutation in the pacemaker HCN2 channel causing increased neuronal excitability in a patient with idiopathic generalized epilepsy.

Aβ42 production in brain capillary endothelial cells after oxygen and glucose deprivation.

Stroke-Unit and emergency medical service: a 48-month experience in northern Italy.

Valproate induces epigenetic modifications in lymphomonocytes from epileptic patients.

A case of spinal epidural haematoma during breath-hold diving.

Giuseppe Ferrario and the epidemiology of apoplexy during the 19th century.

Neurophysiological examination of dorsal sural nerve.

Plasma Anti-Amyloid-β Autoantibodies in All Alzheimer Disease Types.

Lombardia GENS: a collaborative registry for monogenic diseases associated with stroke.

[Disturbo dell'umore con sintomi psicotici e lesioni cutanee trascurate: lo strano caso della signora O].

Intravenous Thrombolysis for Acute Ischemic Stroke Associated to Extracranial Internal Carotid Artery Occlusion: The ICARO-2 Study.

Exploring limits of neuropsychological screening in ALS: The FAB problem.

Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson's disease.

Neuroleptic Equivalent Dose Differences and Behavioral and Psychological Symptoms of Dementia.