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ANNALS OF NEUROLOGY
Rivista
Codice:
E009444
ISSN:
0364-5134
Dati Generali
Dati Generali
Pubblicazioni (57)
Pulisci
Ordina Pubblicazioni:
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A molecular classification of Joubert syndrome
Abstract
A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy
Articolo
A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy.
Articolo
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders
Articolo
Adoptive Transfer of JC Virus-Specific T Lymphocytes for the Treatment of Progressive Multifocal Leukoencephalopathy
Articolo
Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load
Articolo
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome
Articolo
Classification Accuracy of Transcranial Magnetic Stimulation for the Diagnosis of Neurodegenerative Dementias
Articolo
Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: An F-18-dopa PET study
Articolo
Clinical correlates of apolipoprotein E in Alzheimer's disease.
Articolo
DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial cervical or upper limb onset
Articolo
Deep gray matter volume loss drives disability worsening in multiple sclerosis
Articolo
Distinguishing the four genetic causes of Jouberts syndrome-related disorders
Articolo
Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38
Articolo
Dopa-responsive dystonia: A clinical and molecular genetic study
Articolo
Familiar perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment
Articolo
Gene dose of the epsilon 4 allele of apolipoprotein E and disease progression in sporadic late-onset Alzheimer's disease.
Articolo
Heterozygous NOTCH1 Variants Cause CNS Immune Activation and Microangiopathy
Articolo
High endogenous cannabinoid levels in the cerebrospinal fluid of untreated Parkinson's disease patients
Articolo
High‐Dose Pulse Glucocorticoid Treatment Prevents White Matter Spinal Cord Pseudoatrophy in Newly Diagnosed Multiple Sclerosis
Articolo
Independent and Joint Effects of the MAPT and SNCA Genes in Parkinson Disease
Articolo
Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly.
Articolo
Long-term survival in amyotrophic lateral sclerosis: a population-based study
Articolo
Longitudinal spinal cord atrophy in multiple sclerosis using the generalized boundary shift integral
Articolo
Low myo-inositol indicating astrocytic damage in a case series of neuromyelitis optica
Articolo
Metallothioneins are neuroprotective agents in lysosomal storage disorders
Articolo
Migraine and Cryptogenic Ischemic Stroke
Articolo
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy
Articolo
Mitochondrial oxidative phosphorylation defects in Parkinson Disease
Articolo
Mitochondrial oxidative phosphorylation defects in Parkinson's disease
Articolo
Multiple SclerosisIs Rare in Epstein–Barr Virus–Seronegative Children withCentral Nervous SystemInflammatory Demyelination
Articolo
Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine
Articolo
Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34
Articolo
Ocular oscillations induced by shifts of the direction and depth of visual fixation
Articolo
Olfactory Neuron Prokineticin-2 as a Potential Target in Parkinson's Disease
Articolo
PARK6-linked parkinsonism occurs in several European families
Articolo
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation
Articolo
PINK1 mutations are associated with sporadic early-onset parkinsonism
Articolo
Pallidal stimulation improves pantothenate kinase-associated neurodegeneration
Articolo
Pathological and immunological observations on tropical spastic paraparesis in patients from Jamaica
Articolo
Physical activity and amyotrophic lateral sclerosis: a European population-based case-control study
Articolo
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors
Articolo
Presynaptic Dopaminergic Imaging Characterizes Patients with REM Sleep Behavior Disorder Due to Synucleinopathy
Articolo
Reply to "Spinal Cord Atrophy Is a Preclinical Marker of Progressive MS"
Articolo
Risk Factors for Phenoconversion in Rapid Eye Movement Sleep Behavior Disorder
Articolo
Risk factors for neurodegeneration in idiopathic rapid eye movement sleep behavior disorder: A multicenter study
Articolo
Saccadic palsy after cardiac surgery: characteristics and pathogenesis.
Articolo
Serotonin transporter in Parkinson's disease: A meta-analysis of positron emission tomography studies
Articolo
Silent progression in disease activity-free relapsing multiple sclerosis
Articolo
Spinal Cord Atrophy Predicts Progressive Disease in Relapsing Multiple Sclerosis
Articolo
Spinal cord gray matter atrophy correlates with multiple sclerosis disability
Articolo
Striatal spiny neurons and cholinergic interneurons express differential ionotropic glutamatergic responses and vulnerability: implications for ischemia and Huntington's disease
Articolo
Structural Variants at the LMNB1 Locus: Deciphering Pathomechanisms in Autosomal Dominant Adult-Onset Demyelinating Leukodystrophy
Articolo
Subthalamic infusion of an NMDA antagonist prevents basal ganglia metabolic changes and nigral degeneration in a rodent model of Parkinson's disease
Articolo
Syndromic parkinsonism and dementia associated with OPA1 missense mutations
Articolo
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy
Articolo
Using global team science to identify genetic parkinson's disease worldwide
Articolo
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