about
Clinical psychology and amyotrophic lateral sclerosis.Impaired expression of insulin-like growth factor-1 system in skeletal muscle of amyotrophic lateral sclerosis patients.Peptidylprolyl isomerase A governs TARDBP function and assembly in heterogeneous nuclear ribonucleoprotein complexes.Extrapyramidal and cognitive signs in amyotrophic lateral sclerosis: A population based cross-sectional study.Strictly monitored exercise programs reduce motor deterioration in ALS: preliminary results of a randomized controlled trial.Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.Valproate Treatment in an ALS Patient Carrying a c.194G>A Spastin Mutation and SMN2 Homozygous Deletion.Exploring motor and visual imagery in Amyotrophic Lateral Sclerosis.Grey matter damage in progressive multiple sclerosis versus amyotrophic lateral sclerosis: a voxel-based morphometry MRI study.Microstructural white matter correlates of emotion recognition impairment in Amyotrophic Lateral Sclerosis.BDNF Serum Levels with Respect to Multidimensional Assessment in Amyotrophic Lateral Sclerosis.How specific are the pontine MRI hyperintensities (the cross sign)?Brain MR Imaging in Patients with Lower Motor Neuron-Predominant Disease.Erratum to: Exploring motor and visual imagery in Amyotrophic Lateral Sclerosis.Emotional empathy in amyotrophic lateral sclerosis: a behavioural and voxel-based morphometry study.Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject.[Towards a multi-step informed consent: considerations and proposals for a good practice]Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotypeSerum irisin is upregulated in patients affected by amyotrophic lateral sclerosis and correlates with functional and metabolic statusPlasma amino acids patterns and age of onset of amyotrophic lateral sclerosisLack of relationship between the P413L chromogranin B variant and a SALS Italian cohortNo association of MTHFR c.677C>T variant with sporadic ALS in an Italian populationPhenotypic Heterogeneity in a SOD1 G93D Italian ALS Family: An Example of Human Model to Study a Complex DiseaseFree insulin-like growth factor (IGF)-1 and IGF-binding proteins-2 and -3 in serum and cerebrospinal fluid of amyotrophic lateral sclerosis patientsGastrostomy in amyotrophic lateral sclerosis: effects of non-invasive ventilationERRATUMThe prognostic value of spirometric tests in Amyotrophic Lateral Sclerosis patients
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