Andrea Calvo researcher (ORCID 0000-0002-5122-7243)
Calvo, Andrea
VIAF ID: 47666361 (Personal)
Permalink: http://viaf.org/viaf/47666361
Preferred Forms
- 100 0 _ ‡a Andrea Calvo ‡c researcher (ORCID 0000-0002-5122-7243)
- 100 1 _ ‡a Calvo, Andrea
- 100 1 _ ‡a Calvo, Andrea
4xx's: Alternate Name Forms (5)
5xx's: Related Names (1)
Works
Title | Sources |
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ALS clinical trials: Do enrolled patients accurately represent the ALS population? | |
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations | |
ALS mutant FUS proteins are recruited into stress granules in induced pluripotent stem cell-derived motoneurons | |
ALS patients and caregivers communication preferences and information seeking behaviour | |
Amyotrophic lateral sclerosis among the migrant population to Piemonte, northwestern Italy. | |
Amyotrophic lateral sclerosis/frontotemporal dementia with predominant manifestations of obsessive-compulsive disorder associated to GGGGCC expansion of the c9orf72 gene | |
Amyotrophic lateral sclerosis mimic syndrome due to a dorsal spinal cord neurofibroma | |
Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitor | |
artikull shkencor i botuar në vitin 2022 | |
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry | |
Caregiver burden and patients' perception of being a burden in ALS. | |
Caregiver time use in ALS | |
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. | |
Clinical features and outcomes of the flail arm and flail leg and pure lower motor neuron MND variants: a multicentre Italian study | |
Conjugal amyotrophic lateral sclerosis: suggestion for the implication of environmental factors | |
Dall'assistenza all'infanzia all'infermieristica pediatrica, 2018: | |
Erratum to: Brain hypermetabolism in amyotrophic lateral sclerosis: a FDG PET study in ALS of spinal and bulbar onset | |
Exome sequencing reveals VCP mutations as a cause of familial ALS | |
Exploring the phenotype of Italian patients with ALS with intermediate <i>ATXN2</i> polyQ repeats | |
Eye Tracking Impact on Quality-of-Life of ALS Patients | |
Genetic architecture of ALS in Sardinia | |
Genetic counselling in ALS: facts, uncertainties and clinical suggestions | |
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture | |
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. | |
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis | |
HFE p.H63D polymorphism does not influence ALS phenotype and survival | |
Idiopathic chronic inflammatory demyelinating polyneuropathy: an epidemiological study in Italy | |
Intrahemispheric and interhemispheric structural network abnormalities in PLS and ALS. | |
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene | |
The last months of life of people with amyotrophic lateral sclerosis in mechanical invasive ventilation: a qualitative study | |
A longitudinal study on quality of life and depression in ALS patient-caregiver couples | |
Lower serum lipid levels are related to respiratory impairment in patients with ALS. | |
Metabolic brain changes across different levels of cognitive impairment in ALS: a 18F-FDG-PET study | |
The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients | |
NADPH oxidase (NOX2) activity is a modifier of survival in ALS. | |
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis | |
Neurobehavioral dysfunction in ALS has a negative effect on outcome and use of PEG and NIV. | |
Neurobehavioral symptoms in ALS are negatively related to caregivers' burden and quality of life. | |
Neuroimaging in amyotrophic lateral sclerosis: insights into structural and functional changes | |
Neuropathology of olfactory ensheathing cell transplantation into the brain of two amyotrophic lateral sclerosis (ALS) patients. | |
A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year course | |
The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonisms | |
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels | |
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD | |
Percutaneous radiological gastrostomy: a safe and effective method of nutritional tube placement in advanced ALS. | |
Persistent idiopathic hypoglossal nerve palsy: A motor neuron disease-mimic syndrome? | |
Prevalence of SOD1 mutations in the Italian ALS population | |
Prospective epidemiological registers: a valuable tool for uncovering ALS pathogenesis | |
The rare G93D mutation causes a slowly progressing lower motor neuron disease. | |
Reduced cellular Ca(2+) availability enhances TDP-43 cleavage by apoptotic caspases. | |
Religiousness is positively associated with quality of life of ALS caregivers. | |
Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: Clinical and biological results from a prospective multicenter study | |
Resting state functional connectivity alterations in primary lateral sclerosis | |
The role of arterial blood gas analysis (ABG) in amyotrophic lateral sclerosis respiratory monitoring | |
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease | |
SOMAscan Proteomics Identifies Novel Plasma Proteins in Amyotrophic Lateral Sclerosis Patients | |
TDP-43 real-time quaking induced conversion reaction optimization and detection of seeding activity in CSF of amyotrophic lateral sclerosis and frontotemporal dementia patients | |
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation | |
Validation of the Italian version of self-administered ALSFRS-R scale | |
Validation of the revised classification of cognitive and behavioural impairment in ALS | |
Validity of hospital morbidity records for amyotrophic lateral sclerosis. A population-based study | |
Whole-blood global DNA methylation is increased in amyotrophic lateral sclerosis independently of age of onset |