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MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis

Cells (Basel, Switzerland), 2018-11, Vol.7 (11), p.219

2018

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KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants

Journal of molecular neuroscience, 2021-09, Vol.71 (9), p.1876-1883

2021

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Molecular Genetic Features of Cerebral Cavernous Malformations (CCM) Patients: An Overall View from Genes to Endothelial Cells

Cells (Basel, Switzerland), 2021-03, Vol.10 (3), p.704

2021

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A Novel Variant in Superoxide Dismutase 1 Gene ( p.V119M ) in Als Patients with Pure Lower Motor Neuron Presentation

Genes, 2021-09, Vol.12 (10), p.1544

2021

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Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1G93A Mice Predates Disease Onset and Is A Promising Therapeutic Target

iScience, 2020-05, Vol.23 (5), p.101087-101087, Article 101087

2020

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BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration

Brain sciences, 2022-05, Vol.12 (5), p.617

2022

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Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene

Human mutation, 2020-05, Vol.41 (5), p.1069-1071

2020

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Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort

Gene, 2015-09, Vol.568 (2), p.186-189

2015

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FUS mutations in sporadic amyotrophic lateral sclerosis

Neurobiology of aging, 2011-03, Vol.32 (3), p.550.e1-550.e4

2011

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Regulation of redox forms of plasma thiols by albumin in multiple sclerosis after fasting and methionine loading test

Amino acids, 2010-05, Vol.38 (5), p.1461-1471

2010

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A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Neuron (Cambridge, Mass.), 2011-10, Vol.72 (2), p.257-268

2011

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Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients

Neuromolecular medicine, 2016-12, Vol.18 (4), p.551-560

2016

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Genotype-phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-10, Vol.20 (7-8), p.611-614

2019

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Impaired intracortical transmission in G2019S leucine rich‐repeat kinase Parkinson patients

Movement disorders, 2017-05, Vol.32 (5), p.750-756

2017

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TBK1 is associated with ALS and ALS-FTD in Sardinian patients

Neurobiology of aging, 2016-07, Vol.43, p.180.e1-180.e5

2016

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Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

Neurobiology of aging, 2009-08, Vol.30 (8), p.1272-1275

2009

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Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT sub(5-8) Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC)

Molecular biotechnology, 2013-07, Vol.54 (3), p.874-879

2013

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Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT^sub 5â[euro]"8^ Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC)

Molecular biotechnology, 2013-07, Vol.54 (3), p.874

2013

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Corrigendum to “Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort” [GENE 568/2 (2015) 186–189]

Gene, 2016-04, Vol.581 (1), p.94-94

2016

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Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study

Journal of neurology, neurosurgery and psychiatry, 2015-08, Vol.86 (8), p.879-886

2015

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C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

Neurobiology of aging, 2012-08, Vol.33 (8), p.1848.e15-1848.e20

2012

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ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

Neurobiology of aging, 2015-10, Vol.36 (10), p.2906.e1-2906.e5

2015

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C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease

Neurological sciences, 2017, Vol.38 (1), p.207-208

2017

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MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis

KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants

Molecular Genetic Features of Cerebral Cavernous Malformations (CCM) Patients: An Overall View from Genes to Endothelial Cells

A Novel Variant in Superoxide Dismutase 1 Gene ( p.V119M ) in Als Patients with Pure Lower Motor Neuron Presentation

Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1G93A Mice Predates Disease Onset and Is A Promising Therapeutic Target

BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration

Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene

Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort

FUS mutations in sporadic amyotrophic lateral sclerosis

Regulation of redox forms of plasma thiols by albumin in multiple sclerosis after fasting and methionine loading test

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients

Genotype-phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Impaired intracortical transmission in G2019S leucine rich‐repeat kinase Parkinson patients

TBK1 is associated with ALS and ALS-FTD in Sardinian patients

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT sub(5-8) Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC)

Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT^sub 5â[euro]"8^ Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC)

Corrigendum to “Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort” [GENE 568/2 (2015) 186–189]

Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study

C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease

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