A. Conte

M. Sabatelli, A. Conte, M. Zollino, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Natural history of young-adult amyotrophic lateral sclerosis

P. Tonali, M. Lo Monaco, M. Sabatelli, 2008, Neurology.

A new single‐nucleotide deletion of PMP22 in an HNPP family without recurrent palsies

P. Tonali, M. Sabatelli, A. Conte, 2008, Muscle & nerve.

Randomised controlled trial of methotrexate for chronic inflammatory demyelinating polyradiculoneuropathy (RMC trial): a pilot, multicentre study

M. Lucchetta, D. Pareyson, A. Schenone, 2009, The Lancet Neurology.

SEIPIN S90L Mutation in an Italian family with CMT2/dHMN and pyramidal signs

M. Sabatelli, A. Conte, M. Ferrarini, 2010, Muscle & nerve.

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Sonja W. Scholz, Hannah A. Pliner, Janel O. Johnson, 2021, JAMA neurology.

A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype

P. Tonali, G. Tasca, M. Sabatelli, 2010, Journal of the Neurological Sciences.

Thr124Met myelin protein zero mutation mimicking motor neuron disease

G. Tasca, M. Sabatelli, A. Conte, 2021, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients

A. Vescovi, L. De Gioia, S. Martino, 2022, Antioxidants.

P525L FUS mutation is consistently associated with a severe form of juvenile Amyotrophic Lateral Sclerosis

S. Servidei, M. Sabatelli, A. Conte, 2012, Neuromuscular Disorders.

D11Y SOD1 mutation and benign ALS: A consistent genotype-phenotype correlation

M. Sabatelli, A. Conte, M. Zollino, 2011, Journal of the Neurological Sciences.

Psychological Profile of the Amyotrophic Lateral Sclerosis (ALS) Patients’: A Descriptive Pilot Study base on the Cognitive Systemic Approach

D. Marchione, A. Conte, G. Bisogni, 2019 .

Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients

J. Mandrioli, M. Sabatelli, A. Conte, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

SOD1 p.D12Y variant is associated with amyotrophic lateral sclerosis/distal myopathy spectrum

G. Tasca, P. Mandich, B. Udd, 2020, European journal of neurology.

SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis

P. Tonali, M. Dileone, M. Sabatelli, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation

P. Rossini, G. Neri, M. Sabatelli, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Sural nerve pathology in ALS patients: a single-centre experience

M. Sabatelli, A. Conte, M. Luigetti, 2012, Neurological Sciences.

NEUROLOGIC IMPROVEMENT AFTER PERIPHERAL BLOOD STEM CELL TRANSPLANTATION IN POEMS

P. Chiusolo, M. Sabatelli, A. Conte, 2009, Neurology.

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

A. Chiò, G. Mora, G. Logroscino, 2018, European journal of neurology.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene in and for Therapeutic

Timothy A. Miller, Denis C. Bauer, Shankaracharya, 2018 .

Cardiovascular diseases may play a negative role in the prognosis of ALS

Sonia, Messina, G. Mora, 2018 .

Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy

M. Sabatelli, A. Conte, L. Laurenti, 2012, Journal of the Neurological Sciences.

Light chain deposition in peripheral nerve as a cause of mononeuritis multiplex in Waldenström's macroglobulinaemia

P. Tonali, P. Profice, M. Sabatelli, 2010, Journal of the Neurological Sciences.

A novel L67P SOD1 mutation in an Italian ALS patient

M. Sabatelli, A. Conte, M. Zollino, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Skin Changes in POEMS Syndrome

M. Sabatelli, A. Conte, M. Luigetti, 2014, European Neurology.

Early diagnosis followed by front-line autologous peripheral blood stem cell transplantation for patients affected by POEMS syndrome.

P. Chiusolo, G. Leone, M. Sabatelli, 2008, Leukemia research.

Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients

C. Bernardini, F. Michetti, G. Logroscino, 2017, Scientific Reports.

High-Throughput Genetic Testing in ALS: The Challenging Path of Variant Classification Considering the ACMG Guidelines

M. Sabatelli, A. Conte, M. Zollino, 2020, Genes.

Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis.

P. Rossini, M. Mirabella, M. Sabatelli, 2013, Human molecular genetics.

FUS mutations in sporadic amyotrophic lateral sclerosis

D. Stephan, M. Cookson, T. Dunckley, 2011, Neurobiology of Aging.

Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis.

F. Eusebi, C. Limatola, A. Al-Chalabi, 2009, Human molecular genetics.

Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis.

D. Colavito, E. Del Giudice, M. Sabatelli, 2021, Human molecular genetics.

G. Tasca, M. Sabatelli, A. Conte, 2016, Brain pathology.

Matrin 3 variants are frequent in Italian ALS patients

G. Tasca, M. Sabatelli, A. Conte, 2017, Neurobiology of Aging.

Triple A syndrome: A novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency

A. Pizzuti, H. Houlden, I. Bottillo, 2010, Journal of the Neurological Sciences.

Sural nerve biopsy in peripheral neuropathies: 30-year experience from a single center

P. Rossini, M. Sabatelli, A. Conte, 2019, Neurological Sciences.

A novel GJB1 mutation in an Italian patient with Charcot–Marie–Tooth disease and pyramidal signs

F. Ranieri, M. Sabatelli, A. Conte, 2011, Muscle & nerve.

Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation

M. Sabatelli, A. Conte, G. Fabrizi, 2011, Journal of the Neurological Sciences.

M. Lo Monaco, G. Merlini, M. Sabatelli, 2013, Neurological Sciences.

Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathy

G. Tasca, L. Lauriola, M. Sabatelli, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.

A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia

M. Papacci, G. Tasca, G. Silvestri, 2010, Clinical Neurology and Neurosurgery.

pSTAT1, pSTAT3, and T‐bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy

P. Tonali, M. Sabatelli, A. Conte, 2009, Journal of the peripheral nervous system : JPNS.

Pathological Findings in Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Single-Center Experience

M. Sabatelli, A. Conte, M. Luigetti, 2020, Brain sciences.

Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis

D. Marchione, E. Del Giudice, A. Leon, 2023, European journal of neurology.

SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant

M. Sabatelli, A. Conte, M. Zollino, 2011, Neurobiology of Aging.

Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS

L. Pozzi, M. Sabatelli, A. Conte, 2019, Neurobiology of Aging.

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

F. Marrosu, A. Chiò, G. Mora, 2012, Brain : a journal of neurology.

Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis

V. Di Lazzaro, P. Tonali, M. Dileone, 2009, Neurological Sciences.

Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double‐blind, placebo‐controlled trial

S. Paganoni, E. Beghi, G. Logroscino, 2022, European journal of neurology.

ATXN2 polyQ intermediate repeats are a modifier of ALS survival

A. Chiò, G. Mora, A. Calvo, 2015, Neurology.

Posterior ischaemic myelopathy associated with cocaine abuse

M. Sabatelli, A. Conte, A. Cianfoni, 2010, Internal medicine journal.

Clinical features and outcomes of the flail arm and flail leg and pure lower motor neuron MND variants: a multicentre Italian study

L. Pozzi, M. Filippi, A. Chiò, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort

A. Chiò, G. Mora, G. Logroscino, 2017, Journal of Neurology.

Clinical features and outcomes of the flail arm and flail leg and pure lower motor neuron MND variants: a multicenter Italian study

Messina, Lunetta, L. Pozzi, 2020 .

Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else?

T. Tartaglione, M. Sabatelli, A. Conte, 2011, Journal of Neurology.

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

Hannah A. Pliner, A. Mulas, F. Marrosu, 2016, Neurobiology of Aging.

Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's disease

P. Tonali, M. Sabatelli, A. Conte, 2002, Neuromuscular Disorders.

Neuropathy with predominant small fiber involvement associated with abnormal anti-MAG titer.

P. Tonali, M. Sabatelli, A. Conte, 2010, Internal medicine.

Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant.

M. Sabatelli, A. Conte, D. Orteschi, 2021, Stem cell research.

Peripheral neuropathy and 46XY gonadal dysgenesis: Confirmation of a heterogeneous entity

S. Corsello, M. Sabatelli, A. Conte, 2012, Clinical Neurology and Neurosurgery.

Clinical and genetic heterogeneity of amyotrophic lateral sclerosis

M. Sabatelli, A. Conte, M. Zollino, 2013, Clinical genetics.

D11Y SOD1 mutation and benign ALS: A consistent genotype-phenotype correlation

A. Conte, M. Luigetti, G. Bisogni, 2011, Journal of the Neurological Sciences.

Characterization of SOD1-DT, a Divergent Long Non-Coding RNA in the Locus of the SOD1 Human Gene

C. Bernardini, C. Sette, M. Sabatelli, 2023, Cells.

Primary multifocal lymphoma of peripheral nervous system: Case report and review of the literature

S. Hohaus, G. Granata, L. Lauriola, 2014, Muscle & nerve.

pSTAT1, pSTAT3, and T‐bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy

P. Tonali, M. Sabatelli, A. Conte, 2009, Journal of the peripheral nervous system : JPNS.

Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: A single-centre experience

P. Rossini, M. Sabatelli, A. Conte, 2014, Journal of the Neurological Sciences.

A new single‐nucleotide deletion of PMP22 in an HNPP family without recurrent palsies

P. Tonali, M. Sabatelli, A. Conte, 2008, Muscle & nerve.

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Hannah A. Pliner, John D. Eicher, Janel O. Johnson, 2021, JAMA Neurology.

Clinical, electrophysiological and pathological findings in a patient with Charcot–Marie–Tooth disease 4D caused by the NDRG1 Lom mutation

E. Mercuri, F. Taroni, M. Sabatelli, 2014, Journal of Neurological Sciences.