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Update upon efficacy and safety of etanercept for the treatment of spondyloarthritis and juvenile idiopathic arthritis

Modern rheumatology, 2018-05, Vol.28 (3), p.417-431

2018

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Current Views on Diagnostic Approach and Treatment of Lymphedema

The American journal of medicine, 2012-02, Vol.125 (2), p.134-140

2012

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HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients

Journal of the peripheral nervous system, 2011-12, Vol.16 (4), p.287-294

2011

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Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise"

Orphanet journal of rare diseases, 2018-10, Vol.13 (1), p.177-177, Article 177

2018

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Severe Neuropathy After Diphtheria-Tetanus-Pertussis Vaccination in a Child Carrying a Novel Frame-Shift Mutation in the Small Heat-Shock Protein 27 Gene

Journal of child neurology, 2010-01, Vol.25 (1), p.107-109

2010

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Endothelial dysfunction in rheumatic autoimmune diseases

Atherosclerosis, 2012-10, Vol.224 (2), p.309-317

2012

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Gap junction beta 1 ( ) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease

Journal of human genetics, 2008-06, Vol.53 (6), p.529-533

2008

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TNF-α Gene Polymorphisms: Association with Disease Susceptibility and Response to Anti-TNF-α Treatment in Psoriatic Arthritis

Journal of investigative dermatology, 2014-10, Vol.134 (10), p.2503-2509

2014

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Genetic factors and systemic sclerosis

Autoimmunity reviews, 2016-05, Vol.15 (5), p.427-432

2016

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Nocturia: An Uncommon Presentation of Lower-Limb Lymphedema

The American journal of medicine, 2010-03, Vol.123 (3), p.e3-e4

2010

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Update upon efficacy and safety of TNF-α inhibitors

Expert opinion on drug safety, 2012-01, Vol.11 (1), p.1-5

2012

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TNF-[alpha] Gene Polymorphisms: Association with Disease Susceptibility and Response to Anti-TNF-[alpha] Treatment in Psoriatic Arthritis

Journal of investigative dermatology, 2014-10, Vol.134 (10), p.2503

2014

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A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot–Marie–Tooth disease

Journal of the neurological sciences, 2014-08, Vol.343 (1), p.183-186

2014

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Pharmacogenetics and Future Therapeutic Scenarios: What Affects the Prediction of Response to Treatment with Etanercept?

Drug development research, 2014-11, Vol.75 (S1), p.S7-S10

2014

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Two novel cases of compound heterozygous mutations in mitofusin2: finding out the inheritance

Neuromuscular disorders : NMD, 2017-04, Vol.27 (4), p.377-381

2017

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Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: Findings in an Italian cohort of patients with Parkinsonian syndromes and relevance for genetic counselling

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2013-09, Vol.14 (5-6), p.479-480

2013

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Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies

European journal of human genetics : EJHG, 2009-09, Vol.17 (9), p.1129-1134

2009

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1993–2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa

Molecular genetics & genomic medicine, 2017-09, Vol.5 (5), p.473-480

2017

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Recurrent intestinal perforation associated with thrombosis of inferior vena cava: uncommon presentation of antiphospholipid syndrome

Journal of rheumatology, 2008-11, Vol.35 (11), p.2291

2008

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Germline mutations in the von Hippel–Lindau gene in Italian patients

European journal of medical genetics, 2009-09, Vol.52 (5), p.311-314

2009

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The spectrum of GNE mutations: allelic heterogeneity for a common phenotype

Neurological sciences, 2010-06, Vol.31 (3), p.377-380

2010

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Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case-control study

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-07, Vol.128B (1), p.27-29

2004

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A putative regulatory subunit (NR3A) of the NMDA receptor complex as candidate gene for susceptibility to schizophrenia: a case-control study

Psychiatric genetics, 2007-12, Vol.17 (6), p.355-356

2007

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Essential tremor is not associated with α-synuclein gene haplotypes

Movement disorders, 2003-07, Vol.18 (7), p.823-826

2003

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Essential tremor is not associated with a-synuclein gene haplotypes

Movement disorders, 2003-07, Vol.18 (7), p.823-826

2003

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Update upon efficacy and safety of etanercept for the treatment of spondyloarthritis and juvenile idiopathic arthritis

Current Views on Diagnostic Approach and Treatment of Lymphedema

HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients

Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise"

Severe Neuropathy After Diphtheria-Tetanus-Pertussis Vaccination in a Child Carrying a Novel Frame-Shift Mutation in the Small Heat-Shock Protein 27 Gene

Endothelial dysfunction in rheumatic autoimmune diseases

Gap junction beta 1 ( ) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease

TNF-α Gene Polymorphisms: Association with Disease Susceptibility and Response to Anti-TNF-α Treatment in Psoriatic Arthritis

Genetic factors and systemic sclerosis

Nocturia: An Uncommon Presentation of Lower-Limb Lymphedema

Update upon efficacy and safety of TNF-α inhibitors

TNF-[alpha] Gene Polymorphisms: Association with Disease Susceptibility and Response to Anti-TNF-[alpha] Treatment in Psoriatic Arthritis

A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot–Marie–Tooth disease

Pharmacogenetics and Future Therapeutic Scenarios: What Affects the Prediction of Response to Treatment with Etanercept?

Two novel cases of compound heterozygous mutations in mitofusin2: finding out the inheritance

Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: Findings in an Italian cohort of patients with Parkinsonian syndromes and relevance for genetic counselling

Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies

1993–2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa

Recurrent intestinal perforation associated with thrombosis of inferior vena cava: uncommon presentation of antiphospholipid syndrome

Germline mutations in the von Hippel–Lindau gene in Italian patients

The spectrum of GNE mutations: allelic heterogeneity for a common phenotype

Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case-control study

A putative regulatory subunit (NR3A) of the NMDA receptor complex as candidate gene for susceptibility to schizophrenia: a case-control study

Essential tremor is not associated with α-synuclein gene haplotypes

Essential tremor is not associated with a-synuclein gene haplotypes

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