Rossella Gulli

Genoa, 16132, Italy

Last Updated: 09/26/2026

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Found 14 publications

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

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

Journal: Orphanet journal of rare diseases

Published: July 20, 2018

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

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

Journal: Modern rheumatology

Published: August 25, 2017

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

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

Journal: Neuromuscular disorders : NMD

Published: August 01, 2016

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

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

Journal: Molecular genetics & genomic medicine

Published: April 13, 2016

Genetic factors and systemic sclerosis.

Genetic factors and systemic sclerosis.

Journal: Autoimmunity reviews

Published: January 06, 2016

GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course.

GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course.

Journal: Neuromuscular disorders : NMD

Published: April 28, 2015

Pharmacogenetics and future therapeutic scenarios: what affects the prediction of response to treatment with etanercept?

Pharmacogenetics and future therapeutic scenarios: what affects the prediction of response to treatment with etanercept?

Journal: Drug development research

Published: November 11, 2014

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

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

Journal: Journal of the neurological sciences

Published: February 04, 2014

Contribution of copy number variations in CMT1X: a retrospective study.

Contribution of copy number variations in CMT1X: a retrospective study.

Journal: European journal of neurology

Published: January 08, 2014

TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis.

TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis.

Journal: The Journal of investigative dermatology

Published: September 26, 2013

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.

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.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: March 21, 2013

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

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

Journal: Journal of the peripheral nervous system : JPNS

Published: December 20, 2011

Showing 1-12 of 14

Last Updated: 09/26/2026