Andrea Barp

London, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 48 publications

Assessment of IBM-FRS total score and specific functional domains in a large cohort of inclusion body myositis patients.

Assessment of IBM-FRS total score and specific functional domains in a large cohort of inclusion body myositis patients.

Journal: Journal of neurology
Published: September 08, 2025

Impact of nursing robotic assisted surgery education on Kirkpatrick's four levels.

Impact of nursing robotic assisted surgery education on Kirkpatrick's four levels.

Journal: Frontiers in surgery
Published: May 30, 2025

Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular Dystrophy.

Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular Dystrophy.

Journal: Drugs in R&D
Published: May 04, 2025

A novel deep intronic mutation expands the genotype spectrum of MYH7-related myopathies.

A novel deep intronic mutation expands the genotype spectrum of MYH7-related myopathies.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: April 29, 2025

Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfa.

Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfa.

Journal: Journal of neurology
Published: March 03, 2025

Exclusion of CLIC5 as a Candidate Gene and Identification of NEFM as a Possible Novel Gene Correlated With Autosomal Recessive Pure Cerebellar Ataxia in a Highly Consanguineous Family.

Exclusion of CLIC5 as a Candidate Gene and Identification of NEFM as a Possible Novel Gene Correlated With Autosomal Recessive Pure Cerebellar Ataxia in a Highly Consanguineous Family.

Journal: Molecular genetics & genomic medicine
Published: February 11, 2025

Neurogenic disease with high CK: think muscle.

Neurogenic disease with high CK: think muscle.

Journal: Practical neurology
Published: November 16, 2024

Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey.

Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey.

Journal: European journal of pediatrics
Published: August 01, 2024

Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity.

Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity.

Journal: Brain : a journal of neurology
Published: July 08, 2024

The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy.

The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy.

Journal: Journal of neuromuscular diseases
Published: February 16, 2024

Parkinsonism may aggravate dysphagia in myotonic dystrophy type 1: two case reports.

Parkinsonism may aggravate dysphagia in myotonic dystrophy type 1: two case reports.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: February 22, 2023

Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle.

Facial nerve vulnerability in spinal muscular atrophy and motor unit number index of the orbicularis oculi muscle.

Journal: Muscle & nerve
Published: December 01, 2022
Showing 1-12 of 48

Last Updated: 09/26/2026