Generoso Andria

Naples, Italy

Last Updated: 09/26/2026

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Found 48 publications

Liver-Directed Adeno-Associated Virus-Mediated Gene Therapy for Mucopolysaccharidosis Type VI.

Liver-Directed Adeno-Associated Virus-Mediated Gene Therapy for Mucopolysaccharidosis Type VI.

Journal: NEJM evidence

Published: July 01, 2022

Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry.

Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry.

Journal: Journal of public health (Oxford, England)

Published: April 06, 2021

Parkinson's disease in Gaucher disease patients: what's changing in the counseling and management of patients and their relatives?

Parkinson's disease in Gaucher disease patients: what's changing in the counseling and management of patients and their relatives?

Journal: Orphanet journal of rare diseases

Published: May 12, 2020

Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report.

Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report.

Journal: Neuromuscular disorders : NMD

Published: June 01, 2018

Cardiologists and mucopolysaccharidoses. Recommendations of GICEM (Cardiology Experts on Metabolic Disease Italian Group) for diagnosis, follow-up and cardiological management

Cardiologists and mucopolysaccharidoses. Recommendations of GICEM (Cardiology Experts on Metabolic Disease Italian Group) for diagnosis, follow-up and cardiological management

Journal: Giornale italiano di cardiologia (2006)

Published: August 29, 2017

Cutting Edge: Increased Autoimmunity Risk in Glycogen Storage Disease Type 1b Is Associated with a Reduced Engagement of Glycolysis in T Cells and an Impaired Regulatory T Cell Function.

Cutting Edge: Increased Autoimmunity Risk in Glycogen Storage Disease Type 1b Is Associated with a Reduced Engagement of Glycolysis in T Cells and an Impaired Regulatory T Cell Function.

Journal: Journal of immunology (Baltimore, Md. : 1950)

Published: November 17, 2016

Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.

Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.

Journal: Journal of inherited metabolic disease

Published: May 23, 2016

The contribution of the citrate pathway to oxidative stress in Down syndrome.

The contribution of the citrate pathway to oxidative stress in Down syndrome.

Journal: Immunology

Published: February 07, 2016

New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.

New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.

Journal: Italian journal of pediatrics

Published: October 20, 2015

Reduced bone mineral density in glycogen storage disease type III: evidence for a possible connection between metabolic imbalance and bone homeostasis.

Reduced bone mineral density in glycogen storage disease type III: evidence for a possible connection between metabolic imbalance and bone homeostasis.

Journal: Bone

Published: August 07, 2015

Pharmacological Chaperone Therapy: Preclinical Development, Clinical Translation, and Prospects for the Treatment of Lysosomal Storage Disorders.

Pharmacological Chaperone Therapy: Preclinical Development, Clinical Translation, and Prospects for the Treatment of Lysosomal Storage Disorders.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: February 19, 2015

Targeted metabolomics in the expanded newborn screening for inborn errors of metabolism.

Targeted metabolomics in the expanded newborn screening for inborn errors of metabolism.

Journal: Molecular bioSystems

Published: February 18, 2015

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Last Updated: 09/26/2026