Alessandro Rossi

Naples, Italy

Last Updated: 09/26/2026

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Found 62 publications

Phase 3 Randomized Trial Results of DTX401 AAV Gene Therapy for the Treatment of GSDIa.

Phase 3 Randomized Trial Results of DTX401 AAV Gene Therapy for the Treatment of GSDIa.

Journal: Journal of inherited metabolic disease
Published: April 29, 2026

Toward standardized care: International expert survey on pregnancy management in long-chain fatty acid oxidation disorders and unmet needs.

Toward standardized care: International expert survey on pregnancy management in long-chain fatty acid oxidation disorders and unmet needs.

Journal: Molecular genetics and metabolism
Published: April 29, 2026

Knowledge, attitudes, and practices in pediatric hypoglycemia in Italy (KAPPHy study).

Knowledge, attitudes, and practices in pediatric hypoglycemia in Italy (KAPPHy study).

Journal: Journal of endocrinological investigation
Published: March 26, 2026

Clinical and biochemical footprints of inherited metabolic disorders: XIX. Hypoglycemia.

Clinical and biochemical footprints of inherited metabolic disorders: XIX. Hypoglycemia.

Journal: Molecular genetics and metabolism
Published: January 26, 2026

Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American Survey.

Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American Survey.

Journal: Journal of inherited metabolic disease
Published: October 24, 2025

Variants in GSTZ1 Gene Underlying Maleylacetoacetate Isomerase Deficiency: Characterization of Two New Individuals and Literature Review.

Variants in GSTZ1 Gene Underlying Maleylacetoacetate Isomerase Deficiency: Characterization of Two New Individuals and Literature Review.

Journal: Genes
Published: July 21, 2025

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

Journal: Brain : a journal of neurology
Published: July 01, 2025

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

Journal: Brain : a journal of neurology
Published: July 01, 2025

Benefits and pitfalls in newborn screening for carnitine uptake deficiency: a 4-year single-center experience.

Benefits and pitfalls in newborn screening for carnitine uptake deficiency: a 4-year single-center experience.

Journal: Orphanet journal of rare diseases
Published: April 20, 2025

Multiomics approach provides insight into altered choline metabolism and liver injury in patients with glycogen storage disease type Ia.

Multiomics approach provides insight into altered choline metabolism and liver injury in patients with glycogen storage disease type Ia.

Journal: Scientific reports
Published: March 26, 2025

State of the art management practices for liver glycogen storage disorders: Results from an international survey among metabolic centres.

State of the art management practices for liver glycogen storage disorders: Results from an international survey among metabolic centres.

Journal: Molecular genetics and metabolism
Published: February 08, 2025

State of the Art and Consensus Statements by Healthcare Providers, Patients, and Caregivers on Continuous Glucose Monitoring in Liver Glycogen Storage Diseases.

State of the Art and Consensus Statements by Healthcare Providers, Patients, and Caregivers on Continuous Glucose Monitoring in Liver Glycogen Storage Diseases.

Journal: Journal of inherited metabolic disease
Published: February 04, 2025
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Last Updated: 09/26/2026