Domenico Garozzo

Catania, 95126, Italy

Last Updated: 09/26/2026

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Found 67 publications

IgG Glycosylation Analysis in Patients with Ring14 Syndrome Unveils Novel Pathomechanisms and New Therapy Perspectives.

IgG Glycosylation Analysis in Patients with Ring14 Syndrome Unveils Novel Pathomechanisms and New Therapy Perspectives.

Journal: Biomolecules

Published: April 01, 2026

Mono-allelic p.R37H Dehydrodolichyl Diphosphate Synthase variants lead to protein glycosylation defects, aberrant lipid profiles and interneuron scarcity in a novel mouse model of progressive epileptic encephalopathy.

Mono-allelic p.R37H Dehydrodolichyl Diphosphate Synthase variants lead to protein glycosylation defects, aberrant lipid profiles and interneuron scarcity in a novel mouse model of progressive epileptic encephalopathy.

Journal: bioRxiv : the preprint server for biology

Published: September 02, 2025

Unveiling the structure of Delftia acidovorans Lipopolysaccharide: insights into O-antigen and lipid A.

Unveiling the structure of Delftia acidovorans Lipopolysaccharide: insights into O-antigen and lipid A.

Journal: Carbohydrate research

Published: April 11, 2025

In Reply: Thoracic Outlet Syndrome Part I: Systematic Review of the Literature and Consensus on Anatomy, Diagnosis, and Classification of Thoracic Outlet Syndrome, and Thoracic Outlet Syndrome Part II: Consensus on the Management of Thoracic Outlet Syndrome by the European Association of Neurosurgical Societies' Section of Peripheral Nerve Surgery.

In Reply: Thoracic Outlet Syndrome Part I: Systematic Review of the Literature and Consensus on Anatomy, Diagnosis, and Classification of Thoracic Outlet Syndrome, and Thoracic Outlet Syndrome Part II: Consensus on the Management of Thoracic Outlet Syndrome by the European Association of Neurosurgical Societies' Section of Peripheral Nerve Surgery.

Journal: Neurosurgery

Published: May 13, 2024

Secondary deficiency of neuraminidase 1 contributes to CNS pathology in neurological mucopolysaccharidoses via hypersialylation of brain glycoproteins.

Secondary deficiency of neuraminidase 1 contributes to CNS pathology in neurological mucopolysaccharidoses via hypersialylation of brain glycoproteins.

Journal: bioRxiv : the preprint server for biology

Published: May 07, 2024

CSF N-Glycomics Using MALDI MS Techniques.

CSF N-Glycomics Using MALDI MS Techniques.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: March 01, 2024

CSF N-Glycomics Using High-Throughput UPLC-ESI Techniques in Alzheimer's Disease.

CSF N-Glycomics Using High-Throughput UPLC-ESI Techniques in Alzheimer's Disease.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: March 01, 2024

Neuraminidase 1 secondary deficiency contributes to CNS pathology in neurological mucopolysaccharidoses via brain protein hypersialylation.

Neuraminidase 1 secondary deficiency contributes to CNS pathology in neurological mucopolysaccharidoses via brain protein hypersialylation.

Journal: The Journal of clinical investigation

Published: January 26, 2024

Integrative multidisciplinary approaches by the Integrative Medicine Research Group (IMRG): a new frontier in cancer setting.

Integrative multidisciplinary approaches by the Integrative Medicine Research Group (IMRG): a new frontier in cancer setting.

Journal: European review for medical and pharmacological sciences

Published: November 17, 2023

N-acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and function.

N-acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and function.

Journal: Science advances

Published: June 30, 2023

Soluble peptidoglycan fragments produced by Limosilactobacillus fermentum with antiproliferative activity are suitable for potential therapeutic development: A preliminary report.

Soluble peptidoglycan fragments produced by Limosilactobacillus fermentum with antiproliferative activity are suitable for potential therapeutic development: A preliminary report.

Journal: Frontiers in molecular biosciences

Published: October 28, 2022

Severe kidney dysfunction in sialidosis mice reveals an essential role for neuraminidase 1 in reabsorption.

Severe kidney dysfunction in sialidosis mice reveals an essential role for neuraminidase 1 in reabsorption.

Journal: JCI insight

Published: October 24, 2022

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Last Updated: 09/26/2026