Alberto Lerario

Milan, 20122, Italy

Last Updated: 09/26/2026

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Found 16 publications

Combined omalizumab and desensitization to control IgE-mediated hypersensitivity in enzyme replacement therapy for late-onset Pompe disease.

Combined omalizumab and desensitization to control IgE-mediated hypersensitivity in enzyme replacement therapy for late-onset Pompe disease.

Journal: Orphanet journal of rare diseases
Published: October 23, 2025

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

Patient's punctuality in an outpatient clinic: the role of age, medical branch and geographical factors.

Patient's punctuality in an outpatient clinic: the role of age, medical branch and geographical factors.

Journal: BMC health services research
Published: June 09, 2023

Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD).

Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD).

Journal: Current issues in molecular biology
Published: March 02, 2023

Elevated Bone Resorption Markers in Patients With Migraine: A Case Series.

Elevated Bone Resorption Markers in Patients With Migraine: A Case Series.

Journal: Journal of clinical neurology (Seoul, Korea)
Published: July 01, 2022

Correction to: Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Correction to: Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: July 03, 2021

Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Unilateral freezing of gait or "magnetic feet phenomenon" caused by ischemic lesion involving fronto-striatal networks.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 23, 2021

Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophy.

Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophy.

Journal: European journal of neurology
Published: August 04, 2019

The Use of Social Media and Digital Devices Among Italian Neurologists.

The Use of Social Media and Digital Devices Among Italian Neurologists.

Journal: Frontiers in neurology
Published: July 06, 2019

MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form.

MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form.

Journal: Molecular genetics & genomic medicine
Published: May 16, 2019

Immune-mediated necrotizing myopathy due to statins exposure.

Immune-mediated necrotizing myopathy due to statins exposure.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Published: April 05, 2019

Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group.

Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group.

Journal: Advances in therapy
Published: January 19, 2019
Showing 1-12 of 16

Last Updated: 09/26/2026