Ludovico Lispi

Rome, 00152, Italy

Last Updated: 09/26/2026

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Found 14 publications

NEFL-Related Charcot-Marie Tooth Disease due to P440L Mutation in Two Italian Families: Expanding the Phenotype and Defining Modulating Factors.

NEFL-Related Charcot-Marie Tooth Disease due to P440L Mutation in Two Italian Families: Expanding the Phenotype and Defining Modulating Factors.

Journal: European neurology

Published: October 13, 2022

Moving breast implant registries forward: Are they FAIR and Functional?

Moving breast implant registries forward: Are they FAIR and Functional?

Journal: Journal of plastic, reconstructive & aesthetic surgery : JPRAS

Published: November 22, 2019

Electrophysiological abnormalities in iatrogenic botulism: Two case reports and review of the literature.

Electrophysiological abnormalities in iatrogenic botulism: Two case reports and review of the literature.

Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia

Published: August 21, 2018

Clinical and genetic characterization of an Italian family with slow-channel syndrome.

Clinical and genetic characterization of an Italian family with slow-channel syndrome.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: May 15, 2018

Impact of Mézières Rehabilitative Method in Patients with Parkinson's Disease: A Randomized Controlled Trial.

Impact of Mézières Rehabilitative Method in Patients with Parkinson's Disease: A Randomized Controlled Trial.

Journal: Parkinson's disease

Published: June 30, 2017

Longitudinal neurophysiological assessment of intramuscular type-A botulin toxin in healthy humans.

Longitudinal neurophysiological assessment of intramuscular type-A botulin toxin in healthy humans.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: June 28, 2017

ATP1A3 mutant patient with alternating hemiplegia of childhood and brain spectroscopic abnormalities.

ATP1A3 mutant patient with alternating hemiplegia of childhood and brain spectroscopic abnormalities.

Journal: Journal of the neurological sciences

Published: March 06, 2017

Mobility trends of Patients across Italian Regions: implications for planning and evaluation of hospital services.

Mobility trends of Patients across Italian Regions: implications for planning and evaluation of hospital services.

Journal: Annali di igiene : medicina preventiva e di comunita

Published: September 15, 2016

Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling.

Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling.

Journal: Human molecular genetics

Published: May 27, 2016

Neuromuscular transmission abnormalities in myotonic dystrophy type 1: A neurophysiological study.

Neuromuscular transmission abnormalities in myotonic dystrophy type 1: A neurophysiological study.

Journal: Clinical neurology and neurosurgery

Published: May 21, 2016

Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features--a case report.

Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features--a case report.

Journal: BMC medical genetics

Published: November 17, 2015

How genetics affects the brain to produce higher-level dysfunctions in myotonic dystrophy type 1.

How genetics affects the brain to produce higher-level dysfunctions in myotonic dystrophy type 1.

Journal: Functional neurology

Published: July 28, 2015

Showing 1-12 of 14

Last Updated: 09/26/2026