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Lucilla Nobbio

Showing results (31-40 of 39) with videos related to

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Frontiers in Neurology|September 28, 2020
Exploiting Sphingo- and Glycerophospholipid Impairment to Select Effective Drugs and Biomarkers for CMT1ADavide Visigalli, Giovanna Capodivento, Abdul Basit, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2020
CSF sphingomyelin: a new biomarker of demyelination in the diagnosis and management of CIDP and GBSGiovanna Capodivento, Chiara De Michelis, Marinella Carpo, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 15, 2025
Exposure of dams to Elexacaftor/ Tezacaftor/Ivacaftor during pregnancy and breastfeeding induces reversible alterations in newborn wild type CD-1 miceAngelica Squarzoni, Gaia Boschetti, Sine Mandrup Bertozzi, et al.
Biomarker Insights|July 8, 2025
A Comprehensive Description of the Roadmap to Identify and Validate a Myelin BiomarkerGiovanna Capodivento, Davide Visigalli, Andrea Armirotti, et al.
Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, et al.
Molecular and Cellular Neurosciences|September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neuronsNathalie Verpoorten, Kristien Verhoeven, Stefan Weckx, et al.
Life (Basel, Switzerland)|March 25, 2022
Genetic Workup for Charcot-Marie-Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 YearsChiara Gemelli, Alessandro Geroldi, Sara Massucco, et al.
Biomolecules|June 26, 2025
Increased [<sup>18</sup>F]DPA-714 Uptake in the Skeletal Muscle of SOD1<sup>G93A</sup> Mice: A New Potential of Translocator Protein 18 kDa Imaging in Amyotrophic Lateral SclerosisCecilia Marini, Mattia Riondato, Edoardo Dighero, et al.
Neuropathology and Applied Neurobiology|July 29, 2022
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatmentChiara Fiorillo, Giovanna Capodivento, Alessandro Geroldi, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Frontiers in Neurology|September 28, 2020
Exploiting Sphingo- and Glycerophospholipid Impairment to Select Effective Drugs and Biomarkers for CMT1ADavide Visigalli, Giovanna Capodivento, Abdul Basit, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2020
CSF sphingomyelin: a new biomarker of demyelination in the diagnosis and management of CIDP and GBSGiovanna Capodivento, Chiara De Michelis, Marinella Carpo, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 15, 2025
Exposure of dams to Elexacaftor/ Tezacaftor/Ivacaftor during pregnancy and breastfeeding induces reversible alterations in newborn wild type CD-1 miceAngelica Squarzoni, Gaia Boschetti, Sine Mandrup Bertozzi, et al.
Biomarker Insights|July 8, 2025
A Comprehensive Description of the Roadmap to Identify and Validate a Myelin BiomarkerGiovanna Capodivento, Davide Visigalli, Andrea Armirotti, et al.
Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, et al.
Molecular and Cellular Neurosciences|September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neuronsNathalie Verpoorten, Kristien Verhoeven, Stefan Weckx, et al.
Life (Basel, Switzerland)|March 25, 2022
Genetic Workup for Charcot-Marie-Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 YearsChiara Gemelli, Alessandro Geroldi, Sara Massucco, et al.
Biomolecules|June 26, 2025
Increased [<sup>18</sup>F]DPA-714 Uptake in the Skeletal Muscle of SOD1<sup>G93A</sup> Mice: A New Potential of Translocator Protein 18 kDa Imaging in Amyotrophic Lateral SclerosisCecilia Marini, Mattia Riondato, Edoardo Dighero, et al.
Neuropathology and Applied Neurobiology|July 29, 2022
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatmentChiara Fiorillo, Giovanna Capodivento, Alessandro Geroldi, et al.
Pageof 4