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Cells|September 26, 2025
Wings of Discovery: Using <i>Drosophila</i> to Decode Hereditary Spastic Paraplegia and AtaxiasRachele Vivarelli, Chiara Vantaggiato, Maria Teresa Bassi, et al.
International Journal of Molecular Sciences|March 13, 2024
Pluripotent Stem Cells as a Preclinical Cellular Model for Studying Hereditary Spastic ParaplegiasDevid Damiani, Matteo Baggiani, Stefania Della Vecchia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 17, 2023
Early-onset motor polyneuropathy associated with a novel dominant NAGLU mutationDiego Lopergolo, Simona Salvatore, Vincenzo Sorrentino, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 20, 2023
Enhanced expression of the autophagosomal marker LC3-II in detergent-resistant protein lysates from a CLN3 patient's post-mortem brainFrancesco Pezzini, Michele Fiorini, Stefano Doccini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 10, 2019
SPG8 mutations in Italian families: clinical data and literature reviewFederica Ginanneschi, Angelica D'Amore, Melissa Barghigiani, et al.
Genes|January 28, 2026
Interstitial 12p Deletion Syndrome: Revised Minimal Critical Region and Review of the LiteratureFlavia Privitera, Stefano Pagano, Lorenzo Cipriano, et al.
Biology|April 26, 2024
Zebrafish Feed Intake: A Systematic Review for Standardizing Feeding Management in Laboratory ConditionsRosario Licitra, Baldassare Fronte, Tiziano Verri, et al.
Stem Cell Research|June 18, 2024
Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 geneMatteo Baggiani, Filippo Maria Santorelli, Serena Mero, et al.
International Journal of Molecular Sciences|October 16, 2024
Generation and Characterization of hiPS Lines from Three Patients Affected by Different Forms of <i>HPDL</i>-Related Neurological DisordersMatteo Baggiani, Devid Damiani, Flavia Privitera, et al.
Orphanet Journal of Rare Diseases|June 16, 2026
Psychiatric manifestations in Neuronal ceroid lipofuscinosesStefania Della Vecchia, Alessandro Simonati, Maria Marchese, et al.
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