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Mario Sabatelli

Showing results (71-80 of 179) with videos related to

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ESC Heart Failure|June 12, 2019
Sustained safe and effective anticoagulation using Edoxaban via percutaneous endoscopic gastrostomyMattia Galli, Domenico D'Amario, Felicita Andreotti, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|December 8, 2010
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathyMarco Luigetti, Amelia Conte, Francesca Madia, et al.
Muscle & Nerve|January 8, 2014
Ultrasound evaluation in transthyretin-related amyloid neuropathyGiuseppe Granata, Marco Luigetti, Daniele Coraci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 18, 2012
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patientsMarco Luigetti, Amelia Conte, Alessandra Del Grande, et al.
American Journal of Hematology|April 11, 2012
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantationBarbara Vannata, Luca Laurenti, Patrizia Chiusolo, et al.
Cells|October 19, 2019
The S100A4 Transcriptional Inhibitor Niclosamide Reduces Pro-Inflammatory and Migratory Phenotypes of Microglia: Implications for Amyotrophic Lateral SclerosisAlessia Serrano, Savina Apolloni, Simona Rossi, et al.
Muscle & Nerve|July 22, 2008
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsiesMarco Luigetti, Amelia Conte, Francesca Madia, et al.
Stem Cell Research|June 6, 2022
Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementiaFrancesco Martello, Serena Lattante, Paolo Niccolò Doronzio, et al.
Neuromuscular Disorders : NMD|August 17, 2010
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutationGiorgio Tasca, Massimiliano Mirabella, Aldobrando Broccolini, et al.
Brain Stimulation|July 17, 2010
Long-term motor cortex stimulation for amyotrophic lateral sclerosisVincenzo Di Lazzaro, Michele Dileone, Fabio Pilato, et al.
Pageof 18

Showing results (71-80 of 179) with videos related to

Sort By:
Pageof 18
ESC Heart Failure|June 12, 2019
Sustained safe and effective anticoagulation using Edoxaban via percutaneous endoscopic gastrostomyMattia Galli, Domenico D'Amario, Felicita Andreotti, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|December 8, 2010
Abnormal vascular smooth muscle cell proliferation in sural nerve biopsy from a patient with sensorimotor axonal neuropathyMarco Luigetti, Amelia Conte, Francesca Madia, et al.
Muscle & Nerve|January 8, 2014
Ultrasound evaluation in transthyretin-related amyloid neuropathyGiuseppe Granata, Marco Luigetti, Daniele Coraci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 18, 2012
TTR-related amyloid neuropathy: clinical, electrophysiological and pathological findings in 15 unrelated patientsMarco Luigetti, Amelia Conte, Alessandra Del Grande, et al.
American Journal of Hematology|April 11, 2012
Efficacy of lenalidomide plus dexamethasone for POEMS syndrome relapsed after autologous peripheral stem-cell transplantationBarbara Vannata, Luca Laurenti, Patrizia Chiusolo, et al.
Cells|October 19, 2019
The S100A4 Transcriptional Inhibitor Niclosamide Reduces Pro-Inflammatory and Migratory Phenotypes of Microglia: Implications for Amyotrophic Lateral SclerosisAlessia Serrano, Savina Apolloni, Simona Rossi, et al.
Muscle & Nerve|July 22, 2008
A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsiesMarco Luigetti, Amelia Conte, Francesca Madia, et al.
Stem Cell Research|June 6, 2022
Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementiaFrancesco Martello, Serena Lattante, Paolo Niccolò Doronzio, et al.
Neuromuscular Disorders : NMD|August 17, 2010
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutationGiorgio Tasca, Massimiliano Mirabella, Aldobrando Broccolini, et al.
Brain Stimulation|July 17, 2010
Long-term motor cortex stimulation for amyotrophic lateral sclerosisVincenzo Di Lazzaro, Michele Dileone, Fabio Pilato, et al.
Pageof 18