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Carlo Fusco

Showing results (41-50 of 148) with videos related to

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Brain & Development|July 22, 2017
KCNQ2 encephalopathy: A case due to a de novo deletionCarlotta Spagnoli, Grazia Gabriella Salerno, Alessandro Iodice, et al.
The Journal of Biological Chemistry|July 29, 2010
Transportin regulates nuclear import of CD44Michalina Janiszewska, Claudio De Vito, Marie-Aude Le Bitoux, et al.
Journal of Child Neurology|March 23, 2010
Transient basal ganglia and thalamic involvement following Mycoplasma pneumoniae infection associated with antiganglioside antibodiesCarlo Fusco, Elena Bonini, Giuliana Soncini, et al.
Plos One|December 22, 2006
A mouse stromal response to tumor invasion predicts prostate and breast cancer patient survivalMarina Bacac, Paolo Provero, Nathalie Mayran, et al.
Journal of Child Neurology|April 13, 2010
Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patientCarlo Fusco, Daniele Frattini, Francesco Pisani, et al.
Journal of Child Neurology|November 1, 2012
New Niemann-Pick type C1 gene mutation associated with very severe disease course and marked early cerebellar vermis atrophyCarlo Fusco, Angelo Russo, Daniela Galla, et al.
Molecular Syndromology|May 20, 2021
Pharmacological Treatment of Severe Breathing Abnormalities in a Case of <i>HNRNPU</i> Epileptic EncephalopathyCarlotta Spagnoli, Susanna Rizzi, Grazia Gabriella Salerno, et al.
International Journal of Molecular Sciences|May 27, 2026
PANDAS Syndrome: A Narrative Review of the Diagnostic Conundrum in Children with Acute Neuropsychiatric SymptomsCarlo Alberto Cesaroni, Giulia Pisanò, Susanna Rizzi, et al.
Mitochondrion|October 2, 2021
Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disordersGiuditta Pellino, Raffaella Faggioli, Anna Galuppi, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 5, 2021
SPG6 (NIPA1 variant): A report of a case with early-onset complex hereditary spastic paraplegia and brief literature reviewCarlotta Spagnoli, Silvia Schiavoni, Susanna Rizzi, et al.
Pageof 15

Showing results (41-50 of 148) with videos related to

Sort By:
Pageof 15
Brain & Development|July 22, 2017
KCNQ2 encephalopathy: A case due to a de novo deletionCarlotta Spagnoli, Grazia Gabriella Salerno, Alessandro Iodice, et al.
The Journal of Biological Chemistry|July 29, 2010
Transportin regulates nuclear import of CD44Michalina Janiszewska, Claudio De Vito, Marie-Aude Le Bitoux, et al.
Journal of Child Neurology|March 23, 2010
Transient basal ganglia and thalamic involvement following Mycoplasma pneumoniae infection associated with antiganglioside antibodiesCarlo Fusco, Elena Bonini, Giuliana Soncini, et al.
Plos One|December 22, 2006
A mouse stromal response to tumor invasion predicts prostate and breast cancer patient survivalMarina Bacac, Paolo Provero, Nathalie Mayran, et al.
Journal of Child Neurology|April 13, 2010
Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patientCarlo Fusco, Daniele Frattini, Francesco Pisani, et al.
Journal of Child Neurology|November 1, 2012
New Niemann-Pick type C1 gene mutation associated with very severe disease course and marked early cerebellar vermis atrophyCarlo Fusco, Angelo Russo, Daniela Galla, et al.
Molecular Syndromology|May 20, 2021
Pharmacological Treatment of Severe Breathing Abnormalities in a Case of <i>HNRNPU</i> Epileptic EncephalopathyCarlotta Spagnoli, Susanna Rizzi, Grazia Gabriella Salerno, et al.
International Journal of Molecular Sciences|May 27, 2026
PANDAS Syndrome: A Narrative Review of the Diagnostic Conundrum in Children with Acute Neuropsychiatric SymptomsCarlo Alberto Cesaroni, Giulia Pisanò, Susanna Rizzi, et al.
Mitochondrion|October 2, 2021
Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disordersGiuditta Pellino, Raffaella Faggioli, Anna Galuppi, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 5, 2021
SPG6 (NIPA1 variant): A report of a case with early-onset complex hereditary spastic paraplegia and brief literature reviewCarlotta Spagnoli, Silvia Schiavoni, Susanna Rizzi, et al.
Pageof 15