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Marina Frasquet

Showing results (1-10 of 21) with videos related to

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Current Opinion in Neurology|August 9, 2022
Hereditary motor neuropathiesMarina Frasquet, Teresa Sevilla
Brain : a Journal of Neurology|June 23, 2016
The role of DNAJB2 in amyotrophic lateral sclerosisMarina Frasquet, Juan F Vázquez-Costa, Teresa Sevilla
Journal of the Neurological Sciences|January 8, 2013
Embolism and impaired washout: a possible explanation of border zone strokes in hypereosinophilic syndromeLago Aida, Vera Parkhutik, Jose Ignacio Tembl, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 27, 2023
Eculizumab for a catastrophic relapse in NMOSD: case reportDavid Gorriz, Francisco Carlos Pérez-Miralles, Carlos Quintanilla-Bordás, et al.
Journal of the Neurological Sciences|March 25, 2018
Phenotypical features of two patients diagnosed with PHARC syndrome and carriers of a new homozygous mutation in the ABHD12 geneMarina Frasquet, Vincenzo Lupo, María José Chumillas, et al.
Neurology|October 17, 2020
Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor NeuropathyHerminia Argente-Escrig, Joshua Burns, Gabrielle Donlevy, et al.
Frontiers in Neurology|January 4, 2021
Early Referral to an ALS Center Reduces Several Months the Diagnostic Delay: A Multicenter-Based StudyMarina Martínez-Molina, Herminia Argente-Escrig, Margarita F Polo, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 21, 2019
Facial onset sensory and motor neuronopathy: a motor neuron disease with an oligogenic origin?Juan Francisco Vázquez-Costa, Laia Pedrola Vidal, Sarah Moreau-Le Lan, et al.
Annals of Clinical and Translational Neurology|July 29, 2021
Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral centerHerminia Argente-Escrig, Marina Frasquet, Juan Francisco Vázquez-Costa, et al.
Journal of the Neurological Sciences|June 2, 2019
A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4Herminia Argente-Escrig, Ana Sánchez-Monteagudo, Marina Frasquet, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Current Opinion in Neurology|August 9, 2022
Hereditary motor neuropathiesMarina Frasquet, Teresa Sevilla
Brain : a Journal of Neurology|June 23, 2016
The role of DNAJB2 in amyotrophic lateral sclerosisMarina Frasquet, Juan F Vázquez-Costa, Teresa Sevilla
Journal of the Neurological Sciences|January 8, 2013
Embolism and impaired washout: a possible explanation of border zone strokes in hypereosinophilic syndromeLago Aida, Vera Parkhutik, Jose Ignacio Tembl, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 27, 2023
Eculizumab for a catastrophic relapse in NMOSD: case reportDavid Gorriz, Francisco Carlos Pérez-Miralles, Carlos Quintanilla-Bordás, et al.
Journal of the Neurological Sciences|March 25, 2018
Phenotypical features of two patients diagnosed with PHARC syndrome and carriers of a new homozygous mutation in the ABHD12 geneMarina Frasquet, Vincenzo Lupo, María José Chumillas, et al.
Neurology|October 17, 2020
Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor NeuropathyHerminia Argente-Escrig, Joshua Burns, Gabrielle Donlevy, et al.
Frontiers in Neurology|January 4, 2021
Early Referral to an ALS Center Reduces Several Months the Diagnostic Delay: A Multicenter-Based StudyMarina Martínez-Molina, Herminia Argente-Escrig, Margarita F Polo, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 21, 2019
Facial onset sensory and motor neuronopathy: a motor neuron disease with an oligogenic origin?Juan Francisco Vázquez-Costa, Laia Pedrola Vidal, Sarah Moreau-Le Lan, et al.
Annals of Clinical and Translational Neurology|July 29, 2021
Pediatric inherited peripheral neuropathy: a prospective study at a Spanish referral centerHerminia Argente-Escrig, Marina Frasquet, Juan Francisco Vázquez-Costa, et al.
Journal of the Neurological Sciences|June 2, 2019
A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4Herminia Argente-Escrig, Ana Sánchez-Monteagudo, Marina Frasquet, et al.
Pageof 3