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S Monges

Showing results (1-10 of 9) with videos related to

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Gene Therapy|July 29, 2017
Management of neuromuscular diseases and spinal muscular atrophy in Latin AmericaS Monges, A L Rosa
Revista De Neurologia|October 9, 2003
[Delayed-type subacute measles encephalitis]R Caraballo, S Monges, R Cersósimo, et al.
Revista De Neurologia|March 18, 2003
[Reflex myoclonic epilepsy in infancy: a new reflex epilepsy syndrome or a variant of benign myoclonic epilepsy in infancy]R Caraballo, L Cassar, S Monges, et al.
Journal of Neuromuscular Diseases|September 14, 2020
Natural History of Type 1 Spinal Muscular Atrophy in a Series of Argentinian ChildrenV Aguerre, F De Castro, J Mozzoni, et al.
Leukemia Research|January 13, 2018
Acute and sub-acute neurological toxicity in children treated for acute lymphoblastic leukemiaNatalia C Millan, Analía Pastrana, Myriam R Guitter, et al.
Revista De Neurologia|March 8, 2005
[Clinical and electroencephalographic aspects of late infantile neuronal ceroid lipofuscinosis]R Caraballo, A Sologuestua, V L Ruggieri, et al.
Neuromuscular Disorders : NMD|October 17, 2017
Corrigendum to "22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd-7th October 2017" [Neuromuscular Disorders 27S2 (2017) S51-S270]J Rendu, C Bosson, N Roux-Buisson, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locusN B Romero, M Herasse, N Monnier, et al.
Neuropathology and Applied Neurobiology|November 11, 2010
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganizationJ A Bevilacqua, N Monnier, M Bitoun, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Gene Therapy|July 29, 2017
Management of neuromuscular diseases and spinal muscular atrophy in Latin AmericaS Monges, A L Rosa
Revista De Neurologia|October 9, 2003
[Delayed-type subacute measles encephalitis]R Caraballo, S Monges, R Cersósimo, et al.
Revista De Neurologia|March 18, 2003
[Reflex myoclonic epilepsy in infancy: a new reflex epilepsy syndrome or a variant of benign myoclonic epilepsy in infancy]R Caraballo, L Cassar, S Monges, et al.
Journal of Neuromuscular Diseases|September 14, 2020
Natural History of Type 1 Spinal Muscular Atrophy in a Series of Argentinian ChildrenV Aguerre, F De Castro, J Mozzoni, et al.
Leukemia Research|January 13, 2018
Acute and sub-acute neurological toxicity in children treated for acute lymphoblastic leukemiaNatalia C Millan, Analía Pastrana, Myriam R Guitter, et al.
Revista De Neurologia|March 8, 2005
[Clinical and electroencephalographic aspects of late infantile neuronal ceroid lipofuscinosis]R Caraballo, A Sologuestua, V L Ruggieri, et al.
Neuromuscular Disorders : NMD|October 17, 2017
Corrigendum to "22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd-7th October 2017" [Neuromuscular Disorders 27S2 (2017) S51-S270]J Rendu, C Bosson, N Roux-Buisson, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locusN B Romero, M Herasse, N Monnier, et al.
Neuropathology and Applied Neurobiology|November 11, 2010
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganizationJ A Bevilacqua, N Monnier, M Bitoun, et al.
Pageof 1