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Medicina Clinica
|
February 9, 2010
[Utility of enzyme replacement therapy in Fabry disease]
Juan Manuel Politei, Alberto Dubrovsky
Muscle & Nerve
|
March 7, 2013
Pompe disease, the must-not-miss diagnosis: A report of 3 patients
Alberto Dubrovsky, Jose Corderi, Theodora Karasarides, et al.
Muscle & Nerve
|
September 29, 2011
Expanding the phenotype of late-onset Pompe disease: tongue weakness: a new clinical observation
Alberto Dubrovsky, Jose Corderi, Min Lin, et al.
Surgical Neurology International
|
August 29, 2014
[Thoracic Outlet Syndrome: is it always a surgical condition? Analysis of a series of 31 cases operated by the supraclavicular route]
Mariano Socolovsky, Gilda Di Masi, Daniela Binaghi, et al.
Frontiers in Pharmacology
|
June 21, 2021
Theragnosis for Duchenne Muscular Dystrophy
Leonela Luce, Micaela Carcione, Chiara Mazzanti, et al.
Muscle & Nerve
|
June 27, 2013
Generating color-coded anatomic muscle maps for correlation of quantitative magnetic resonance imaging analysis with clinical examination in neuromuscular disorders
Ramin Javan, Jeffrey J Horvath, Laura E Case, et al.
Archivos Argentinos De Pediatria
|
October 26, 2022
The difficult path to diagnosis of the patient with spinal muscular atrophy
Carla F Bolaño Díaz, Mariel Morosini, Fernando Chloca, et al.
American Journal of Physical Medicine & Rehabilitation
|
February 22, 2003
Nutritional assessment of patients with neuromuscular diseases
Fernando Augusto Pessolano, Adrián Alejandro Súarez, Sergio Gabriel Monteiro, et al.
American Journal of Physical Medicine & Rehabilitation
|
July 20, 2002
Peak flow and peak cough flow in the evaluation of expiratory muscle weakness and bulbar impairment in patients with neuromuscular disease
Adrián Alejandro Suárez, Fernando Augusto Pessolano, Sergio Gabriel Monteiro, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 14, 2024
Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: Findings from an Argentine patient cohort
Leonela Luce, Chiara Mazzanti, Micaela Carcione, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Medicina Clinica
|
February 9, 2010
[Utility of enzyme replacement therapy in Fabry disease]
Juan Manuel Politei, Alberto Dubrovsky
Muscle & Nerve
|
March 7, 2013
Pompe disease, the must-not-miss diagnosis: A report of 3 patients
Alberto Dubrovsky, Jose Corderi, Theodora Karasarides, et al.
Muscle & Nerve
|
September 29, 2011
Expanding the phenotype of late-onset Pompe disease: tongue weakness: a new clinical observation
Alberto Dubrovsky, Jose Corderi, Min Lin, et al.
Surgical Neurology International
|
August 29, 2014
[Thoracic Outlet Syndrome: is it always a surgical condition? Analysis of a series of 31 cases operated by the supraclavicular route]
Mariano Socolovsky, Gilda Di Masi, Daniela Binaghi, et al.
Frontiers in Pharmacology
|
June 21, 2021
Theragnosis for Duchenne Muscular Dystrophy
Leonela Luce, Micaela Carcione, Chiara Mazzanti, et al.
Muscle & Nerve
|
June 27, 2013
Generating color-coded anatomic muscle maps for correlation of quantitative magnetic resonance imaging analysis with clinical examination in neuromuscular disorders
Ramin Javan, Jeffrey J Horvath, Laura E Case, et al.
Archivos Argentinos De Pediatria
|
October 26, 2022
The difficult path to diagnosis of the patient with spinal muscular atrophy
Carla F Bolaño Díaz, Mariel Morosini, Fernando Chloca, et al.
American Journal of Physical Medicine & Rehabilitation
|
February 22, 2003
Nutritional assessment of patients with neuromuscular diseases
Fernando Augusto Pessolano, Adrián Alejandro Súarez, Sergio Gabriel Monteiro, et al.
American Journal of Physical Medicine & Rehabilitation
|
July 20, 2002
Peak flow and peak cough flow in the evaluation of expiratory muscle weakness and bulbar impairment in patients with neuromuscular disease
Adrián Alejandro Suárez, Fernando Augusto Pessolano, Sergio Gabriel Monteiro, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 14, 2024
Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: Findings from an Argentine patient cohort
Leonela Luce, Chiara Mazzanti, Micaela Carcione, et al.
Page
of 2