Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Marcelo Miranda

Showing results (71-80 of 111) with videos related to

Pageof 12
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2006
CADASIL presenting with a movement disorder: a clinical study of a Chilean kindredMarcelo Miranda, Martin Dichgans, Andrea Slachevsky, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2007
Phenotypic variability of a distinct deletion in McLeod syndromeMarcelo Miranda, Claudia Castiglioni, Beat M Frey, et al.
Revista Medica De Chile|October 15, 2013
[The use of e-mail in the communication between physicians and their patients]Marcelo Miranda C, Enrique Jadresic M, May Chomali G, et al.
Revista Medica De Chile|August 29, 2003
[Treatment of restless legs syndrome in uremic patients undergoing dialysis with pramipexole: preliminary results]Marcelo Miranda, Larisa Fabres, Marianne Kägi, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|December 18, 2013
Association of insulin resistance and GLP-2 secretion in obesity: a pilot studyBruno Geloneze, Marcelo Miranda de Oliveira Lima, José Carlos Pareja, et al.
Revista Medica De Chile|April 30, 2024
[Late-Onset Cerebellar Ataxia with Neuropathy: Uncovering the Role of RFC1 Gene Mutations]Marcelo Miranda C, Mario Diaz, Ricardo Hughes G, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 27, 2015
Pyruvate dehydrogenase deficiency presenting as isolated paroxysmal exercise induced dystonia successfully reversed with thiamine supplementation. Case report and mini-reviewClaudia Castiglioni, Daniela Verrigni, Cecilia Okuma, et al.
Cerebellum (London, England)|March 2, 2021
Autosomal Recessive Cerebellar Ataxia 1: First Case Report Depicting a Variant in SYNE1 Gene in a Chilean PatientJ Valentina Castillo, S Catherine Díaz, María Leonor Bustamante, et al.
Parkinsonism & Related Disorders|October 13, 2020
Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegiaMarcelo Miranda, Florian Harmuth, M Leonor Bustamante, et al.
Arquivos Brasileiros De Cardiologia|September 23, 2003
Safety, feasibility, and results of exercise testing for stratifying patients with chest pain in the emergency roomRenato Machado Macaciel, Evandro Tinoco Mesquita, Ricardo Vivacqua, et al.
Pageof 12

Showing results (71-80 of 111) with videos related to

Sort By:
Pageof 12
Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2006
CADASIL presenting with a movement disorder: a clinical study of a Chilean kindredMarcelo Miranda, Martin Dichgans, Andrea Slachevsky, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 2007
Phenotypic variability of a distinct deletion in McLeod syndromeMarcelo Miranda, Claudia Castiglioni, Beat M Frey, et al.
Revista Medica De Chile|October 15, 2013
[The use of e-mail in the communication between physicians and their patients]Marcelo Miranda C, Enrique Jadresic M, May Chomali G, et al.
Revista Medica De Chile|August 29, 2003
[Treatment of restless legs syndrome in uremic patients undergoing dialysis with pramipexole: preliminary results]Marcelo Miranda, Larisa Fabres, Marianne Kägi, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|December 18, 2013
Association of insulin resistance and GLP-2 secretion in obesity: a pilot studyBruno Geloneze, Marcelo Miranda de Oliveira Lima, José Carlos Pareja, et al.
Revista Medica De Chile|April 30, 2024
[Late-Onset Cerebellar Ataxia with Neuropathy: Uncovering the Role of RFC1 Gene Mutations]Marcelo Miranda C, Mario Diaz, Ricardo Hughes G, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 27, 2015
Pyruvate dehydrogenase deficiency presenting as isolated paroxysmal exercise induced dystonia successfully reversed with thiamine supplementation. Case report and mini-reviewClaudia Castiglioni, Daniela Verrigni, Cecilia Okuma, et al.
Cerebellum (London, England)|March 2, 2021
Autosomal Recessive Cerebellar Ataxia 1: First Case Report Depicting a Variant in SYNE1 Gene in a Chilean PatientJ Valentina Castillo, S Catherine Díaz, María Leonor Bustamante, et al.
Parkinsonism & Related Disorders|October 13, 2020
Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegiaMarcelo Miranda, Florian Harmuth, M Leonor Bustamante, et al.
Arquivos Brasileiros De Cardiologia|September 23, 2003
Safety, feasibility, and results of exercise testing for stratifying patients with chest pain in the emergency roomRenato Machado Macaciel, Evandro Tinoco Mesquita, Ricardo Vivacqua, et al.
Pageof 12