Search research articles
Contact Us
Filters
Showing results (1-10 of 14) with videos related to
Page
of 2
Sort By:
Revista Brasileira De Ortopedia
|
August 1, 2019
Limb Length Discrepancy on an 11-Month-Old Boy with Osteoid Osteoma
Ana Cotta, Renato Cesar Rezende de Castro, Julia Filardi Paim, et al.
Arquivos De Neuro-Psiquiatria
|
September 25, 2014
Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Ana Cotta, Elmano Carvalho, Antonio Lopes da-Cunha-Júnior, et al.
Journal of Molecular Neuroscience : MN
|
August 15, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability
Ana Cotta, Julia F Paim, Elmano Carvalho, et al.
Journal of Molecular Neuroscience : MN
|
March 13, 2013
Muscle phenotypic variability in limb girdle muscular dystrophy 2 G
Julia F Paim, Ana Cotta, Antonio P Vargas, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
January 18, 2021
Dominant or recessive mutations in the <i>RYR1</i> gene causing central core myopathy in Brazilian patients
Leonardo Galleni Leão, Lucas Santos Souza, Letícia Nogueira, et al.
Arquivos De Neuro-Psiquiatria
|
December 14, 2017
The relative frequency of common neuromuscular diagnoses in a reference center
Ana Cotta, Júlia Filardi Paim, Elmano Carvalho, et al.
BMC Clinical Pathology
|
October 10, 2014
Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern
Ana Cotta, Julia Filardi Paim, Antonio Lopes da-Cunha-Junior, et al.
Genes
|
May 28, 2022
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms
Ana Cotta, Lucas Santos Souza, Elmano Carvalho, et al.
Neuromuscular Disorders : NMD
|
April 9, 2021
Muscle fat replacement and modified ragged red fibers in two patients with reversible infantile respiratory chain deficiency
Ana Cotta, Elmano Carvalho, AntonioLopes da-Cunha-Junior, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 10, 2017
Phenotypic Variability of Dystrophinopathy Symptomatic Female Carriers
Ana Cotta, Julia Filardi Paim, Elmano Carvalho, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Revista Brasileira De Ortopedia
|
August 1, 2019
Limb Length Discrepancy on an 11-Month-Old Boy with Osteoid Osteoma
Ana Cotta, Renato Cesar Rezende de Castro, Julia Filardi Paim, et al.
Arquivos De Neuro-Psiquiatria
|
September 25, 2014
Common recessive limb girdle muscular dystrophies differential diagnosis: why and how?
Ana Cotta, Elmano Carvalho, Antonio Lopes da-Cunha-Júnior, et al.
Journal of Molecular Neuroscience : MN
|
August 15, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability
Ana Cotta, Julia F Paim, Elmano Carvalho, et al.
Journal of Molecular Neuroscience : MN
|
March 13, 2013
Muscle phenotypic variability in limb girdle muscular dystrophy 2 G
Julia F Paim, Ana Cotta, Antonio P Vargas, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
January 18, 2021
Dominant or recessive mutations in the <i>RYR1</i> gene causing central core myopathy in Brazilian patients
Leonardo Galleni Leão, Lucas Santos Souza, Letícia Nogueira, et al.
Arquivos De Neuro-Psiquiatria
|
December 14, 2017
The relative frequency of common neuromuscular diagnoses in a reference center
Ana Cotta, Júlia Filardi Paim, Elmano Carvalho, et al.
BMC Clinical Pathology
|
October 10, 2014
Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern
Ana Cotta, Julia Filardi Paim, Antonio Lopes da-Cunha-Junior, et al.
Genes
|
May 28, 2022
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms
Ana Cotta, Lucas Santos Souza, Elmano Carvalho, et al.
Neuromuscular Disorders : NMD
|
April 9, 2021
Muscle fat replacement and modified ragged red fibers in two patients with reversible infantile respiratory chain deficiency
Ana Cotta, Elmano Carvalho, AntonioLopes da-Cunha-Junior, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 10, 2017
Phenotypic Variability of Dystrophinopathy Symptomatic Female Carriers
Ana Cotta, Julia Filardi Paim, Elmano Carvalho, et al.
Page
of 2