Cargando…

Cognitive performance of children with spinal muscular atrophy: A systematic review

Spinal muscular atrophy (SMA) is genetic and progressive, caused by large bi-allelic deletions in the SMN1 gene, or the association of a large deletion and a null variant. OBJECTIVE: To evaluate the evidence about cognitive outcomes in spinal muscular atrophy (SMA). METHODS: Searches on the PUBMED/M...

Descripción completa

Detalles Bibliográficos
Autores principales:	Polido, Graziela Jorge, de Miranda, Mariana Mangini Vaz, Carvas, Nelson, Mendonça, Rodrigo de Holanda, Caromano, Fátima Aparecida, Reed, Umbertina Conti, Zanoteli, Edmar, Voos, Mariana Callil
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Associação de Neurologia Cognitiva e do Comportamento 2019
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907703/ https://www.ncbi.nlm.nih.gov/pubmed/31844498 http://dx.doi.org/10.1590/1980-57642018dn13-040011

Ejemplares similares

Air stacking: effects on pulmonary function in patients with spinal muscular atrophy and in patients with congenital muscular dystrophy,
por: Marques, Tanyse Bahia Carvalho, et al.
Publicado: (2014)

Timed immersion expiration measures in patients with muscular dystrophies
por: Voos, Mariana Callil, et al.
Publicado: (2020)

Massage and Storytelling Reduce Aggression and Improve Academic Performance in Children Attending Elementary School
por: Gonçalves, Lia Lopes, et al.
Publicado: (2017)

Balance as an Additional Effect of Strength and Flexibility Aquatic Training in Sedentary Lifestyle Elderly Women
por: Vale, Fernando Alves, et al.
Publicado: (2020)

Evaluation of muscle strength and motor abilities in children with type II and III spinal muscle atrophy treated with valproic acid
por: Darbar, Illora A, et al.
Publicado: (2011)

Lung function monitoring in patients with duchenne muscular dystrophy on steroid therapy
por: Machado, Darlene L, et al.
Publicado: (2012)

Gene therapy in neuromuscular disorders
por: Mendonça, Rodrigo Holanda, et al.
Publicado: (2022)

Responsiveness of the domain climbing up and going down stairs of the Functional Evaluation scale for Duchenne Muscular Dystrophy: a one-year follow-up
por: Albuquerque, Priscila S., et al.
Publicado: (2016)

Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy
por: Mendonça, Rodrigo de Holanda, et al.
Publicado: (2020)

Relationship between the climbing up and climbing down stairs domain scores on the FES-DMD, the score on the Vignos Scale, age and timed performance of functional activities in boys with Duchenne muscular dystrophy
por: Fernandes, Lilian A. Y., et al.
Publicado: (2014)

DNM2 mutations in a cohort of sporadic patients with centronuclear myopathy
por: Abath, Osorio, et al.
Publicado: (2015)

Hip Mobilization at Preterm Age May Accelerate Developmental Dysplasia Recovery
por: Voos, Mariana Callil, et al.
Publicado: (2018)

Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy – a Genotype/Phenotype Correlation
por: Camelo, Clara Gontijo, et al.
Publicado: (2023)

Natural history of Type 1 spinal muscular atrophy: a retrospective, global, multicenter study
por: Cances, Claude, et al.
Publicado: (2022)

Patients with Duchenne and Becker muscular dystrophies are not more asymmetrical than healthy controls on timed performance of upper limb tasks
por: Artilheiro, M.C., et al.
Publicado: (2017)

Myopathy due to HMGCR antibodies in adult mimicking muscular dystrophy associated with cancer and statin exposure – narrative review of the literature – case report
por: Carvalho, Alzira Alves de Siqueira, et al.
Publicado: (2018)

The Effects of Omega-3 Fatty Acid Supplementation on Dexamethasone-Induced Muscle Atrophy
por: Fappi, Alan, et al.
Publicado: (2014)

Gait, posture and cognition in Parkinson's disease
por: Barbosa, Alessandra Ferreira, et al.
Publicado: (2016)

Spinal muscular atrophy
por: D'Amico, Adele, et al.
Publicado: (2011)

Progressive Muscular Atrophy
por: Omar, A.
Publicado: (1947)

Progressive Muscular Atrophy
por: Omar, A.
Publicado: (1947)

Progressive Muscular Atrophy
por: Omer, M. A.
Publicado: (1949)

Muscular Atrophy and Sclerodermia
por: Nixon, J. A.
Publicado: (1903)

Progressive Muscular Atrophy
Publicado: (1874)

Muscular Atrophy and Sclerodermia
Publicado: (1904)

Acute Muscular Atrophy
por: Haddon, John
Publicado: (1870)

Case of Muscular Atrophy
por: Kersey, V.
Publicado: (1871)

Clinical Manifestation of Nebulin-Associated Nemaline Myopathy
por: Moreno, Cristiane Araujo Martins, et al.
Publicado: (2023)

Case of Marked Muscular Atrophy of Hands and Fore-Arms—Progressive Muscular Atrophy(?)
por: Ness, R. Barclay
Publicado: (1895)

A didactic approach to presenting verbal and visual information to children participating in research protocols: the comic book informed assent
por: Massetti, Thaís, et al.
Publicado: (2018)

Analysis of Different Device Interactions in a Virtual Reality Task in Individuals With Duchenne Muscular Dystrophy—A Randomized Controlled Trial
por: de Freitas, Bruna Leal, et al.
Publicado: (2019)

Improvements in motor tasks through the use of smartphone technology for individuals with Duchenne muscular dystrophy
por: Capelini, Camila Miliani, et al.
Publicado: (2017)

Nusinersen in type 0 spinal muscular atrophy: should we treat?
por: Tiberi, Eloisa, et al.
Publicado: (2020)

Pseudo-Muscular Hypertrophy and Its Relations to Muscular Atrophy
Publicado: (1875)

Omega‐3 multiple effects increasing glucocorticoid‐induced muscle atrophy: autophagic, AMPK and UPS mechanisms
por: Fappi, Alan, et al.
Publicado: (2019)

Neuronal involvement in muscular atrophy
por: Cisterna, Bruno A., et al.
Publicado: (2014)

Muscular Atrophies in Joint Disease
Publicado: (1904)

Progressive Muscular Atrophy with Recovery
por: Clarke, J. Michell
Publicado: (1888)

Muscular Atrophy in Tabes Dorsalis
Publicado: (1889)

Nusinersen for spinal muscular atrophy
por: Wurster, Claudia D., et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_r2v14q0rvqbj71fh2l819cep7b