Publicaciones científicas

Artículo

Normalization of disrupted clock gene expression in males with tetraplegia: a crossover randomized placebo-controlled trial of melatonin supplementation

Autor/es:

Kostovski E, Frigato E, Savikj M, Dahm A, Sandset PM, Mowinckel MC, Skretting G, Østerud B, Bertolucci C, Iversen PO.

Año publicación:

2018

Número de revista:

Spinal Cord vol. 56 n. 11

https://www.nature.com/articles/s41393-018-0176-x

Resumen de comunicación congreso

North American Brain Injury Society.

Autor/es:

Silver J, Ziejewski M

North American Brain Injury Society’s Brain Injury Across the Age Spectrum: Improving Outcomes for Children, Adolescents, and Adults. Houston, Texas, on March 14—17, 2018.

Año publicación:

2018

Número de revista:

Journal of Head Trauma Rehabilitation vol. 33 n. 3

https://journals.lww.com/headtraumarehab/Citation/2018/05000/North_American_Brai…

Editorial

Not all, but specific types of cognitive complaints predict decline to MCI

Autor/es:

Jessen F, Rodriguez Née Then FS.

Editorial

Año publicación:

2018

Número de revista:

Neurology vol. 91 n. 4

http://n.neurology.org/content/91/4/153.extract

Artículo

Novel biomarker signatures for idiopathic REM sleep behavior disorder: A proteomic and system biology approach

Autor/es:

Mondello S, Kobeissy F, Mechref Y, Zhao J, Talih FR, Cosentino F, Antelmi E, Moresco M, Plazzi G, Ferri R.

Año publicación:

2018

Número de revista:

Neurology vol. 91 n.18

http://n.neurology.org/content/91/18/e1710.abstract

Artículo

Novel ELOVL4 mutation associated with erythrokeratodermia and spinocerebellar ataxia (SCA 34)

Autor/es:

Bourque PR, Warman-Chardon J, Lelli DA, LaBerge L, Kirshen C, Bradshaw SH, Hartley T, Boycott KM.

Clinical/Scientific Notes

Año publicación:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 4

http://ng.neurology.org/content/4/4/e263.extract

Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations.

Autor/es:

Hewamadduma CA, Hoggard N, O'Malley R, Robinson MK, Beauchamp NJ, Segamogaite R, Martindale J, Rodgers T, Rao G, Sarrigiannis P, Shanmugarajah P, Zis P, Sharrack B, McDermott CJ, Shaw PJ, Hadjivassiliou M...

Año publicación:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 6

http://ng.neurology.org/content/4/6/e279

Artículo

Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy

Autor/es:

Ricardo H. Roda, Brett A. McCray, Christopher J. Klein, Ahmet Hoke

Año publicación:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 1

http://ng.neurology.org/content/4/1/e220

Libro

Nuevas tecnologías en Neurorrehabilitación Aplicaciones diagnósticas y terapéuticas

Autor/es:

R Cano de la Cuerda

Año publicación:

2018

https://www.medicapanamericana.com/es-AR/libros/nuevas-tecnologias-en-neurorreha…

Artículo

Nusinersen in patients older than 7 months with spinal muscular atrophy type 1: A cohort study.

Autor/es:

Aragon-Gawinska K, Seferian AM, Daron A, Gargaun E, Vuillerot C, Cances C, Ropars J, Chouchane M, Cuppen I, Hughes I, Illingworth M, Marini-Bettolo C, Rambaud J, Taytard J, Annoussamy M, Scoto M, Gidaro T, Servais L.

Año publicación:

2018

Número de revista:

Neurology vol. 91 n.14

http://n.neurology.org/content/91/14/e1312.abstract

Artículo

Nutrients and bioactives in green leafy vegetables and cognitive decline: Prospective study.

Autor/es:

Morris MC, Wang Y, Barnes LL, Bennett DA, Dawson-Hughes B, Booth SL.

Año publicación:

2018

Número de revista:

Neurology vol. 90 n. 3

http://n.neurology.org/content/90/3/e21

Una iniciativa de:

Buscador

Normalization of disrupted clock gene expression in males with tetraplegia: a crossover randomized placebo-controlled trial of melatonin supplementation

North American Brain Injury Society.

Not all, but specific types of cognitive complaints predict decline to MCI

Novel biomarker signatures for idiopathic REM sleep behavior disorder: A proteomic and system biology approach

Novel ELOVL4 mutation associated with erythrokeratodermia and spinocerebellar ataxia (SCA 34)

Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations.

Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy

Nuevas tecnologías en Neurorrehabilitación Aplicaciones diagnósticas y terapéuticas

Nusinersen in patients older than 7 months with spinal muscular atrophy type 1: A cohort study.

Nutrients and bioactives in green leafy vegetables and cognitive decline: Prospective study.

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