Publicaciones científicas

Baunsgaard CB, Nissen UV, Brust AK, Frotzler A, Ribeill C, Kalke YB, León N, Gómez B, Samuelsson K, Antepohl W, Holmström U, Marklund N, Glott T, Opheim A, Penalva JB, Murillo N, Nachtegaal J, Faber W, Biering-Sørensen F

Año publicación:

2018

https://www.medicaljournals.se/jrm/content/abstract/10.2340/16501977-2372

Artículo de revisión

Exosomes and Their MicroRNA Cargo: New Players in Peripheral Nerve Regeneration.

Autor/es:

Qing L, Chen H, Tang J, Jia X.

Review

Año publicación:

2018

Número de revista:

Neurorehabilitation and Neural Repair vol. 32 n. 9

http://journals.sagepub.com/doi/full/10.1177/1545968318798955

Artículo

Expanded autologous regulatory T-lymphocyte infusions in ALS: A phase I, first-in-human study.

Autor/es:

Thonhoff JR, Beers DR, Zhao W, Pleitez M, Simpson EP, Berry JD, Cudkowicz ME, Appel SH

Año publicación:

2018

Número de revista:

Neurology Neuroimmunology & Neuroinflammation vol. 5 n. 4

http://nn.neurology.org/content/5/4/e465

Comentario

Expanding incentives for coordinated, patient-centered care: Implications for neurologists.

Autor/es:

Mantyh WG, Cohen BH, Ciccarelli L, Philpot L, Jones L

Año publicación:

2018

Número de revista:

Neurology® Clinical Practice vol. 8 n. 1

http://cp.neurology.org/content/8/1/62

Artículo

Expanding the ADCY5 phenotype toward spastic paraparesis A mutation in the M2 domain

Autor/es:

Anne J.E. Waalkens, Fleur Vansenne, Annemarie H. van der Hout, Rodi Zutt, Jeroen Mourmans, Eduardo Tolosa, Tom J. de Koning, Marina A.J. Tijssen

Clinical/Scientific Notes

Año publicación:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 1

http://ng.neurology.org/content/4/1/e214

Artículo

Expanding the global prevalence of spinocerebellar ataxia type 42.

Autor/es:

Ngo K, Aker M, Petty LE, Chen J, Cavalcanti F, Nelson AB, Hassin-Baer S, Geschwind MD, Perlman S, Italiano D, Laganà A, Cavallaro S, Coppola G, Below JE, Fogel BL.

Erratum in: Neurol Genet. 2018 May 18;4(3):e238.

Año publicación:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 3

http://ng.neurology.org/content/4/3/e232

Artículo

Expanding the phenotype of de novo SLC25A4-linked mitochondrial disease to include mild myopathy

Autor/es:

King MS, Thompson K, Hopton S, He L, Kunji ERS, Taylor RW, Ortiz-Gonzalez XR.

Año publicación:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 4

http://ng.neurology.org/content/4/4/e256.abstract

Una iniciativa de:

Buscador

Exercise Therapy for Low Back Pain: A Systematic Review.

Exercise Therapy in Juvenile Idiopathic Arthritis: A Systematic Review and Meta-Analysis.

Exertional Tolerance Assessments After Mild Traumatic Brain Injury: A Systematic Review.

EXOSKELETON GAIT TRAINING AFTER SPINAL CORD INJURY: AN EXPLORATORY STUDY ON SECONDARY HEALTH CONDITIONS

Exosomes and Their MicroRNA Cargo: New Players in Peripheral Nerve Regeneration.

Expanded autologous regulatory T-lymphocyte infusions in ALS: A phase I, first-in-human study.

Expanding incentives for coordinated, patient-centered care: Implications for neurologists.

Expanding the ADCY5 phenotype toward spastic paraparesis A mutation in the M2 domain

Expanding the global prevalence of spinocerebellar ataxia type 42.

Expanding the phenotype of de novo SLC25A4-linked mitochondrial disease to include mild myopathy

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