Publicacions científiques

Pulit SL, Weng LC, McArdle PK, Trinquart L, Choi SH, Mitchell BD, Rosand J, de Bakker PIW, Benjamin EJ, Ellinor PT, Kittner SJ, Lubitz SA, Anderson CD

Any publicació:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 6

http://ng.neurology.org/content/4/6/e293.abstract

Article

Atrial fibrillation, antithrombotic treatment, and cognitive aging: A population-based study.

Autor/s:

Ding M, Fratiglioni L, Johnell K, Santoni G, Fastbom J, Ljungman P, Marengoni A, Qiu C.

Any publicació:

2018

Número de revista:

Neurology vol. 91 n. 19

http://n.neurology.org/content/91/19/e1732

Article

Atrophy patterns in cerebral amyloid angiopathy with and without cortical superficial siderosis

Autor/s:

Kim J, Na HK, Shin JH, Kim HJ, Seo SW, Seong JK, Na DL.

Any publicació:

2018

Número de revista:

Neurology vol. 90 n. 20

http://n.neurology.org/content/90/20/e1751.abstract

Article

Attention-deficit/hyperactivity disorder medication and seizures

Autor/s:

Wiggs KK, Chang Z, Quinn PD, Hur K, Gibbons R, Dunn D, Brikell I, Larsson H, D'Onofrio BM...

Any publicació:

2018

Número de revista:

Neurology vol. 90 n. 13

http://n.neurology.org/content/90/13/e1104.abstract

Article

Attentional dysfunction and recovery in concussion: effects on the P300m and contingent magnetic variation.

Autor/s:

Petley L, Bardouille T, Chiasson D, Froese P, Patterson S, Newman A, Omisade A, Beyea S.

Any publicació:

2018

Número de revista:

Brain Injury vol. 32 n. 4

http://www.tandfonline.com/doi/full/10.1080/02699052.2018.1429022

Article

Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma

Autor/s:

Machol K, Jankovic J, Vijayakumar D, Burrage LC, Jain M, Lewis RA, Fuller GN, Xu M, Penas-Prado M, Gule-Monroe MK, Rosenfeld JA, Chen R, Eng CM, Yang Y, Lee BH, Moretti PM; Undiagnosed Diseases Network, Dhar SU.

Clinical/Scientific Notes

Any publicació:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 4

http://ng.neurology.org/content/4/4/e248.extract

Article

Atypical periodic paralysis and myalgia: A novel RYR1 phenotype.

Autor/s:

Matthews E, Neuwirth C, Jaffer F, Scalco RS, Fialho D, Parton M, Raja Rayan D, Suetterlin K, Sud R, Spiegel R, Mein R, Houlden H, Schaefer A, Healy E, Palace J, Quinlivan R, Treves S, Holton JL, Jungbluth H, Hanna MG.

Any publicació:

2018

Número de revista:

Neurology vol. 90 n. 5

http://n.neurology.org/content/90/5/e412

Una iniciativa de:

Cercador

Asymmetric TDP pathology in primary progressive aphasia with right hemisphere language dominance.

Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant

Ataxia-telangiectasia: A new remitting form with a peculiar transcriptome signature.

Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

Atrial fibrillation, antithrombotic treatment, and cognitive aging: A population-based study.

Atrophy patterns in cerebral amyloid angiopathy with and without cortical superficial siderosis

Attention-deficit/hyperactivity disorder medication and seizures

Attentional dysfunction and recovery in concussion: effects on the P300m and contingent magnetic variation.

Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma

Atypical periodic paralysis and myalgia: A novel RYR1 phenotype.

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