Publicacions científiques

Stotesbury H, Kirkham FJ, Kölbel M, Balfour P, Clayden JD, Sahota S, Sakaria S, Saunders DE, Howard J, Kesse-Adu R, Inusa B, Pelidis M, Chakravorty S, Rees DC, Awogbade M, Wilkey O, Layton M, Clark CA, Kawadler JM.

Any publicació:

2018

Número de revista:

Neurology vol. 90 n. 23

http://n.neurology.org/content/90/23/e2042.abstract

Article

White matter lesions: Spatial heterogeneity, links to risk factors, cognition, genetics, and atrophy

Autor/s:

Habes M, Sotiras A, Erus G, Toledo JB, Janowitz D, Wolk DA, Shou H, Bryan NR, Doshi J, Völzke H, Schminke U, Hoffmann W, Resnick SM, Grabe HJ, Davatzikos C

Any publicació:

2018

Número de revista:

Neurology vol. 91 n.10

http://n.neurology.org/content/91/10/e964.abstract

Article

White Paper: Movement System Diagnoses in Neurologic Physical Therapy.

Autor/s:

Hedman LD, Quinn L, Gill-Body K, Brown DA, Quiben M, Riley N, Scheets PL.

Any publicació:

2018

Número de revista:

Journal of Neurologic Physical Therapy vol. 42 n. 2

https://journals.lww.com/jnpt/Fulltext/2018/04000/White_Paper___Movement_System_…

Article

Who should undergo a comprehensive cognitive assessment after a stroke? A cognitive risk score.

Autor/s:

Godefroy O, Yaïche H, Taillia H, Bompaire F, Nédélec-Ciceri C, Bonnin C, Varvat J, Vincent-Grangette F, Diouf M, Mas JL, Canaple S, Lamy C, Arnoux A, Leclercq C, Tasseel-Ponche S, Roussel M, Barbay M; GRECogVASC Study Group.

Any publicació:

2018

Número de revista:

Neurology vol. 91 n. 21

http://n.neurology.org/content/91/21/e1979.abstract

Article

Whole genome sequence analyses of brain imaging measures in the Framingham Study.

Autor/s:

Sarnowski C, Satizabal CL, DeCarli C, Pitsillides AN, Cupples LA, Vasan RS, Wilson JG, Bis JC, Fornage M, Beiser AS, DeStefano AL, Dupuis J, Seshadri S; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; TOPMed Neurocognitive Working Group.

Any publicació:

2018

Número de revista:

Neurology vol. 90 n. 3

Article

Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome.

Autor/s:

Alrohaif H, Töpf A, Evangelista T, Lek M, McArthur D, Lochmüller H.

Clinical/Scientific Notes

Any publicació:

2018

Número de revista:

Neurology® Genetics. vol. 4 n. 2

http://ng.neurology.org/content/4/2/e226.extract

Una iniciativa de:

Cercador

WHITE BOOK ON PHYSICAL AND REHABILITATION MEDICINE (PRM) IN EUROPE. EUROPEAN PHYSICAL AND REHABILITATION MEDICINE BODIES ALLIANCE. CHAPTER 6. KNOWLEDGE AND SKILLS OF PRM PHYSICIANS

White matter abnormalities and cognition in patients with conflicting diagnoses and CSF profiles.

White matter abnormalities in the corpus callosum with cognitive impairment in Parkinson disease

White matter change with apathy and impulsivity in frontotemporal lobar degeneration syndromes

White matter integrity and processing speed in sickle cell anemia.

White matter lesions: Spatial heterogeneity, links to risk factors, cognition, genetics, and atrophy

White Paper: Movement System Diagnoses in Neurologic Physical Therapy.

Who should undergo a comprehensive cognitive assessment after a stroke? A cognitive risk score.

Whole genome sequence analyses of brain imaging measures in the Framingham Study.

Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome.

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