Publicacions científiques

Hong Y, Keylock A, Jensen B, Jacques TS, Ogunbiyi O, Omoyinmi E, Saunders D, Mallick AA, Tooley M, Newbury-Ecob R, Rankin J, Williams HJ, Ganesan V, Brogan PA, Eleftheriou D.

Any publicació:

2020

Número de revista:

Neurology® Genetics. vol. 6 n. 4

https://ng.neurology.org/content/6/4/e448

Article de revisió

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited. Genotype-phenotype correlations of all published cases

Autor/s:

Xiromerisiou G, Marogianni C, Dadouli K, Zompola C, Georgouli D, Provatas A, Theodorou A, Zervas P, Nikolaidou C, Stergiou S, Ntellas P, Sokratous M, Stathis P, Paraskevas GP, Bonakis A, Voumvourakis K, Hadjichristodoulou C, Hadjigeorgiou GM, Tsivgoulis G

Views and Reviews

Any publicació:

2020

Número de revista:

Neurology® Genetics. vol. 6 n. 3

https://ng.neurology.org/content/6/3/e434

Article

Cerebral lipogranuloma: A penetrating traumatic brain injury.

Autor/s:

Hagen M, Coras R, Engelhorn T, Schwab S, Seifert F.

NeuroImages

Any publicació:

2020

Número de revista:

Neurology vol. 95 n. 22

https://n.neurology.org/content/95/22/1019

Article

Cerebral microbleed incidence, relationship to amyloid burden: The Mayo Clinic Study of Aging

Autor/s:

Graff-Radford J, Lesnick T, Rabinstein AA, Gunter J, Aakre J, Przybelski SA, Spychalla AJ, Huston J 3rd, Brown RD Jr, Mielke MM, Lowe VJ, Knopman DS, Petersen RC, Jack CR Jr, Vemuri P, Kremers W, Kantarci K.

Any publicació:

2020

Número de revista:

Neurology vol. 94 n. 2

http://n.neurology.org/content/94/2/e190.abstract

Article

Cerebral small vessel disease due to a unique heterozygous HTRA1 mutation in an African man

Autor/s:

Oluwole OJ, Ibrahim H, Garozzo D, Ben Hamouda K, Ismail Mostafa Hassan S, Hegazy AM, Msaddi AK.

Any publicació:

2020

Número de revista:

Neurology® Genetics. vol. 6 n. 1

https://ng.neurology.org/content/6/1/e382

Editorial

Cerebral small vessel disease. Moving closer to hemodynamic function

Autor/s:

Shaaban CE, Molad J.

Any publicació:

2020

Número de revista:

Neurology vol. 94 n. 21

https://n.neurology.org/content/94/21/909

Una iniciativa de:

Cercador

Central nervous system involvement in Erdheim-Chester disease: An observational cohort study.

Central pain syndromes.

Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation.

Cerebellar White Matter Damage Is Associated With Postural Sway Deficits in People With Multiple Sclerosis.

Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited. Genotype-phenotype correlations of all published cases

Cerebral lipogranuloma: A penetrating traumatic brain injury.

Cerebral microbleed incidence, relationship to amyloid burden: The Mayo Clinic Study of Aging

Cerebral small vessel disease due to a unique heterozygous HTRA1 mutation in an African man

Cerebral small vessel disease. Moving closer to hemodynamic function

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