Centro de documentación: resultados de la búsqueda

Artículo
PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway.
Autor/es:
De Winter J, Beijer D, De Ridder W, Synofzik M, Zuchner SL; PREPARE consortium, Van Damme P, Spileers W, Baets J.
Letters to the editor
Año publicación:
2021
Número de revista:
Brain vol. 144 n. 2
https://academic.oup.com/brain/article/144/2/e17/5999114
Artículo
MN1 gene loss-of-function mutation causes cleft palate in a pedigree.
Autor/es:
Shu L, He D, Wu D, Peng Y, Xi H, Mao X, Wang H.
Letters to the editor
Año publicación:
2021
Número de revista:
Brain vol. 144 n. 2
https://academic.oup.com/brain/article/144/2/e18/6044084
Artículo
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigree.
Autor/es:
Vegas N, Low K, Mak CCY, Fung JLF, Hing AV, Chung BHY, Doherty D, Amiel J, Gordon CT.
Letters to the editor
Año publicación:
2021
Número de revista:
Brain vol. 144 n. 2
https://academic.oup.com/brain/article/144/2/e19/6044085
Artículo
Reply: Reference values for the Cerebellar Cognitive Affective Syndrome Scale: age and education matter.
Autor/es:
Schmahmann JD, Vangel MG, Hoche F, Guell X, Sherman JC.
Letters to the editor
Año publicación:
2021
Número de revista:
Brain vol. 144 n. 2
https://academic.oup.com/brain/article/144/2/e20/6053682
Artículo
Early-onset phenotype of bi-allelic GRN mutations.
Autor/es:
Neuray C, Sultan T, Alvi JR, Franca MC, Assmann B, Wagner M, Canafoglia L, Franceschetti S, Rossi G, Santana I, Macario MC, Almeida MR, Kamate M, Parikh S, Elloumi HZ, Murphy D, Efthymiou S, Maroofian R, Houlden H.
Letters to the editor
Año publicación:
2021
Número de revista:
Brain vol. 144 n. 2
https://academic.oup.com/brain/article/144/2/e22/6044081
Artículo
Reply: Early-onset phenotype of bi-allelic GRN mutations.
Autor/es:
Huin V, Barbier M, Durr A, Le Ber I.
Letters to the editor
Año publicación:
2021
Número de revista:
Brain vol. 144 n. 2
https://academic.oup.com/brain/article/144/2/e23/6044082
Artículo
Correction
Corrigendum to: Biondetti E, Gaurav R, Yahia-Cherif L, Mangone G, Pyatigorskaya N, Valabrègue R, Ewenczyk C, Hutchison M, François C, Corvol JC, Vidailhet M, Lehéricy S. Spatiotemporal changes in substantia nigra neuromelanin content in Parkinson's disease . Brain. 2020 Sep 1;143(9):2757-2770. doi...
Año publicación:
2021
Número de revista:
Brain vol. 144 n. 2
https://academic.oup.com/brain/article/144/2/e24/5975182
Artículo
De-implementing Prolonged Rest Advice for Concussion in Primary Care Settings: A Pilot Stepped Wedge Cluster Randomized Trial.
Autor/es:
Silverberg ND, Otamendi T, Panenka WJ, Archambault P, Babul S, MacLellan A, Li LC; Canadian TBI Research Consortium.
Año publicación:
2021
Número de revista:
Journal of Head Trauma Rehabilitation vol. 36 n. 2
https://journals.lww.com/headtraumarehab/Fulltext/2021/03000/De_implementing_Pro…
Artículo
Clinical Detection and Recovery of Vestibular and Oculomotor Impairments Among Amateur Athletes Following Sport-Related Concussion: A Prospective, Matched-Cohort Study.
Autor/es:
Büttner F, Howell DR, Doherty C, Blake C, Ryan J, Delahunt E.
Año publicación:
2021
Número de revista:
Journal of Head Trauma Rehabilitation vol. 36 n. 2
https://journals.lww.com/headtraumarehab/Fulltext/2021/03000/Clinical_Detection_…
Artículo
Persistent Postconcussion Symptoms: An Expert Consensus-Based Definition Using the Delphi Method.
Autor/es:
Lagacé-Legendre C, Boucher V, Robert S, Tardif PA, Ouellet MC, de Guise E, Boulard G, Frémont P, Émond M, Moore L, Le Sage N.
Año publicación:
2021
Número de revista:
Journal of Head Trauma Rehabilitation vol. 36 n. 2
https://journals.lww.com/headtraumarehab/Fulltext/2021/03000/Persistent_Postconc…

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Buscador

PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway.

MN1 gene loss-of-function mutation causes cleft palate in a pedigree.

Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigree.

Reply: Reference values for the Cerebellar Cognitive Affective Syndrome Scale: age and education matter.

Early-onset phenotype of bi-allelic GRN mutations.

Reply: Early-onset phenotype of bi-allelic GRN mutations.

Correction

De-implementing Prolonged Rest Advice for Concussion in Primary Care Settings: A Pilot Stepped Wedge Cluster Randomized Trial.

Clinical Detection and Recovery of Vestibular and Oculomotor Impairments Among Amateur Athletes Following Sport-Related Concussion: A Prospective, Matched-Cohort Study.

Persistent Postconcussion Symptoms: An Expert Consensus-Based Definition Using the Delphi Method.

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