Centre de documentació: resultats de cerca

Article
tDCS-Enhanced Consolidation of Writing Skills and Its Associations With Cortical Excitability in Parkinson Disease: A Pilot Study.
Autor/s:
Broeder S, Nackaerts E, Cuypers K, Meesen R, Verheyden G, Nieuwboer A.
Any publicació:
2019
Número de revista:
Neurorehabilitation and Neural Repair vol. 33 n. 12
https://journals.sagepub.com/doi/full/10.1177/1545968319887684
Resum de comunicació congrés
Abstracts from the 2019 Annual Meeting
Autor/s:
Meeting Abstracts
Any publicació:
2019
Número de revista:
Neurorehabilitation and Neural Repair vol. 33 n. 12
https://journals.sagepub.com/doi/full/10.1177/1545968319893871
Article
Corrigendum
Corrigendum for: Pomeroy VM, Rowe P, Clark A, Walker A, Kerr A, Chandler E, Barber M, Baron JC; SWIFT Cast Investigators. A Randomized Controlled Evaluation of the Efficacy of an Ankle-Foot Cast on Walking Recovery Early After Stroke: SWIFT Cast Trial. Neurorehabil Neural Repair. 2016 Jan;30(1):40-...
Any publicació:
2019
Número de revista:
Neurorehabilitation and Neural Repair vol. 33 n. 12
https://journals.sagepub.com/doi/full/10.1177/1545968319896700
Editorial
Headaches and polygenic scores
Autor/s:
Vilhjálmsson BJ, Privé F
Editorial
Any publicació:
2019
Número de revista:
Neurology® Genetics. vol. 5 n. 6
http://ng.neurology.org/content/5/6/e368.extract
Editorial
Rating scales for rare neurological diseases: What are we learning from Friedreich ataxia?
Autor/s:
Pandolfo M
Editorial
Any publicació:
2019
Número de revista:
Neurology® Genetics. vol. 5 n. 6
http://ng.neurology.org/content/5/6/e380.extract
Article
Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variability
Autor/s:
Barcia G, Chemaly N, Kuchenbuch M, Eisermann M, Gobin-Limballe S, Ciorna V, Macaya A, Lambert L, Dubois F, Doummar D, de Villemeur TB, Villeneuve N, Barthez MA, Nava C, Boddaert N, Kaminska A, Bahi-Buisson N, Milh M, Auvin S, Bonnefont JP, Nabbout R
Any publicació:
2019
Número de revista:
Neurology® Genetics. vol. 5 n. 6
http://ng.neurology.org/content/5/6/e363.abstract
Article
Migraine polygenic risk score associates with efficacy of migraine-specific drugs
Autor/s:
Kogelman LJA, Esserlind AL, Christensen AF, Awasthi S, Ripke S, Ingason A, Davidsson OB, Erikstrup C, Hjalgrim H, Ullum H, Olesen J, Thomas Folkmann Hansen and DBDS Genomic Consortium, The International Headache Genetics Consortium
Any publicació:
2019
Número de revista:
Neurology® Genetics. vol. 5 n. 6
http://ng.neurology.org/content/5/6/e364.abstract
Article
GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis
Autor/s:
Sliepka JM, McGriff SC, Rossetti LZ, Bizargity P, Streff H, Lee YS, Dai H, Polubothu S, Lee G, Ren V, Hunter JV, Curry DJ, Scaglia F, Adesina AM, Ali I, Kinsler V, Burrage LC, Marafi D
Any publicació:
2019
Número de revista:
Neurology® Genetics. vol. 5 n. 6
http://ng.neurology.org/content/5/6/e366.abstract
Article
Yield of comparative genomic hybridization microarray in pediatric neurology practice
Autor/s:
Misra S, Peters G, Barnes E, Ardern-Holmes S, Webster R, Troedson C, Mohammad SS, Gill D, Menezes M, Gupta S, Procopis P, Antony J, Kurian MA, Dale RC
Any publicació:
2019
Número de revista:
Neurology® Genetics. vol. 5 n. 6
http://ng.neurology.org/content/5/6/e367.abstract
Article
Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants
Autor/s:
Gauquelin L, Cayami FK, Sztriha L, Yoon G, Tran LT, Guerrero K, Hocke F, van Spaendonk RLM, Fung EL, D'Arrigo S, Vasco G, Thiffault I, Niyazov DM, Person R, Lewis KS, Wassmer E, Prescott T, Fallon P, McEntagart M, Rankin J, Webster R, Philippi H, van de Warrenburg B, Timmann D, Dixit A, Searle...
Any publicació:
2019
Número de revista:
Neurology® Genetics. vol. 5 n. 6
http://ng.neurology.org/content/5/6/e369.abstract

Una iniciativa de:

Cercador

tDCS-Enhanced Consolidation of Writing Skills and Its Associations With Cortical Excitability in Parkinson Disease: A Pilot Study.

Abstracts from the 2019 Annual Meeting

Corrigendum

Headaches and polygenic scores

Rating scales for rare neurological diseases: What are we learning from Friedreich ataxia?

Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variability

Migraine polygenic risk score associates with efficacy of migraine-specific drugs

GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis

Yield of comparative genomic hybridization microarray in pediatric neurology practice

Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants

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