Publicacions científiques

Uniken Venema SM, Wolff L, van den Berg SA, Reinink H, Luijten SPR, Lingsma HF, Marquering HA, Boers AMM, Bot J, Hammer S, Nederkoorn PJ, Roos YBWEM, Majoie CBLM, Dankbaar JW, van der Lugt A, van der Worp HB; MR CLEAN Registry Investigators.

Any publicació:

2022

Número de revista:

Neurology vol. 99 n. 15

https://n.neurology.org/content/99/15/e1609

Article de revisió

TIME TO RECONCILE RESEARCH FINDINGS AND CLINICAL PRACTICE ON UPPER LIMB NEUROREHABILITATION

Autor/s:

Boccuni L, Marinelli L, Trompetto C, Pascual-Leone A, Tormos Muñoz JM.

Any publicació:

2022

https://www.frontiersin.org/articles/10.3389/fneur.2022.939748/full

Article de revisió

TIME TO RECONCILE RESEARCH FINDINGS AND CLINICAL PRACTICE ON UPPER LIMB NEUROREHABILITATION

Autor/s:

Boccuni L, Marinelli L, Trompetto C, Pascual-Leone A, Tormos Muñoz JM.

Any publicació:

2022

https://www.frontiersin.org/articles/10.3389/fneur.2022.939748/full

Comentari

Time vs mechanism in chronic pain.

Autor/s:

Nicholas MK

Commentary

Any publicació:

2022

Número de revista:

Pain vol. 163 n. 9

https://journals.lww.com/pain/Fulltext/2022/09000/Time_vs_mechanism_in_chronic_p…

Article

Timing of SARS-CoV-2 Vaccination Matters in People With Multiple Sclerosis on Pulsed Anti-CD20 Treatment.

Autor/s:

Woopen C, Dunsche M, Haase R, Raposo C, Pedotti R, Akgün K, Ziemssen T.

Any publicació:

2022

Número de revista:

Neurology Neuroimmunology & Neuroinflammation vol. 9 n. 6

https://nn.neurology.org/content/9/6/e200031

Article

TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.

Autor/s:

Tábara LC, Al-Salmi F, Maroofian R, Al-Futaisi AM, Al-Murshedi F, Kennedy J, Day JO, Courtin T, Al-Khayat A, Galedari H, Mazaheri N, Protasoni M, Johnson M, Leslie JS, Salter CG, Rawlins LE, Fasham J, Al-Maawali A, Voutsina N, Charles P, Harrold L, Keren B, Kunji ERS, Vona B, Jelodar G, Sedaghat A...

Any publicació:

2022

Número de revista:

Brain vol. 145 n. 9

https://academic.oup.com/brain/article/145/9/3095/6610907

TNNI1 Mutated in Autosomal Dominant Proximal Arthrogryposis.

Autor/s:

Nishimori Y, Iida A, Ogasawara M, Okubo M, Yonenobu Y, Kinoshita M, Sugie K, Noguchi S, Nishino I.

Clinical/Scientific Notes

Any publicació:

2022

Número de revista:

Neurology® Genetics. vol. 8 n. 1

https://ng.neurology.org/content/8/1/e649

Una iniciativa de:

Cercador

Time Course for Benefit and Risk of Ticagrelor and Aspirin in Acute Ischemic Stroke or Transient Ischemic Attack.

Time course prevalence of post-COVID pain symptoms of musculoskeletal origin in patients who had survived to severe acute respiratory syndrome coronavirus 2 infection: a systematic review and meta-analysis.

Time Since Lower-Limb Amputation: An Important Consideration in Mobility Outcomes.

Time Since Stroke Onset, Quantitative Collateral Score, and Functional Outcome After Endovascular Treatment for Acute Ischemic Stroke.

TIME TO RECONCILE RESEARCH FINDINGS AND CLINICAL PRACTICE ON UPPER LIMB NEUROREHABILITATION

TIME TO RECONCILE RESEARCH FINDINGS AND CLINICAL PRACTICE ON UPPER LIMB NEUROREHABILITATION

Time vs mechanism in chronic pain.

Timing of SARS-CoV-2 Vaccination Matters in People With Multiple Sclerosis on Pulsed Anti-CD20 Treatment.

TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.

TNNI1 Mutated in Autosomal Dominant Proximal Arthrogryposis.

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