Publicacions científiques | Siidon | Guttmann

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Article

Novel Associations of BST1 and LAMP3 with Rapid Eye Movement Sleep Behavior Disorder.

Autor/s:

Mufti K, Yu E, Rudakou U, Krohn L, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, Valente M, Janes F, Bernardini A, Högl B, Stefani A, Holzknecht E, Sonka K, Kemlink D, Oertel W, Janzen A, Plazzi G, Antelmi E,...

Any publicació:

2021

Número de revista:

Neurology vol. 96 n. 10

https://n.neurology.org/content/96/10/e1402

Article

Novel bifunctional hybrid compounds designed to enhance the effects of opioids and antagonize the pronociceptive effects of nonopioid peptides as potent analgesics in a rat model of neuropathic pain.

Autor/s:

Piotrowska A, Starnowska-Sokół J, Makuch W, Mika J, Witkowska E, Tymecka D, Ignaczak A, Wilenska B, Misicka A, Przewłocka B.

Any publicació:

2021

Número de revista:

Pain vol. 162 n. 2

https://journals.lww.com/pain/Fulltext/2021/02000/Novel_bifunctional_hybrid_comp…

Article

Novel Claims-Based Outcome Phenotypes in Survivors of Pediatric Traumatic Brain Injury.

Autor/s:

Maddux AB, Sevick C, Cox-Martin M, Bennett TD.

Any publicació:

2021

Número de revista:

Journal of Head Trauma Rehabilitation vol. 36 n. 4

https://journals.lww.com/headtraumarehab/Fulltext/2021/07000/Novel_Claims_Based_…

Article

Novel Cysteine-Sparing Hypomorphic NOTCH3 A1604T Mutation Observed in a Family With Migraine and White Matter Lesions.

Autor/s:

Arnardottir S, Del Gaudio F, Klironomos S, Braune EB, Lombraña AA, Oliveira DV, Jin S, Karlström H, Lendahl U, Sjöstrand C.

Any publicació:

2021

Número de revista:

Neurology® Genetics. vol. 7 n. 3

https://ng.neurology.org/content/7/3/e584

Article

Novel Mutation in the POLR1C Gene Causing Hypomyelinating Leukodystrophy in an Adult

Autor/s:

Yadav N, Saini J, Nagappa M

Cases

Any publicació:

2021

Número de revista:

Neurology® Clinical Practice vol. 11 n. 3

https://cp.neurology.org/content/11/3/e367

Article

Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy

Autor/s:

Bruhn H, Samuelsson K, Schober FA, Engvall M, Lesko N, Wibom R, Nennesmo I, Calvo-Garrido J, Press R, Stranneheim H, Freyer C, Wedell A, Wredenberg A

Any publicació:

2021

Número de revista:

Neurology® Genetics. vol. 7 n. 2

https://ng.neurology.org/content/7/2/e566

Article

Novel Mutation of the TGF-β 3 Protein (Loeys-Dietz Type 5) Associated With Aortic and Carotid Dissections: Case Report.

Autor/s:

Hussein D, Olsson C, Lagerstedt-Robinson K, Moreira T.

Clinical/Scientific Notes

Any publicació:

2021

Número de revista:

Neurology® Genetics. vol. 7 n. 6

https://ng.neurology.org/content/7/6/e625

Article

NOVEL NON‐INVASIVE STRATEGY FOR SPINAL NEUROMODULATION TO CONTROL HUMAN LOCOMOTION

Autor/s:

Moshonkina T, Grishin A, Bogacheva I, Gorodnichev R, Ovechkin A, Siu R, Edgerton VR, Gerasimenko Y.

Any publicació:

2021

https://www.frontiersin.org/articles/10.3389/fnhum.2020.622533/full

Article

Novel Score for Stratifying Risk of Critical Care Needs in Intracerebral Hemorrhage Patients: Critical Care Needs in ICH.

Autor/s:

Faigle R, Chen BJ, Krieger R, Marsh EB, Alkhachroum A, Xiong W, Urrutia VC, Gottesman RF.

Any publicació:

2021

Número de revista:

Neurology vol. 96 n. 20

https://n.neurology.org/content/96/20/e2458

Article

Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia

Autor/s:

Mol MO, Wong TH, Melhem S, Basu S, Viscusi R, Galjart N, Rozemuller AJM, Fallini C, Landers JE, Kaat LD, Seelaar H, van Rooij JGJ, van Swieten JC

Any publicació:

2021

Número de revista:

Neurology® Genetics. vol. 7 n. 3

https://ng.neurology.org/content/7/3/e596