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Bibliografía Científica

Artículos por temáticas

En este apartado encontrará una actualización mensual de artículos sobre la enfermedad de Alzheimer/demencias y sobre los Trastornos del Movimiento clasificados según los 11 tipos establecidos por la International Parkinson & Movement Disorder Society.

173896 ARTíCULOS , VIENDO DEL 173401 AL 173415

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Reply: Not every excessive startle is hyperekplexia, the curious case of SOD1

Park JH, Elpers C, Marquardt T.

Brain. 2020 Feb 1;143(2):e12. doi: 10.1093/brain/awz416.

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Not every excessive startle is hyperekplexia, the curious case of SOD1

van der Veen S, de Vries JJ, Tijssen MAJ.

Brain. 2020 Feb 1;143(2):e11. doi: 10.1093/brain/awz415.

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Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction

Panneman DM, Wortmann SB, Haaxma CA, van Hasselt PM, Wolf NI, Hendriks Y, Küsters B, van Emst-de Vries S, van de Westerlo E, Koopman WJH, Wintjes L, van den Brandt F, de Vries M, Lefeber DJ, Smeitink

Clin Genet. 2020 Apr;97(4):556-566. doi: 10.1111/cge.13706. Epub 2020 Jan 30.

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Teaching Video NeuroImages: Palatal myoclonus in leukodystrophies: A clinical sign orienting to Alexander disease

Martinez-Poles J, Escribano-Paredes JB, García-Madrona S, Nedkova-Hristova V, Jiménez-Escrig A.

Neurology. 2020 Jan 14;94(2):e230-e231. doi: 10.1212/WNL.0000000000008795.

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Palatal myoclonus, abnormal eye movements, and olivary hypertrophy in GAD65-related disorder

Macaron G, Willis MA, Ontaneda D, Fernandez H, Kim S, Jones SE, Pioro EP, Cohen JA.

Neurology. 2020 Feb 11;94(6):273-275. doi: 10.1212/WNL.0000000000008926. Epub 2019 Dec 31.

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Lyme neuroborreliosis presenting as spinal myoclonus.

Li X, Kirschner A, Metrie M, Loeb M.

BMJ Case Rep. 2019 Dec 29;12(12). pii: e233162. doi: 10.1136/bcr-2019-233162.

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Alterations in brainstem auditory processing, the acoustic startle response and sensorimotor gating of startle in Wistar audiogenic rats (WAR), an animal model of reflex epilepsies.

Cunha AOS, Moradi M, de Deus JL, Ceballos CC, Benites NM, de Barcellos Filho PCG, de Oliveira JAC, Garcia-Cairasco N, Leão R.

Brain Res. 2020 Jan 15;1727:146570. doi: 10.1016/j.brainres.2019.146570. Epub 2019 Dec 5.

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Alpha(2)-adrenergic dysregulation in congenic DxH recombinant inbred mice selectively bred for a high fear-sensitized (H-FSS) startle response.

Wickramasekara RN, Bockman C, Hanke J, Schwegler H, McGee J, Walsh E, Yilmazer-Hanke D.

Pharmacol Biochem Behav. 2020 Jan;188:172835. doi: 10.1016/j.pbb.2019.172835. Epub 2019 Dec 2.

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Knee Buckling (Negative Myoclonus) Associated With Clozapine: Reports on 3 Cases.

Uzun Ö, Bolu A, Taşçi AB, Oğur B.

Clin Neuropharmacol. 2020 Jan/Feb;43(1):26-27. doi: 10.1097/WNF.0000000000000370.

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Interpersonal trauma exposure and startle reactivity to uncertain threat in individuals with alcohol use disorder.

Gorka SM.

Drug Alcohol Depend. 2020 Jan 1;206:107727. doi: 10.1016/j.drugalcdep.2019.107727. Epub 2019 Nov 6.

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Muscimol injection into the substantia nigra but not globus pallidus affects prepulse inhibition and startle reflex.

Rodrigues S, Ferreira TL.

Neuropharmacology. 2020 Jan 1;162:107796. doi: 10.1016/j.neuropharm.2019.107796. Epub 2019 Sep 26.

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Psychophysiological treatment outcomes: Corticotropin-releasing factor type 1 receptor antagonist increases inhibition of fear-potentiated startle in PTSD patients.

Jovanovic T, Duncan EJ, Kaye J, Garza K, Norrholm SD, Inslicht SS, Neylan TC, Mathew SJ, Iosifescu D, Rothbaum BO, Mayberg HS, Dunlop BW.

Psychophysiology. 2020 Jan;57(1):e13356. doi: 10.1111/psyp.13356. Epub 2019 Feb 26.

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Treatment-refractory paraneoplastic opsoclonus-myoclonus syndrome in a patient with small-cell carcinoma of the lung.

Alkan A, Cenikli U, Uylaş S, Yılmaz M, Çakır T, Çetinkaya H, Kıran A, Tanrıverdi Ö.

J Oncol Pharm Pract. 2020 Jan;26(1):209-211. doi: 10.1177/1078155219831366. Epub 2019 Feb 22. Erratum in: J Oncol Pharm Pract. 2019 Jun;25(4):NP4.

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Myoclonus

Ibrahim W, Zafar N, Sharma S.

2021 Aug 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan–.

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Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy

AlMuhaizea M, AlMass R, AlHargan A, AlBader A, Medico Salsench E, Howaidi J, Ihinger J, Karachunski P, Begtrup A, Segura Castell M, Bauer P, Bertoli-Avella A, Kaya IH, AlSufayan J, AlQuait L, Chedrawi

Acta Neuropathol. 2020 Apr;139(4):791-794. doi: 10.1007/s00401-020-02128-8. Epub 2020 Jan 31.

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