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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.

Mioclonía y espasmos

136 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Dobutamine-Induced Myoclonus in a Peritoneal Dialysis Patient: Case Report

Noel E, Fayoda B, Rabbani R, Benjamin YS, Lee J, Gillespie A.

Kidney Med. 2022 Dec 17;5(3):100591. doi: 10.1016/j.xkme.2022.100591. eCollection 2023 Mar.

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PUBMED

Presynaptic Hemiparkinsonism Following Cerebral Toxoplasmosis: Case Report and Literature Review

Malaquias MJ, Magrinelli F, Quattrone A, Neo RJ, Latorre A, Mulroy E, Bhatia KP.

Mov Disord Clin Pract. 2022 Dec 17;10(2):285-299. doi: 10.1002/mdc3.13631. eCollection 2023 Feb.

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PUBMED

Covid-19 vaccines and neurological complications: a systematic review

Allahyari F, Molaee H, Hosseini Nejad J.

Z Naturforsch C J Biosci. 2022 Sep 12;78(1-2):1-8. doi: 10.1515/znc-2022-0092. Print 2023 Jan 27.

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PUBMED

Opsoclonus myoclonus and ataxia syndrome with supraventricular tachycardia

Garner S, Giakas A, Holder K, Galvan B, Edwards H.

Proc (Bayl Univ Med Cent). 2022 Sep 20;36(1):109-110. doi: 10.1080/08998280.2022.2123666. eCollection 2023.

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PUBMED

ADCY5 gene mutation: a case report

Tezen D, Gunduz A, Erdemir Kiziltan M, Yalcinkaya C, Kiziltan G.

Neurol Sci. 2022 Dec;43(12):6947-6950. doi: 10.1007/s10072-022-06394-0. Epub 2022 Sep 16.

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PUBMED

Towards a science-based testing strategy to identify maternal thyroid hormone imbalance and neurodevelopmental effects in the progeny-part III: how is substance-mediated thyroid hormone imbalance in pregnant/lactating rats or their progeny related to neurodevelopmental effects?

Marty MS, Sauer UG, Charlton A, Ghaffari R, Guignard D, Hallmark N, Hannas BR, Jacobi S, Marxfeld HA, Melching-Kollmuss S, Sheets LP, Urbisch D, Botham PA, van Ravenzwaay B.

Crit Rev Toxicol. 2022 Dec 15:1-72. doi: 10.1080/10408444.2022.2130166. Online ahead of print.

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PUBMED

Possible Autoimmune Encephalitis Associated with the Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant Successfully Treated with Steroids

Kato S, Yoshikura N, Kimura A, Shimohata T.

Intern Med. 2022 Dec 15;61(24):3739-3741. doi: 10.2169/internalmedicine.0371-22. Epub 2022 Oct 5.

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PUBMED

A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes

Gaweda-Walerych K, Sitek EJ, Borczyk M, Narożańska E, Brockhuis B, Korostyński M, Schinwelski M, Siemiński M, Sławek J, Zekanowski C.

Genes (Basel). 2022 Dec 14;13(12):2361. doi: 10.3390/genes13122361.

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PUBMED

Paraneoplastic Opsoclonus-Myoclonus Syndrome as a Rare Presentation of Small-Cell Lung Cancer

Moreira I, Vilas-Boas I, Cassiano Neves M.

Cureus. 2022 Nov 30;14(11):e32066. doi: 10.7759/cureus.32066. eCollection 2022 Nov.

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PUBMED

Central stress response among deprived and continuing marijuana users and nonusers

Fronk GE, Hefner K, Gloria R, Curtin JJ.

Psychol Addict Behav. 2022 Dec;36(8):1023-1035. doi: 10.1037/adb0000821. Epub 2022 Feb 24.

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PUBMED

Is the pathology of posterior cortical atrophy clinically predictable?

Cipriano L, Oliva M, Puoti G, Signoriello E, Bonavita S, Coppola C.

Rev Neurosci. 2022 Jun 6;33(8):849-858. doi: 10.1515/revneuro-2022-0003. Print 2022 Dec 16.

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PUBMED

A synthesis of deimatic behaviour

Drinkwater E, Allen WL, Endler JA, Hanlon RT, Holmes G, Homziak NT, Kang C, Leavell BC, Lehtonen J, Loeffler-Henry K, Ratcliffe JM, Rowe C, Ruxton GD, Sherratt TN, Skelhorn J, Skojec C, Smart HR, Whit

Biol Rev Camb Philos Soc. 2022 Dec;97(6):2237-2267. doi: 10.1111/brv.12891. Epub 2022 Aug 8.

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PUBMED

Creutzfeldt-Jakob disease after COVID-19: infection-induced prion protein misfolding? A case report

Bernardini A, Gigli GL, Janes F, Pellitteri G, Ciardi C, Fabris M, Valente M.

Prion. 2022 Dec;16(1):78-83. doi: 10.1080/19336896.2022.2095185.

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PUBMED

Role of SERPINI1 pathogenic variants in familial encephalopathy with neuroserpin inclusion bodies: A case report and literature review

Yang X, Fang Z, Yan L, He X, Luo H, Han Z, Gui J, Cheng M, Jiang L.

Seizure. 2022 Dec;103:137-147. doi: 10.1016/j.seizure.2022.11.008. Epub 2022 Nov 13.

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