Artículos por temáticas

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.

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.

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.

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.

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.

Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt-Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene

Matsubayashi T, Sanjo N.

Int J Mol Sci. 2022 Dec 2;23(23):15172. doi: 10.3390/ijms232315172.

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.

Opsoclonus-myoclonus syndrome associated with pancreatic neuroendocrine tumor: a case report

Reinecke R, Reiländer A, Seiler A, Koch C, Voss M.

BMC Neurol. 2022 Dec 30;22(1):507. doi: 10.1186/s12883-022-03012-6.

A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom

Nagata T, Shinagawa S, Kobayashi N, Kondo K, Shigeta M.

Prion. 2022 Dec;16(1):7-13. doi: 10.1080/19336896.2021.2017701.

Effect of remimazolam tosilate versus etomidate on hemodynamics in patients undergoing valve replacement surgery: study protocol for a randomized controlled trial

Hu B, Zhou H, Zou X, Tan L, Song T, Zellmer L, Li X.

Trials. 2022 Dec 12;23(1):992. doi: 10.1186/s13063-022-06962-x.

Abdominal myoclonus in a patient implanted with spinal cord stimulator

Simonetta C, Bissacco J, Mercuri NB, Schirinzi T.

Neurol Sci. 2022 Dec;43(12):7001-7002. doi: 10.1007/s10072-022-06329-9. Epub 2022 Aug 15.

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.

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.

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.

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.