Artículos por temáticas

Subacute tremor and ataxia: Diligence in pursuit of a diagnosis: Expert commentary

Reich SG.

Parkinsonism Relat Disord. 2022 Nov;104:132-133. doi: 10.1016/j.parkreldis.2022.10.018. Epub 2022 Oct 30.

Superficial intraventricular surface siderosis brain

Harizi E, Shemsi K, Ahmetgjekaj I, Parisapogu A, Mamillo K, Hyseni F, Lahori S, Prathima K, Banavath CN, Syed Z, Pichuthirumalai S, Musa J, Saini J, Alidema AH, Vokshi V, Siddique MA.

Radiol Case Rep. 2022 Sep 6;17(11):4152-4155. doi: 10.1016/j.radcr.2022.08.022. eCollection 2022 Nov.

Ocular Cyclopentolate: A Mini Review Concerning Its Benefits and Risks

Contreras-Salinas H, Orozco-Ceja V, Romero-López MS, Barajas-Virgen MY, Baiza-Durán LM, Rodríguez-Herrera LY.

Clin Ophthalmol. 2022 Nov 15;16:3753-3762. doi: 10.2147/OPTH.S388982. eCollection 2022.

Pluripotent stem cell strategies for rebuilding the human brain

Limone F, Klim JR, Mordes DA.

Front Aging Neurosci. 2022 Nov 2;14:1017299. doi: 10.3389/fnagi.2022.1017299. eCollection 2022.

ACR Appropriateness Criteria® Ataxia-Child

Expert Panel on Pediatric Imaging, Radhakrishnan R, Shea LAG, Pruthi S, Silvera VM, Bosemani T, Desai NK, Gilbert DL, Glenn OA, Guimaraes CV, Ho ML, Lam HFS, Maheshwari M, Mirsky DM, Nadel HR, Partap

J Am Coll Radiol. 2022 Nov;19(11S):S240-S255. doi: 10.1016/j.jacr.2022.09.010.

Chemopreventive and therapeutic properties of anthocyanins in breast cancer: A comprehensive review

Li W, Peng C, Zhaojie L, Wei W.

Nutr Res. 2022 Nov;107:48-64. doi: 10.1016/j.nutres.2022.08.005. Epub 2022 Sep 2.

Neuropsychological assessment of Boucher-Neuhäuser syndrome: A case report

Merolla S, Borella M, Bassi F, Canonico F, Santilli IM, Grassi MP.

Clin Neuropsychol. 2022 Nov;36(8):2370-2378. doi: 10.1080/13854046.2021.1965219. Epub 2021 Aug 29.

[Peripheral Neuropathy in RFC1 CANVAS/Spectrum Disorders]

Osaki Y, Izumi Y.

Brain Nerve. 2022 Nov;74(11):1281-1286. doi: 10.11477/mf.1416202228.

Successful Haploidentical Bone Marrow Transplantation of an Infant With a Novel Mutation in SAMD9L Gene (Ataxia-Pancytopenia Syndrome)

Alicea Marrero MM, Español M, Marrero-Rivera G, Bauchat A, Cruz V, Yu L, LeBlanc Z.

J Pediatr Hematol Oncol. 2022 Oct 1;44(7):419-420. doi: 10.1097/MPH.0000000000002537. Epub 2022 Sep 2.

Bilateral hypertrophic olivary degeneration in a syndrome of sensory ataxic neuropathy with dysarthria and ophthalmoplegia

Aldendail CF, Caress JB.

Muscle Nerve. 2022 Oct;66(4):E15-E18. doi: 10.1002/mus.27689. Epub 2022 Aug 15.

Can plasma exchange therapy be an option for the treatment of SARS-CoV-2 Related Splenial Lesion Syndrome: Two cases from the pediatric intensive care unit

Varol F, Ergul N, Sahin EG, Can YY, Ergul U, Guven S, Cam H.

Transfus Apher Sci. 2022 Oct;61(5):103491. doi: 10.1016/j.transci.2022.103491. Epub 2022 Jun 11.

A PMM2-CDG caused by an A108V mutation associated with a heterozygous 70 kilobases deletion case report

Lebredonchel E, Riquet A, Neut D, Broly F, Matthijs G, Klein A, Foulquier F.

Ital J Pediatr. 2022 Oct 11;48(1):178. doi: 10.1186/s13052-022-01355-x.

Two-year follow-up of docosahexaenoic acid supplementation in spinocerebellar ataxia type 38 (SCA38)

Gazulla J, Benavente I, García-González E, Berciano J.

J Neurol. 2022 Oct;269(10):5643-5646. doi: 10.1007/s00415-022-11138-3. Epub 2022 Apr 19.

A novel homozygous missense variant in the NAXE gene in an Iranian family with progressive encephalopathy with brain edema and leukoencephalopathy

Mohammadi P, Heidari M, Ashrafi MR, Mahdieh N, Garshasbi M.

Acta Neurol Belg. 2022 Oct;122(5):1201-1210. doi: 10.1007/s13760-021-01717-y. Epub 2021 Jun 13.

Bringing light into the darkness: autosomal recessive cerebellar ataxia due to a recessive mutation in the SEPSECS gene

Martínez-Martín Á, García-García J, Díaz-Maroto Cicuéndez I, Quintanilla-Mata ML, Segura T.

Neurologia (Engl Ed). 2022 Oct;37(8):709-710. doi: 10.1016/j.nrleng.2022.01.002. Epub 2022 May 28.