Artículos por temáticas

An uncommon presentation of Wernicke-Korsakoff's syndrome in pregnancy: Case report

Cetera GE, D'Ambrosi F, Di Martino DD, Landi L, Criscuolo S, Caschera L, Cesano N, Ossola MW.

Radiol Case Rep. 2022 Dec 24;18(3):921-925. doi: 10.1016/j.radcr.2022.11.061. eCollection 2023 Mar.

An infant with Joubert syndrome: A case report

Tabassum S, Naeem A, Ahmad RU, Naeem F, Afzal F.

Radiol Case Rep. 2022 Dec 5;18(2):661-664. doi: 10.1016/j.radcr.2022.11.024. eCollection 2023 Feb.

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.

Spectrum of Pediatric to Early Adulthood POLR3A-Associated Movement Disorders

Zea Vera A, Bruce A, Larsh TR, Jordan Z, Brüggemann N, Westenberger A, Espay AJ, Gilbert DL, Wu SW.

Mov Disord Clin Pract. 2022 Dec 23;10(2):316-322. doi: 10.1002/mdc3.13635. 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.

Vulvar leukemia cutis: A case report and review of the literature

Saizan A, Dean OR, Scott GA, Mannava KA, Mercurio MG.

JAAD Case Rep. 2022 Nov 17;31:97-101. doi: 10.1016/j.jdcr.2022.10.039. eCollection 2023 Jan.

Prenatal diagnosis of Bardet Biedl Syndrome: A case report

Arora E, Fuks A, Meyer J, Chervenak J.

Radiol Case Rep. 2022 Nov 14;18(1):326-330. doi: 10.1016/j.radcr.2022.10.040. eCollection 2023 Jan.

Rapid-onset paraneoplastic cerebellar degeneration successfully treated by radiotherapy and tumorectomy

Westerlinck P, Janin N, Coucke P.

Int Cancer Conf J. 2022 Aug 4;12(1):19-23. doi: 10.1007/s13691-022-00569-4. eCollection 2023 Jan.

Isolated neurological presentations of mevalonate kinase deficiency

Hoytema van Konijnenburg EMM, Oussoren E, Frenkel J, van Hasselt PM.

JIMD Rep. 2022 Nov 18;64(1):53-56. doi: 10.1002/jmd2.12348. eCollection 2023 Jan.

Mild Neurological Phenotype Associated with Hypomorphic Variants in the Ataxia-Telangiectasia Mutated Gene

Caputi C, Federici G, Soddu S, Travaglini L, Piane M, Bertini E, Zanni G, Leuzzi V.

Mov Disord Clin Pract. 2022 Dec 10;10(1):124-129. doi: 10.1002/mdc3.13618. eCollection 2023 Jan.

An atypical clinical course of a 71-year-old man with right arm weakness and ataxia

Khemani P, Elliott M, Levine T.

Parkinsonism Relat Disord. 2022 Dec;105:154-156. doi: 10.1016/j.parkreldis.2022.02.010. Epub 2022 Apr 9.

Postoperative Acute-Phase Gait Training Using Hybrid Assistive Limb Improves Gait Ataxia in a Patient with Intradural Spinal Cord Compression Due to Spinal Tumors

Soma Y, Kubota S, Kadone H, Shimizu Y, Hada Y, Koda M, Sankai Y, Yamazaki M.

Medicina (Kaunas). 2022 Dec 12;58(12):1825. doi: 10.3390/medicina58121825.

A case report of Wernicke Korsakoff syndrome in a patient with cholangiocellular carcinoma: An underestimated cause of encephalopathy in cancer patients

Koca O, Demir B, Derin S, Turna ZH.

Medicine (Baltimore). 2022 Dec 2;101(48):e31904. doi: 10.1097/MD.0000000000031904.

Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L-Associated Neuropathy

Eggermann K, Meyer R, Begemann M, Dey D, Bültmann E, Kurth I, Korenke GC, Knopp C.

Genes (Basel). 2022 Dec 14;13(12):2356. doi: 10.3390/genes13122356.

An atypical course of a 71-year old man with right arm weakness and ataxia: Expert commentary

Mohamed Ibrahim N.

Parkinsonism Relat Disord. 2022 Dec;105:157-158. doi: 10.1016/j.parkreldis.2022.10.015. Epub 2022 Oct 18.