Inicia sesión Registrate Mi Biblioteca idioma

Idioma

biblioteca idioma abrir menu

Bibliografía Científica

Artículos por temáticas

En este apartado encontrará la selección de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por International Parkinson & Movement Disorder Society.

Ataxia

395 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

A rare central nervous system tumor of childhood with spongiform appearance on brain magnetic resonance imaging; primary diffuse leptomeningeal oligodendrogliomatosis

Tekin HG, Karaoğlu P, Bolat E.

Neurocirugia (Astur : Engl Ed). 2022 Jul-Aug;33(4):190-194. doi: 10.1016/j.neucie.2020.12.007.

0

0

0

PUBMED

A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndrome

Komatsu K, Fukumura S, Minagawa K, Nakashima M, Saitsu H.

Brain Dev. 2022 Aug;44(7):474-479. doi: 10.1016/j.braindev.2022.03.008. Epub 2022 Apr 7.

0

0

0

PUBMED

Disseminated Mycobacterium avium infection in a cat on long-term ciclosporin therapy and potential latent infection of an in-contact cat

Webster J, Marchesi F, Gunn-Moore D, Haining H, Ridyard AE.

JFMS Open Rep. 2022 Aug 10;8(2):20551169221109442. doi: 10.1177/20551169221109442. eCollection 2022 Jul-Dec.

0

0

0

PUBMED

Diagnosis of spinal dural defect using three-dimensional fast steady-state MR in patient with superficial siderosis: A case report

Sano N, Kawauchi T, Yanagida N, Torikoshi S, Ikeda H, Okoshi T, Hayase M, Nishimura M, Toda H.

Surg Neurol Int. 2022 Jul 8;13:296. doi: 10.25259/SNI_531_2022. eCollection 2022.

0

0

0

PUBMED

COVID-19 Presenting As Miller Fisher Syndrome in a Patient With a History of Guillain-Barré Syndrome: A Case Report

Aldabain L, Haddaden M, Farooqi R, Alissa M.

Cureus. 2022 Jul 5;14(7):e26588. doi: 10.7759/cureus.26588. eCollection 2022 Jul.

0

0

0

PUBMED

Cerebrotendinous xanthomatosis: clinical and imaging clues of a rare treatable cause of ataxia

Magriço M, Cabral P, Bugalho P.

BMJ Case Rep. 2022 Jul 20;15(7):e250714. doi: 10.1136/bcr-2022-250714.

0

0

0

PUBMED

Case report: A pediatric case of Bickerstaff brainstem encephalitis after COVID-19 vaccination and Mycoplasma pneumoniae infection: Looking for the culprit

Monte G, Pro S, Ursitti F, Ferilli MAN, Moavero R, Papetti L, Sforza G, Bracaglia G, Vigevano F, Palma P, Valeriani M.

Front Immunol. 2022 Aug 12;13:987968. doi: 10.3389/fimmu.2022.987968. eCollection 2022.

0

0

0

PUBMED

First report of novel mutation (c.790del) on SQSTM1 gene on a family with childhood onset of progressive cerebellar ataxia with vertical gaze palsy

Jalali H, Khoshaeen A, Mahdavi MR, Mahdavi M.

Clin Case Rep. 2022 Aug 9;10(8):e6203. doi: 10.1002/ccr3.6203. eCollection 2022 Aug.

0

0

0

PUBMED

CLN8 Gene Compound Heterozygous Variants: A New Case and Protein Bioinformatics Analyses

Sharkia R, Zalan A, Zahalka H, Kessel A, Asaly A, Al-Shareef W, Mahajnah M.

Genes (Basel). 2022 Aug 5;13(8):1393. doi: 10.3390/genes13081393.

0

0

0

PUBMED

Case Report: Evidences of myasthenia and cerebellar atrophy in a chinese patient with novel compound heterozygous MSTO1 variants

Liu L, Su R, Huang P, Li X, Xiong J, Xiao Y, Mao D, Liu L.

Front Genet. 2022 Aug 11;13:947886. doi: 10.3389/fgene.2022.947886. eCollection 2022.

0

0

0

PUBMED

Homozygous ATM mutation due to germline uniparental isodisomy in patient with T acute lymphoblastic leukemia and hepatosplenic T-cell lymphoma

Jacobs MF, Robinson D, Wu YM, Opipari VP, Mody R.

Cancer Genet. 2022 Aug;266-267:15-18. doi: 10.1016/j.cancergen.2022.05.039. Epub 2022 May 21.

0

0

0

PUBMED

Regenerative Radio Electric Asymmetric Conveyer Treatment in Generalized Cerebral and Cerebellar Atrophy to Improve Motor Control: A Case Report

Rinaldi S, Rinaldi C, Fontani V.

Cureus. 2022 Aug 21;14(8):e28245. doi: 10.7759/cureus.28245. eCollection 2022 Aug.

0

0

0

PUBMED

A Comparison of Pathogenic Eukaryotic Elongation Factor 2 (EEF2) Variants in Spinocerebellar Ataxia 26 Versus De Novo Mutations

Zhao H, Mata-Machado N.

Cureus. 2022 Jul 14;14(7):e26857. doi: 10.7759/cureus.26857. eCollection 2022 Jul.

0

0

0

PUBMED

Anti-dipeptidyl-peptidase-like protein 6 encephalitis with pure cerebellar ataxia: a case report

Lin J, Zhu M, Mao X, Jin Z, Zhou M, Hong D.

BMC Neurol. 2022 Jul 1;22(1):242. doi: 10.1186/s12883-022-02769-0.

0

0

0

PUBMED

An open-label pilot study of recombinant granulocyte-colony stimulating factor in Friedreich's ataxia

Kemp KC, Georgievskaya A, Hares K, Redondo J, Bailey S, Rice CM, Scolding NJ, Metcalfe C, Wilkins A.

Nat Commun. 2022 Aug 9;13(1):4655. doi: 10.1038/s41467-022-31450-w.

0

0

0

Comentarios

En ningún caso la información facilitada constituye asesoramiento por parte de Zambon

Con el aval de:

Logo SEN Logo HONcode Logo WIS

En colaboración con:

Zambon Neuroacademy