Artículos por temáticas

Pain in Parkinson's disease: new concepts in pathogenesis and treatment.

Rukavina K, Leta V, Sportelli C, et al.

Curr Opin Neurol 2019; 32:579-88.

The NRF2 Signaling Network Defines Clinical Biomarkers and Therapeutic Opportunity in Friedreich's Ataxia

La Rosa P, Bertini ES, Piemonte F.

Int J Mol Sci. 2020 Jan 30;21(3):916. doi: 10.3390/ijms21030916.

Ocular Involvement in Friedreich Ataxia Patients and its Relationship with Neurological Disability, a Follow-up Study

Rojas P, Ramírez AI, Hoz R, Cadena M, Ferreras A, Monsalve B, Salobrar-García E, Muñoz-Blanco JL, Urcelay-Segura JL, Salazar JJ, Ramírez JM.

Diagnostics (Basel). 2020 Jan 29;10(2):75. doi: 10.3390/diagnostics10020075.

Patient-Friendly Summary of the ACR Appropriateness Criteria: Ataxia

Anemone S, Vincoff NS.

J Am Coll Radiol. 2020 Apr;17(4):e15. doi: 10.1016/j.jacr.2019.12.019. Epub 2020 Jan 31.

Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8

Hosseini Bereshneh A, Hosseipour S, Rasoulinezhad MS, Pak N, Garshasbi M, Tavasoli AR.

Eur J Med Genet. 2020 May;63(5):103868. doi: 10.1016/j.ejmg.2020.103868. Epub 2020 Jan 28.

NfL and pNfH are increased in Friedreich's ataxia

Hayer SN, Liepelt I, Barro C, Wilke C, Kuhle J, Martus P, Schöls L; EFACTS study group.

J Neurol. 2020 May;267(5):1420-1430. doi: 10.1007/s00415-020-09722-6. Epub 2020 Jan 30.

Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs

Jenkins CA, Kalmar L, Matiasek K, Mari L, Kyöstilä K, Lohi H, Schofield EC, Mellersh CS, De Risio L, Ricketts SL.

PLoS Genet. 2020 Jan 30;16(1):e1008527. doi: 10.1371/journal.pgen.1008527. eCollection 2020 Jan.

Developing an objective evaluating system to quantify the degree of upper limb movement impairment in patients with severe Friedreich's ataxia

Arcuria G, Marcotulli C, Amuso R, Dattilo G, Galasso C, Pierelli F, Casali C.

Neurol Sci. 2020 Jun;41(6):1577-1587. doi: 10.1007/s10072-020-04249-0. Epub 2020 Jan 28.

miR-26a attenuates cardiac apoptosis and fibrosis by targeting ataxia-telangiectasia mutated in myocardial infarction

Chiang MH, Liang CJ, Lin LC, Yang YF, Huang CC, Chen YH, Kao HL, Chen YC, Ke SR, Lee CW, Lin MS, Chen YL.

J Cell Physiol. 2020 Sep;235(9):6085-6102. doi: 10.1002/jcp.29537. Epub 2020 Jan 28.

HIV presenting as Cerebellar Ataxia - A Case Report

Chandana GS, Jubilee M, Spj SJ.

J Assoc Physicians India. 2020 Jan;68(1):78.

A study of family members of a patient with spinocerebellar ataxia type1 (SCA 1)

Purnima P, Chandrashekar V, Rao B.

J Assoc Physicians India. 2020 Jan;68(1):67.

36 year old male with cognitive disturbance, ataxia and speech disturbances

Ts A, Nandiniswamy.

J Assoc Physicians India. 2020 Jan;68(1):66.

Methylation of the ataxia telangiectasia mutated gene (ATM) promoter as a radiotherapy outcome biomarker in patients with hepatocellular carcinoma

Yan X, Wu T, Tang M, Chen D, Huang M, Zhou S, Zhang H, Yang X, Li G.

Medicine (Baltimore). 2020 Jan;99(4):e18823. doi: 10.1097/MD.0000000000018823.

Correlation of Visual Quality of Life With Clinical and Visual Status in Friedreich Ataxia

Afsharian P, Nolan-Kenney R, Lynch AE, Balcer LJ, Lynch DR.

J Neuroophthalmol. 2020 Jun;40(2):213-217. doi: 10.1097/WNO.0000000000000878.

Thyroid Eye Disease in Hashimoto Ataxia

Kanakamedala AD, Al Othman BA, Kini AT, Lee AG.

J Neuroophthalmol. 2021 Mar 1;41(1):e83-e84. doi: 10.1097/WNO.0000000000000884.