Artículos por temáticas

Treatable Hereditary Manganese Transport Disorder: Novel SLC30A10 Mutation and its Characteristic Neuroimaging Appearance in Two Siblings

Santhakumar S, Lukas J, Unnikrishnan G, Thomas B, Kesavadas C.

J Pediatr Genet. 2020 Jul 23;10(4):305-310. doi: 10.1055/s-0040-1713853. eCollection 2021 Dec.

Biallelic Mutation of SETX and Additional Likely "In Cis" SETX Sequence Change in Ataxia with Oculomotor Apraxia Type 2

Perry MD, Evans MJ, Byrd PJ, Taylor MR.

J Pediatr Genet. 2020 Jul 20;10(4):311-314. doi: 10.1055/s-0040-1713909. eCollection 2021 Dec.

Ataxia and confusion in a 10-year-old girl

Chan CCH, Kukreti V, Inbar-Feigenberg M, Adrian-Gutierrez J.

Paediatr Child Health. 2020 May 27;26(3):137-138. doi: 10.1093/pch/pxaa058. eCollection 2021 Jun.

COVID-19 infection and stroke risk

Sadeghmousavi S, Rezaei N.

Rev Neurosci. 2020 Dec 24;32(3):341-349. doi: 10.1515/revneuro-2020-0066. Print 2021 Apr 27.

CNS implications of COVID-19: a comprehensive review

Nagu P, Parashar A, Behl T, Mehta V.

Rev Neurosci. 2020 Dec 7;32(2):219-234. doi: 10.1515/revneuro-2020-0070. Print 2021 Feb 23.

The therapeutic potential of mitochondrial transplantation for the treatment of neurodegenerative disorders

Espino De la Fuente-Muñoz C, Arias C.

Rev Neurosci. 2020 Dec 7;32(2):203-217. doi: 10.1515/revneuro-2020-0068. Print 2021 Feb 23.

Pain management programmes via video conferencing: a rapid review

Walumbe J, Belton J, Denneny D.

Scand J Pain. 2020 Oct 7;21(1):32-40. doi: 10.1515/sjpain-2020-0112. Print 2021 Jan 27.

CNS implications of COVID-19: a comprehensive review

Nagu P, Parashar A, Behl T, Mehta V.

Rev Neurosci. 2020 Dec 7;32(2):219-234. doi: 10.1515/revneuro-2020-0070. Print 2021 Feb 23.

Abnormal neurodevelopment outcome in case of neonatal hyperekplexia secondary to missense mutation in GLRB gene

Gupta NP, Verma V, Chopra S, Choudhury V.

BMJ Case Rep. 2020 Dec 15;13(12):e236152. doi: 10.1136/bcr-2020-236152.

Case Report: Overlapping Multiple Sclerosis With Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report and Review of Literature

Huang Y, Wang Q, Zeng S, Zhang Y, Zou L, Fu X, Xu Q.

Front Immunol. 2020 Dec 9;11:595417. doi: 10.3389/fimmu.2020.595417. eCollection 2020.

Clinical Spectrum of Drug-Induced Movement Disorders: A Study of 97 Patients

Gupta HV, Dhamija RK, Sharma VD.

Tremor Other Hyperkinet Mov (N Y). 2020 Dec 16;10:57. doi: 10.5334/tohm.587.

Functional and Idiopathic Cervical Dystonia in Two Family Members: A Challenging Diagnosis

Antelmi E, Conti E, Carecchio M, Tinazzi M.

Tremor Other Hyperkinet Mov (N Y). 2020 Dec 11;10:51. doi: 10.5334/tohm.558.

The "hypointense substantia nigra" sign. A novel MRI marker of progressive supranuclear palsy

Constantinides VC, Paraskevas GP, Velonakis G, Toulas P, Karavasilis E, Stefanis L, Kapaki E.

J Neurol Sci. 2020 Dec 20;421:117286. doi: 10.1016/j.jns.2020.117286. Online ahead of print.

A Novel Missense Mutation of the CSF1R Gene Causes Incurable CSF1R-Related Leukoencephalopathy: Case Report and Review of Literature

Chen J, Luo S, Li N, Li H, Han J, Ling L.

Int J Gen Med. 2020 Dec 22;13:1613-1620. doi: 10.2147/IJGM.S286421. eCollection 2020.

[Clinical experience in the treatment of motor fluctuations in Parkinson's disease. Delphi consensus of a group of experts in movement disorders]

Rodríguez-Sanz A, Peña-Llamas E, Alonso-Cánovas A, Alonso-Frech FA, Borrue-Fernández C, Catalán MJ, Fanjul-Arbós S, García-Cobos E, García-Ramos R, García Ruiz-Espiga P, Herreros-Rodríguez J, Kurtis-U

Rev Neurol. 2020 Dec 1;71(11):407-420. doi: 10.33588/rn.7111.2020088.