Artículos por temáticas

Efficacy of approach bias modification as an add-on to smoking cessation treatment: study protocol for a randomized-controlled double-blind trial

Wittekind CE, Takano K, Sckopke P, Winkler MH, Werner GG, Ehring T, Rüther T.

Trials. 2022 Mar 21;23(1):223. doi: 10.1186/s13063-022-06155-6.

Internal carotid artery occlusion related to poorly controlled rheumatoid arthritis presenting with continuous hand shaking: A case report and literature review

Chien CF, Tsai CY, Wu MN, Lai CL, Liou LM.

Medicine (Baltimore). 2022 Mar 4;101(9):e29001. doi: 10.1097/MD.0000000000029001.

A Novel TBK1 Variant (Lys694del) Presenting With Corticobasal Syndrome in a Family With FTD-ALS Spectrum Diseases: Case Report

Seibert K, Smith H, Lapins A, Pytel P, Mastrianni JA.

Front Neurol. 2022 Mar 4;13:826676. doi: 10.3389/fneur.2022.826676. eCollection 2022.

Heterogeneity of Multiple System Atrophy: An Update

Jellinger KA.

Biomedicines. 2022 Mar 3;10(3):599. doi: 10.3390/biomedicines10030599.

Neurological manifestation of 22q11.2 deletion syndrome

Bayat M, Bayat A.

Neurol Sci. 2022 Mar;43(3):1695-1700. doi: 10.1007/s10072-021-05825-8. Epub 2022 Jan 18.

Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review

Atasu B, Acarlı ANO, Bilgic B, Baykan B, Demir E, Ozluk Y, Turkmen A, Hauser AK, Guven G, Hanagasi H, Gurvit H, Emre M, Gasser T, Lohmann E.

BMC Neurol. 2022 Mar 28;22(1):122. doi: 10.1186/s12883-022-02628-y.

PURA syndrome in a child with severe developmental delay: a challenging diagnosis

Nogueira M, Melo C, Grangeia A, Magalhães T, Soares C, Dias R, Fonseca J, Sampaio M, Sousa R.

Rev Neurol. 2022 Mar 1;74(5):170-173. doi: 10.33588/rn.7405.2021068.

Cortical myoclonus associated with coeliac disease showing a characteristic EEG pattern: A case report

Velilla-Alonso G, Martín-Miguel MDC, Massot-Tarrús A.

Seizure. 2022 Feb;95:81-83. doi: 10.1016/j.seizure.2022.01.003. Epub 2022 Jan 8.

Neuropsychiatric syndrome with myoclonus after SARS-CoV-2 infection in a paediatric patient

Della Corte M, Delehaye C, Savastano E, De Leva MF, Bernardo P, Varone A.

Clin Neurol Neurosurg. 2022 Feb;213:107121. doi: 10.1016/j.clineuro.2022.107121. Epub 2022 Jan 7.

Sporadic Creutzfeldt-Jakob disease

Salehi P, Clark M, Pinzon J, Patil A.

Am J Emerg Med. 2022 Feb;52:267.e1-267.e3. doi: 10.1016/j.ajem.2021.07.038. Epub 2021 Jul 22.

Opsoclonus-myoclonus-ataxia syndrome in children

Bhatia P, Heim J, Cornejo P, Kane L, Santiago J, Kruer MC.

J Neurol. 2022 Feb;269(2):750-757. doi: 10.1007/s00415-021-10536-3. Epub 2021 Mar 29.

Higher order visual dysfunction and myoclonic-atonic seizure: an atypical presentation of CLN6 neuronal ceroid lipofuscinosis

Mukherjee D, Bhattacharyya D, Pandit A, Dubey S.

BMJ Case Rep. 2022 Feb 9;15(2):e247790. doi: 10.1136/bcr-2021-247790.

Utility of clinical exome sequencing in progressive myoclonus epilepsy syndromes: An exploratory analysis

Jose M, Poulose P, Sundaram S, Radhakrishnan A, Nampoothiri S, Menon RN.

Clin Genet. 2022 Feb;101(2):270-271. doi: 10.1111/cge.14090. Epub 2021 Dec 9.

Progressive encephalomyelitis with rigidity and myoclonus (PERM)

Grech N, Caruana Galizia JP, Pace A.

Pract Neurol. 2022 Feb;22(1):48-50. doi: 10.1136/practneurol-2021-003087. Epub 2021 Jul 28.

It is not a simple startle but a sound-induced reflex epilepsy

Yilmaz K.

J Paediatr Child Health. 2022 Feb;58(2):340-342. doi: 10.1111/jpc.15470. Epub 2021 Mar 31.