Detalhe da pesquisa
1.
Solving Mendelian Mysteries: The Non-coding Genome May Hold the Key.
Cell
; 172(5): 889-891, 2018 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29474915
2.
Changes in cerebellar output abnormally modulate cortical myoclonus sensorimotor hyperexcitability.
Brain
; 147(4): 1412-1422, 2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37956080
3.
Triheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study.
Mov Disord
; 2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38725190
4.
Differential Synaptic Loss in ß-Amyloid Positive Versus ß-Amyloid Negative Corticobasal Syndrome.
Mov Disord
; 2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38671545
5.
Abnormal dopamine transporter imaging in pure autonomic failure: a potential biomarker of central nervous system involvement.
Eur J Neurol
; 31(3): e16169, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38085264
6.
EEG responses induced by cerebellar TMS at rest and during visuomotor adaptation.
Neuroimage
; 275: 120188, 2023 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37230209
7.
Reply to: "Reflecting the causes of variability of EEG responses elicited by cerebellar TMS".
Neuroimage
; 281: 120392, 2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37769927
8.
Machine Learning in Tremor Analysis: Critique and Directions.
Mov Disord
; 38(5): 717-731, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36959763
9.
Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2-1-Related Disorder.
Mov Disord
; 38(2): 347-353, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36420574
10.
A Screening Tool to Quickly Identify Movement Disorders in Patients with Inborn Errors of Metabolism.
Mov Disord
; 38(4): 646-653, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36727539
11.
Isolated Cervical Dystonia: Diagnosis and Classification.
Mov Disord
; 38(8): 1367-1378, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36989390
12.
Longitudinal Synaptic Loss in Primary Tauopathies: An In Vivo [11 C]UCB-J Positron Emission Tomography Study.
Mov Disord
; 38(7): 1316-1326, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37171832
13.
Critical care, maternal and neonatal outcomes of pregnant women with COVID-19 admitted to eight intensive care units during the wildtype, alpha and delta waves of the pandemic across the North West of England-a retrospective review.
Acta Obstet Gynecol Scand
; 102(12): 1719-1729, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37727968
14.
Globular glial tauopathy type II.
Pract Neurol
; 23(2): 153-156, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36411034
15.
Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.
Neurogenetics
; 23(2): 91-102, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35079915
16.
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.
Clin Genet
; 102(2): 98-109, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35616059
17.
Enhanced recovery after surgery recommendations for renal transplantation: guidelines.
Br J Surg
; 110(1): 57-59, 2022 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36168725
18.
A Critical Investigation of Cerebellar Associative Learning in Isolated Dystonia.
Mov Disord
; 37(6): 1187-1192, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35312111
19.
Motor Cortical Network Excitability in Parkinson's Disease.
Mov Disord
; 37(4): 734-744, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35001420
20.
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.
Mov Disord
; 37(1): 148-161, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34622992