Search Results - "Toft, Mathias"

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Subthalamic Nucleus Stimulation in Parkinson's Disease: 5‐Year Extension Study of a Randomized Trial.

Authors: Bjerknes, Silje Toft, Mathias Brandt, Reidun et al.

Source: Movement Disorders Clinical Practice. Jan2022, Vol. 9 Issue 1, p48-59. 12p.

Pleiotropy with sex-specific traits reveals genetic aspects of sex differences in Parkinson's disease.

Authors: Nordengen, Kaja Cappelletti, Chiara Bahrami, Shahram et al.

Source: Brain: A Journal of Neurology; Mar2024, Vol. 147 Issue 3, p858-870, 13p

Dopamine agonist serum concentrations and impulse control disorders in Parkinson's disease.

Authors: Staubo, Sara C. Fuskevåg, Ole Martin Toft, Mathias et al.

Source: European Journal of Neurology. Feb2024, Vol. 31 Issue 2, p1-9. 9p.

Subjects: Impulse control disorders, Parkinson's disease, Dopamine agonists, Drug monitoring, Compulsive shopping

Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease.

Authors: Tunold, Jon-Anders Tan, Manuela M X Koga, Shunsuke et al.

Source: Brain: A Journal of Neurology; Oct2023, Vol. 146 Issue 10, p4077-4087, 11p

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Multiple Microelectrode Recordings in STN‐DBS Surgery for Parkinson's Disease: A Randomized Study.

Authors: Bjerknes, Silje Toft, Mathias Konglund, Ane E. et al.

Source: Movement Disorders Clinical Practice. May2018, Vol. 5 Issue 3, p296-305. 10p.

New gene involved in the pathogenesis of Parkinson's disease.

Authors: Toft, Mathias^1,2 (AUTHOR) mathias.toft@medisin.uio.no

Source: Lancet Neurology. Jun2024, Vol. 23 Issue 6, p550-552. 3p.

Aggravated stuttering following subthalamic deep brain stimulation in Parkinson's disease - two cases.

Authors: Toft, Mathias Dietrichs, Espen

Source: BMC Neurology. 2011, Vol. 11 Issue 1, p44-47. 4p.

Fine-mapping and candidate gene investigation within the PARK10 locus.

Authors: Haugarvoll, Kristoffer Toft, Mathias Skipper, Lisa et al.

Source: European Journal of Human Genetics. Mar2009, Vol. 17 Issue 3, p336-343. 8p. 2 Diagrams, 2 Charts, 1 Graph.

Pupil-light reflex in early-stage Parkinson's disease.

Authors: Dalbro, Solveig EJ Pihlstrøm, Lasse Kerty, Emilia et al.

Source: Journal of Parkinson's Disease. Jun2026, Vol. 16 Issue 4, p803-805. 3p.

Impulse control and correlation to dopamine agonist serum concentrations in people with Parkinson's disease.

Authors: Staubo, Sara C. Fuskevåg, Ole Martin Toft, Mathias et al.

Source: Journal of Neurology. Feb2025, Vol. 272 Issue 2, p1-12. 12p.

Long-term efficacy and mortality in Parkinson's disease patients treated with subthalamic stimulation.

Authors: Toft, Mathias Lilleeng, Bård Ramm-Pettersen, Jon et al.

Source: Movement Disorders. Aug2011, Vol. 26 Issue 10, p1931-1934. 4p.

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.

Authors: Toft, Mathias Mata, Ignacio F. Ross, Owen A. et al.

Source: Movement Disorders. Feb2007, Vol. 22 Issue 3, p389-392. 4p.

Integrative analysis identifies bHLH transcription factors as contributors to Parkinson's disease risk mechanisms.

Authors: Berge-Seidl, Victoria Pihlstrøm, Lasse Toft, Mathias

Source: Scientific Reports. 2/10/2021, Vol. 11 Issue 1, p1-10. 10p.

LRRK2 mutations and Parkinsonism.

Authors: Toft M Mata IF Kachergus JM et al.

Source: Lancet. 4/2/2005, Vol. 365 Issue 9466, p1229-1230. 2p.

LRRK2 mutations are not common in Alzheimer's disease

Authors: Toft, Mathias Sando, Sigrid Botne Melquist, Stacey et al.

Source: Mechanisms of Ageing & Development. Nov2005, Vol. 126 Issue 11, p1201-1205. 5p.

Epigenome‐wide association study, meta‐analysis, and multiscore profiling of whole blood in Parkinson's disease.

Authors: Lie, Ingeborg Haugesag Tan, Manuela M. X. Andersen, Maren Stolp et al.

Source: Annals of Clinical & Translational Neurology. Apr2025, Vol. 12 Issue 4, p701-713. 13p.

Lysosomal Polygenic Burden Drives Cognitive Decline in Parkinson's Disease with Low Alzheimer Risk.

Authors: Tunold, Jon‐Anders Tan, Manuela M.X. Toft, Mathias et al.

Source: Movement Disorders. Mar2024, Vol. 39 Issue 3, p596-601. 6p.

Parkinson's disease: What remains of the 'missing heritability'?

Authors: Pihlstrøm, Lasse Toft, Mathias

Source: Movement Disorders. Sep2011, Vol. 26 Issue 11, p1971-1973. 3p.