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Case report

Lubag Syndrome (X-linked Dystonia Parkinsonism) Case Study of Mr G. Infante

Sex-linked dystonia parkinsonism (XDP) also known as Lubag Syndrome is a rare sex-linked genetic progressive movement disorder affecting almost exclusively males from the province of Capiz in the Philippines and their descendants. At the Mater Centre for Neurosciences we have recently treated two patients with XDP utilising Deep Brain Stimulation (DBS) implants. Mr G. Infante was the second patient to be treated, the first being his uncle. Mr G. Infante’s case was brought to the attention of

Vincent Cheah

Australasian Journal of Neuroscience , ISSUE 1, 7–10

Research paper

Afferent projections of the subthalamic nucleus in the rat: emphasis on bilateral and interhemispheric connections

The subthalamic nucleus (STN) is important for normal movement as well as in movement disorders. The STN is a target nuclei in patients with advanced Parkinson’s disease (PD). Deep brain stimulation (DBS) is a standard surgical treatment for PD. Although DBS results in a significant reduction in motor disability, several negative side effects have been reported. Thus, to understand the side effects of DBS the connection of the STN should be well known. Therefore, the present study aims to re

Safiye Çavdar, Merve Özgür, Yusuf Özgür Çakmak, Yasemin Kuvvet, Sıla Kezban Kunt, Gökay Sağlam

Acta Neurobiologiae Experimentalis , ISSUE 3, 251–263

Review Paper

Neurostimulation, neuromodulation, and the treatment of epilepsies

Introduction. Neurostimulation and neuromodulation are techniques that may be able to affect the course of epilepsy. In the last 20 years, since the approval of VNS, we have observed a surge of studies assessing the potential of other devices and techniques for the treatment of pharmacoresistant epilepsies including deep brain stimulation (DBS), responsive neurostimulation (RNS), trigeminal nerve stimulation (TNS), transcranial direct current stimulation (tDCS), and repetitive transcranial

Lauren B. Bolden, Sandipan Pati, Jerzy P. Szaflarski

Journal of Epileptology , ISSUE 1, 45–59

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