Results 91 to 100 of about 5,463 (156)

Research productivity of the Department of Neurosciences of the University of the Philippines Manila: a bibliometric analysis

open access: yesCogent Education
Research output is widely recognized as a key indicator of productivity and a measure of the status of a nation’s research activity. This bibliometric analysis examined the research productivity of the Department of Neurosciences at the University of the
Mykha Marie B. Tabuzo   +3 more
doaj   +1 more source

Retrotransposon: an insight into neurological disorders from perspectives of neurodevelopment and aging

open access: yesTranslational Neurodegeneration
Neurological disorders present considerable challenges in diagnosis and treatment due to their complex and diverse etiology. Retrotransposons are a type of mobile genetic element that are increasingly revealed to play a role in these diseases.
Wenchuan Zhang   +6 more
doaj   +1 more source

Insights into molecular mechanisms of disease in Neurodegeneration with Brain Iron Accumulation; unifying theories.

open access: yes, 2016
Neurodegeneration with brain iron accumulation (NBIA) is a group of disorders characterised by dystonia, parkinsonism and spasticity. Iron accumulates in the basal ganglia and may be accompanied by Lewy bodies, axonal swellings and hyperphosphorylated ...
Arber, C   +7 more
core   +1 more source

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

open access: yes, 2017
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
Vincent Cheah
core   +1 more source

Disease onset in X-linked dystonia-parkinsonism correlates with expansion of a hexameric repeat within an SVA retrotransposon in TAF1

open access: yes, 2017
Significance The genetic basis of X-Linked dystonia-parkinsonism (XDP) has been difficult to unravel, in part because all patients inherit the same haplotype of seven sequence variants, none of which has ever been identified in ...
Rachita Yadav   +20 more
core   +1 more source

Beyond the Homunculus—SCAN‐AMN as a Shared Action‐Oriented Neural Substrate across Movement Disorders

open access: yes
Movement Disorders, Volume 41, Issue 6, Page 1349-1354, June 2026.
Arjun Balachandar   +4 more
wiley   +1 more source

Electrophysiological biomarkers in genetic movement disorders

open access: yes, 2008
BACKGROUND. Neurodegenerative diseases are diseases of the nervous system with progressive course leading to death. Treatment remains symptomatic. Development of neuroprotective agents has been hampered for various reasons. This includes the inability of
Schneider, K.S.A.I.M
core  

Establishing a natural history of X-linked dystonia parkinsonism. [PDF]

open access: yesBrain Commun, 2023
Acuna P   +20 more
europepmc   +1 more source

Oculomotor abnormalities indicate early executive dysfunction in prodromal X-linked dystonia-parkinsonism (XDP). [PDF]

open access: yesJ Neurol, 2023
Mertin R   +12 more
europepmc   +1 more source

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