Results 181 to 190 of about 182,279 (337)

Neuroimaging of septo-optic dysplasia-plus with midbrain hypoplasia and ophthalmoplegia

, 2020
Colin Y. Wang, Daniel Thomas Ginat
openalex   +1 more source

Nuclear Alpha‐Synuclein: Mechanisms and Implications for Synucleinopathies

Movement Disorders, EarlyView.
Abstract Alpha‐synuclein (aSyn), historically studied for its synaptic functions and central role in Lewy body pathology, is emerging as a protein with significant nuclear activities relevant to Parkinson's disease (PD) and related synucleinopathies. Recent advances reveal that aSyn dynamically localizes to neuronal nuclei in both health and disease ...
Tiago Fleming Outeiro, David J. Koss
wiley   +1 more source

Midbrain

, 2009
Jeremy Jones, Tariq Walizai, Frank Gaillard   +2 more
openaire   +2 more sources

Downbeat nystagmus in association with the dorsal midbrain syndrome: proposed mechanisms, literature review, and case series. [PDF]

Front Neurol
Saab L, Eggenberger ER, Cho C, Friedrich MU, Rucker JC.   +4 more
europepmc   +1 more source

Uncovering the Complexity of Synucleinopathies: An Ongoing Tale Between Proteins and Lipids

Movement Disorders, EarlyView.
Abstract Neurodegenerative diseases are pathological states characterized by progressive alterations in brain homeostasis during aging. Synucleinopathies, including Parkinson's disease and dementia with Lewy bodies, are defined neuropathologically by the accumulation of inclusions known as Lewy bodies and Lewy neurites.
Manuel Flores‐León, Tiago F. Outeiro
wiley   +1 more source

Incidence, Clinician Misdiagnosis Rate, Radiologist Missed Diagnosis Rate, and Lesion Distribution of Isolated Medial Longitudinal Fasciculus Infarction: A Retrospective Study. [PDF]

Int J Gen Med
Wang X, Jing Y, Yang P, Rao F, Wang L, Zhang H, Li M, Liu Q, Zhang Q, Chen J, Xu X, Zhang Q.   +11 more
europepmc   +1 more source

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort

Movement Disorders, EarlyView.
Abstract Background Deep intronic GAA repeat expansions in intron 1 of the FGF14 gene were identified in 2023 as cause of late‐onset cerebellar ataxia. Since then, GAA‐FGF14‐related ataxia (SCA27B) has emerged as one of the most common genetic causes of late‐onset cerebellar ataxia.
Teije H. van Prooije, Maartje Pennings, Roderick P.P.W.M. Maas, Jeroen de Vries, Corien Verschuuren‐Bemelmans, Vincent Odekerken, Sirwan K.L. Darweesh, Mark Huisman, Mayke Oosterloo, Arthur Buijink, Jaron van de Wardt, Els Vanhoutte, Tsz Hang Wong, Lisette Koens, Eva de Boer, Judith van Gaalen, Martijn Beudel, Dareia S. Roos, Jorrit I. Hoff, Thimo Cornelissen, Meyke Schouten, Thatjana Gardeichik, Erica van der Looij, Christine Klein, Joanne Trinh, Erik‐Jan Kamsteeg, Bart van de Warrenburg   +26 more
wiley   +1 more source

Vertebrobasilar dolichoectasia compresses midbrain, worsens Parkinson symptoms, and evokes Holmes tremor: A case report. [PDF]

Medicine (Baltimore)
Li J, Cheng N, Liu T, Rong Q.
europepmc   +1 more source

Shank3 deficiency alters midbrain GABAergic neuron morphology, GABAergic markers and synaptic activity in primary striatal neurons [PDF]

Zuzana Bačová, Bohumila Jurkovičová-Tarabová, Tomáš Havránek, Denisa Mihalj, Veronika Borbélyová, Zdeno Pirník, Boris Mravec, Daniela Ostatníková, Ján Bakoš   +8 more
openalex   +1 more source

Assembly of α4β2 Nicotinic Acetylcholine Receptors Assessed with Functional Fluorescently Labeled Subunits: Effects of Localization, Trafficking, and Nicotine-Induced Upregulation in Clonal Mammalian Cells and in Cultured Midbrain Neurons [PDF]

, 2003
Raad Nashmi, Mary E. Dickinson, Sheri McKinney, Mark Jareb, Cesar Labarca, Scott E. Fraser, Henry A. Lester   +6 more
openalex   +1 more source