Results 171 to 180 of about 86,125 (297)

Cerebellar contributions to dystonia: unraveling the role of Purkinje cells and cerebellar nuclei. [PDF]

Dystonia
Jackson NN, Stagray JA, Snell HD.
europepmc   +1 more source

Cerebellar nuclei evolved by repeatedly duplicating a conserved cell-type set. [PDF]

Science, 2020
Kebschull JM, Richman EB, Ringach N, Friedmann D, Albarran E, Kolluru SS, Jones RC, Allen WE, Wang Y, Cho SW, Zhou H, Ding JB, Chang HY, Deisseroth K, Quake SR, Luo L.   +15 more
europepmc   +1 more source

The Spectrum of Abnormal Tongue Movements: Review of Phenomenology, Etiology, and Differential Diagnosis

Movement Disorders Clinical Practice, EarlyView.
ABSTRACT Background Classifying abnormal tongue movements is challenging due to their varied presentations and limited visibility compared to other body parts. Accurate identification of the phenomenology guides physical examination and can point to specific diagnoses.
Nathaniel Bendahan, Seyed‐Mohammad Fereshtehnejad, Christos Ganos, Emily Swinkin, Anthony E. Lang   +4 more
wiley   +1 more source

Projections from Regions of the Cerebellar Nuclei Receiving Jaw Muscle Proprioceptive Signals to Trigeminal Motoneurons and Their Premotoneurons in the Rat Pons and Medulla. [PDF]

Cerebellum
Sato F, Tsutsumi Y, Oka A, Furuta T, Sohn J, Oi Y, Amano M, Morita A, Uchino K, Kato T, Bae YC, Tachibana Y, Sessle BJ, Yoshida A.   +13 more
europepmc   +1 more source

Dysfunction of parvalbumin neurons in the cerebellar nuclei produces an action tremor. [PDF]

J Clin Invest, 2020
Zhou M, Melin MD, Xu W, Südhof TC.
europepmc   +1 more source

Aberrant outputs of cerebellar nuclei and targeted rescue of social deficits in an autism mouse model. [PDF]

Protein Cell
Cai XY, Wang XT, Guo JW, Xu FX, Ma KY, Wang ZX, Zhao Y, Xie W, Schonewille M, De Zeeuw C, Chen W, Shen Y.   +11 more
europepmc   +1 more source

TULP4, a novel E3 ligase gene, participates in neuronal migration as a candidate in schizophrenia

CNS Neuroscience &Therapeutics, EarlyView., 2023
Mutations identified from four SCZ pedigrees resulted in decreased TULP4 expression. Tulp4 knockdown caused delayed neuron migration in embryonic mice, and impaired cognition and prepulse inhibition in adult mice. These phenotypes may be related to TULP4 through its involvement in the formation of a novel E3 ubiquitin ligases.
Yan Bi, Decheng Ren, Fan Yuan, Zhou Zhang, Daizhan Zhou, Xin Yi, Lei Ji, Keyi Li, Fengping Yang, Xi Wu, Xingwang Li, Yifeng Xu, Yun Liu, Peng Wang, Changqun Cai, Chuanxin Liu, Qian Ma, Lin He, Yi Shi, Guang He   +19 more
wiley   +1 more source

Adolescent Cerebellar Nuclei Manipulation Alters Reversal Learning and Perineuronal Net Intensity Independently in Male and Female Mice. [PDF]

J Neurosci
Lyle TT, Verpeut JL.
europepmc   +1 more source

Morphological Features of the Cerebellar Nuclei

Galician Medical Journal, 2015
Modern neurological clinic, as well as neurosurgery and neuromorphology, constantly require further research of the morphological structure of the cerebellar nuclei. The study of clinical anatomy of the cerebellar nuclei, as well as their functional characteristics is necessary for clinicians to elaborate rational surgical access to these structures ...
openaire   +4 more sources

Convergence Deficits in Myoclonus‐Dystonia Point to Cerebellar Impairment

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Myoclonus‐dystonia (M‐D) is a monogenic movement disorder, with proposed cerebellar dysfunction. Vergence eye movement deficits, characteristics of degenerative cerebellar disease, have not been studied in M‐D. Cerebellar transcranial alternating current stimulation (tACS) is considered a potential therapeutic approach.
Skadi Gerkensmeier, Christina Bolte, Jan‐Ole Radecke, Feline Hamami, Andreas Sprenger, Christoph Helmchen, Robert Chen, Marcus Callister, Talyta Cortez Grippe, Christine Klein, Norbert Brüggemann, Tobias Bäumer, Alexander Münchau, Anne Weissbach   +13 more
wiley   +1 more source