Results 181 to 190 of about 2,639,581 (370)

Corrigendum: A Cell Atlas for the Mouse Brain

Frontiers in Neuroinformatics, 2019
Csaba Erö, Marc-Oliver Gewaltig, Daniel Keller, Henry Markram   +3 more
doaj   +1 more source

A differentiation in RNA response in neurons early and late during learning.

, 1965
Holger Hydén, Paul W. Lange
openalex   +1 more source

Nerve Excitability in Asymptomatic Carriers and Amyotrophic Lateral Sclerosis Patients With C9orf72

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We investigated the effects of C9orf72 mutation carriership on peripheral nerve excitability in asymptomatic individuals from families with a history of C9orf72 amyotrophic lateral sclerosis (ALS) and patients. Methods We included 47 asymptomatic individuals from families with a history of C9orf72 ALS, of whom 23 were carriers (C9 ...
Diederik J. L. Stikvoort García, H. Stephan Goedee, Leonard H. van den Berg, Boudewijn T. H. M. Sleutjes   +3 more
wiley   +1 more source

Transduction Mechanisms for Cold Temperature in Mouse Trigeminal and Vagal Ganglion Neurons Innervating Different Peripheral Organs. [PDF]

Acta Physiol (Oxf)
Gers-Barlag K, Del Campo AG, Hernández-Ortego P, Quintero E, Viana F.   +4 more
europepmc   +1 more source

Morphological Studies on the Autonomic Nervous System of Hypertensive Rats : III.Quantitative Estimation of the Cytoplasmic Structure of Neurons in Superior Cervical Sympathetic Ganglia of Spontaneously Hypertensive Rats

, 1969
Masao Matsumoto
openalex   +2 more sources

Physiology of Spinal Neurons, Progress in Brain Research [PDF]

, 1965
R. Werman
openalex   +1 more source

Pyramidal neurons [PDF]

Current Biology, 2011
openaire   +3 more sources

Functional Characterization and Pathogenicity Classification of PRRT2 Splice Variants in PRRT2‐Related Disorders

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu, Yu‐Lan Chen, Wan‐Bing Sun, Hong‐Fu Li, Zhi‐Ying Wu, Dian‐Fu Chen   +5 more
wiley   +1 more source

Familial ALS With p. L127S (L126S) Variant of the Cu/Zn SOD1 Gene: A Report of Two New Cases and Literature Review. [PDF]

Neuropathology
Inoue K, Toyooka K, Fujimura H, Ueda K, Kaido M, Yamamoto Y, Izumi Y.   +6 more
europepmc   +1 more source

Plasma p‐tau181 as a Marker of Conversion to Alzheimer's Disease Dementia and Worsening in Cognitive Functions in Subjective Cognitive Decline and Mild Cognitive Impairment: A Longitudinal Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Plasma p‐tau181 has proven to be a promising diagnostic and prognostic tool in the earliest phases of Alzheimer's disease (AD). We aimed to evaluate the prognostic role of p‐tau181 in predicting conversion to AD dementia and worsening in cognition in mild cognitive impairment (MCI) and subjective cognitive decline (SCD).
Giulia Giacomucci, Assunta Ingannato, Chiara Crucitti, Silvia Bagnoli, Elisa Marcantelli, Sonia Padiglioni, Valentina Moschini, Carmen Morinelli, Laura Falsini, Sandro Sorbi, Valentina Berti, Benedetta Nacmias, Valentina Bessi   +12 more
wiley   +1 more source