Results 121 to 130 of about 4,800 (298)
Riffles, ruffles, and the turning algebra
, 2008 Version dated 13 November 1995; GNU ...
Doyle, Peter G., Rockmore, Dan
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li +11 more
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Judy Riffle named American Chemical Society Fellow
, 2010 Judy S. Riffle, professor of chemistry and director of Virginia Tech's interdisciplinary Macromolecular Science and Engineering Ph.D. education program, has been named a Fellow of the American Chemical Society.
Doss, Catherine
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
Rathburn Run riffle 1, 08-2011
, 2011 A standing wave at a riffle in Rathburn Run looking southwest. At center is a glacial erratic. Field Camera: Nikon D90 digital SLR.
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Water Resources ResearchRestoring streams by feeding sediment from a single location is cost‐effective, allowing natural sediment distribution. Alternatively, placing sediment in predetermined patterns requires more planning but may provide controlled improvements to flow and ...
Nisreen G. Al‐Ghorani +6 more
doaj +1 more source
Universality of Cutoff for Riffle Shuffling
61 ...
Sellke, Mark, Shi, Jialu, Wang, Jiamin
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A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
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Ictelmis, a new riffle beetle genus from Ecuador (Coleoptera: Elmidae)
, 2019 Čiampor, Fedor, Linský, Marek, Čiamporová-Zaťovičová, Zuzana (2019): Ictelmis, a new riffle beetle genus from Ecuador (Coleoptera: Elmidae). Zootaxa 4695 (5): 483-491, DOI: https://doi.org/10.11646/zootaxa.4695.5.
Čiamporová-Zaťovičová, Zuzana +2 more
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White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian +8 more
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