Results 131 to 140 of about 1,028,974 (354)
Journal of Applied Clinical Medical Physics, EarlyView.Abstract Purpose This study aims to develop a CycleGAN based denoising model to enhance the quality of low‐dose PET (LDPET) images, making them as close as possible to standard‐dose PET (SDPET) images. Methods Using a Philips Vereos PET/CT system, whole‐body PET images of fluorine‐18 fluorodeoxyglucose (18F‐FDG) were acquired from 37 patients to ...
Yang Liu, ZhiWu Sun, HaoJia Liu
wiley +1 more source
UDP‐glucose dehydrogenase variants cause dystroglycanopathy
Annals of Clinical and Translational Neurology, EarlyView.Abstract UDP‐glucose dehydrogenase (UGDH) variants have been associated with hypotonia, developmental delay, and epilepsy. We report the first pathologic evidence of dystroglycanopathy in siblings with UGDH variants. Both presented around 6 months with developmental delay and elevated creatinine kinase.
Anna M. Reelfs +8 more
wiley +1 more source
Univalent functions related to q–analogue of generalized M–series with respect to k–symmetric points [PDF]
Surveys in Mathematics and its Applications, 2019 n this paper, we introduce subclasses of analytic functions by using q-analogue of generalized M-series and k-symmetric points. Some special coefficient inequalities are also discussed.
Sh. Najafzadeh
doaj
Univalence for convolutions [PDF]
International Journal of Mathematics and Mathematical Sciences, 1996 The radius of univalence is found for the convolution f∗g of functions f ∈ S (normalized univalent functions) and g ∈ C (close‐to‐convex functions). A lower bound for the radius of univalence is also determined when f and g range over all of S. Finally, a characterization of C provides an inclusion relationship.
openaire +3 more sources
Progressive Myoclonus Epilepsy: Distinctive MRI Changes in Cerebellar and Motor Networks
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Progressive myoclonus epilepsy (PME) is a rare generalized epilepsy syndrome with a well‐characterized genetic basis. The brain networks that are affected to give rise to the distinctive symptoms of PME are less well understood. Methods Eleven individuals with PME with a confirmed genetic diagnosis and 22 controls were studied.
Jillian M. Cameron +3 more
wiley +1 more source
Comb Convolution for Efficient Convolutional Architecture
, 2019 15 ...
Li, Dandan +3 more
openaire +2 more sources
Early Language Impairment as an Integral Part of the Cognitive Phenotype in Huntington's Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Huntington's disease (HD) speech/language disorders have typically been attributed to motor and executive impairment due to striatal dysfunction. In‐depth study of linguistic skills and the role of extrastriatal structures in HD is scarce.
Arnau Puig‐Davi +13 more
wiley +1 more source
Generalizing the Convolution Operator in Convolutional Neural Networks [PDF]
Neural Processing Letters, 2019 Neural Process Lett (2019)
openaire +3 more sources
Cerebello‐Prefrontal Connectivity Underlying Cognitive Dysfunction in Spinocerebellar Ataxia Type 2
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Spinocerebellar ataxia type 2 (SCA2) is a hereditary cerebellar degenerative disorder, with motor and cognitive symptoms. The constellation of cognitive symptoms due to cerebellar degeneration is named cerebellar cognitive affective syndrome (CCAS), which has increasingly been recognized to profoundly impact patients' quality of life;
Ami Kumar +7 more
wiley +1 more source