Results 41 to 50 of about 410,622 (285)
Energy efficient DBA algorithms for TWDM-PONs [PDF]
, 2015 Energy efficiency is of a vital significance in the design of next generation time and wavelength division multiplexed passive optical networks (TWDM-PONs).
Colle, Didier +4 more
core +2 more sources
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun +95 more
wiley +1 more source
A Rare Cause of Dizziness and Gait Ataxia: CLIPPERS Syndrome
Journal of the Belgian Society of Radiology, 2016 In this paper we report the case of a 52-year-old woman with multiple contrast enhancing lesions associated with a chronic lymphocytic inflammation of the infratentorial structures. We discuss the symptoms, imaging and treatment of this rare disorder, in
Wim Maenhoudt +2 more
doaj +1 more source
Cancer Medicine, 2021 Background The brainstem has the critical role of regulating cardiac and respiratory function and it also provides motor and sensory function to the face via the cranial nerves. Despite the observation of a brainstem lesion in a radiological examination,
In‐Ho Jung +9 more
doaj +1 more source
Optimizing Nutritional Status of Patients Prior to Major Surgical Intervention
Methodist DeBakey Cardiovascular Journal, 2023 In patients undergoing elective cardiovascular and thoracic surgery, malnutrition and the deterioration of nutritional status are associated with negative outcomes.
Raul M. Sanchez Leon +2 more
doaj +1 more source
Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay in Two Half‐Siblings
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) is caused by biallelic pathogenic variants in the SACS gene. We report the clinical, radiologic and neurophysiologic features of a pair of half‐siblings who presented with progressive cerebellar ataxia, peripheral neuropathy and upper motor neuron signs.
Dennis Yeow +6 more
wiley +1 more source
Insights Into the Antigenic Repertoire of Unclassified Synaptic Antibodies
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective We sought to characterize the sixth most common finding in our neuroimmunological laboratory practice (tissue assay‐observed unclassified neural antibodies [UNAs]), combining protein microarray and phage immunoprecipitation sequencing (PhIP‐Seq). Methods Patient specimens (258; 133 serums; 125 CSF) meeting UNA criteria were profiled;
Michael Gilligan +22 more
wiley +1 more source
陆军军医大学学报Objective To investigate whether focal demyelination in the pontine trigeminal tracts (PTTs) can induce trigeminal neuralgia-like behaviors in adult rats.
WEN Jumei, QI Jianguo
doaj +1 more source
Architecture to integrate multiple PONs with long reach DWDM backhaul [PDF]
, 2009 This paper demonstrates the feasibility of an architecture that consolidates a number of deployed Passive Optical Network (PON) infrastructures into a long-reach, high-split ratio system which further increases equipment sharing between users.
Mitchell, J.E., Shea, D.P.
core +1 more source
An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco +7 more
wiley +1 more source