Results 31 to 40 of about 1,080,409 (319)

Defect Tolerance in Hybrid nano/CMOS Architecture using Tagging Mechanism [PDF]

open access: yes, 2009
In this paper we propose two efficient repair techniques for hybrid nano/CMOS architecture to provide high level of defect tolerance at a modest cost.We have applied the proposed techniques to a lookup table(LUT) based Boolean logic approach.
Srivastava, Saket   +5 more
core   +1 more source

Diagnostic Value and Effectiveness of an Artificial Neural Network in Biliary Atresia

open access: yesFrontiers in Pediatrics, 2020
Objectives: Biliary atresia (BA) is a devastating pediatric liver disease. Early diagnosis is important for timely intervention and better prognosis.
Jia Liu   +7 more
doaj   +1 more source

A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family

open access: yesMolecular Cytogenetics, 2020
Background Copy number variants (CNVs) associated with developmental delay and intellectual disability (DD/ID) continue to be identified in patients. This article reports identification of a chromosome 1q22 microdeletion as the genetic cause in a Chinese
Hui Xi   +7 more
doaj   +1 more source

A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8

open access: yesMolecular Genetics & Genomic Medicine, 2021
Background Nemaline myopathy 8 is a severe autosomal recessive muscle disorder characterized by fetal akinesia or hypokinesia, contractures, fractures, respiratory failure and swallowing difficulties apparent at birth.
Sheng Yi   +13 more
doaj   +1 more source

Highly-Sensitive and Frequency-Selective Imaging of Defects via Local Defect Resonance [PDF]

open access: yes, 2014
In this paper, a consistent way to enhance acoustic, optical and thermal defect responses is suggested by using selective ultrasonic activation of defects based on the concept of local defect resonance (LDR).
Solodov Igor   +2 more
core   +1 more source

A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5

open access: yesBMC Medical Genetics, 2020
Background Neuronal ceroid lipofuscinosis type 5 (CLN5) is a rare form of neuronal ceroid lipofuscinoses (NCLs) which are a group of inherited neurodegenerative diseases characterized by progressive intellectual and motor deterioration, visual failure ...
Wei Li   +10 more
doaj   +1 more source

Development and Assessment of Screening Nomogram for Biliary Atresia Based on Hepatobiliary Ultrasonographic Features

open access: yesFrontiers in Pediatrics, 2021
Objectives: Biliary atresia (BA) is a rare neonatal liver disease of which the early diagnosis remains a challenge for clinicians. Our center has established a nomogram diagnostic model based on clinical characteristics and liver function characteristics.
Shu Yang Dai   +6 more
doaj   +1 more source

Data quality: Some comments on the NASA software defect datasets [PDF]

open access: yes, 2013
Background-Self-evidently empirical analyses rely upon the quality of their data. Likewise, replications rely upon accurate reporting and using the same rather than similar versions of datasets.
Mair, C   +7 more
core   +1 more source

Defects and defect engineering in Soft Matter

open access: yesSoft Matter, 2020
Defect engineering is a success story in crystalline hard matter; this review summarizes its parallels in amorphous soft matter.
Amir Jangizehi   +4 more
openaire   +4 more sources

Observations of changes in acoustic emission waveform for varying seeded defect sizes in a rolling element bearing [PDF]

open access: yes, 2009
The investigation reported in this paper was centered on the application of the acoustic emissions (AE) technology for characterising the defect sizes on a radially loaded bearing.
Mba, David   +2 more
core   +1 more source

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