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A mostrar 1 - 20 resultados de 176 para a pesquisa '(( j w compere a new ) OR ((( 3 details from u net ) OR ( 3 a company a ngoc ))))', tempo de pesquisa: 0.78seg Refinar resultados
Fine-Grain Segmentation of the Intervertebral Discs from MR Spine Images Using Deep Convolutional Neural Networks: BSU-Net
Fine-Grain Segmentation of the Intervertebral Discs from MR Spine Images Using Deep Convolutional Neural Networks: BSU-Net

Planktonic Cyanobacteria forming blooms in reservoirs of northeastern Brazil
AB156. Clinical and laboratory characteristics of Prader-Willi syndrome

AB112. Spectrum of mucopolysaccharidoses in Vietnam
Multi-Level and Multi-Scale Feature Aggregation Network for Semantic Segmentation in Vehicle-Mounted Scenes

The sensitivity of cash flows to cash holdings: case studies at Vietnamese enterprises
State Differences in the Reporting of Diabetes-Related Incorrect Cause-of-Death Causal Sequences on Death Certificates

DEEP LEARNING BASED BUILDING FOOTPRINT EXTRACTION FROM VERY HIGH RESOLUTION TRUE ORTHOPHOTOS AND NDSM
AB101. Neonatal form of Isovaleric acidemia in Vietnamese patients: clinical history and outcomes

AB074. Registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam during 15 years
AB124. Mucolipidosis type II: clinical features and laboratories

AB020. Chromosome rearrangement in patients with 46,XY disorders of sex development
AB099. Beta ketothiolase deficiency: phenotype and genotype in Vietnam population

AB069. Effect of osteogenesis imperfecta on children and their families
Defective Glycogenesis Contributes Toward the Inability to Suppress Hepatic Glucose Production in Response to Hyperglycemia and Hyperinsulinemia in Zucker Diabetic Fatty Rats

AB102. Vietnamese patient with Tyrosinemia type 1: a case report
Molecular bases for the constitutive photomorphogenic phenotypes in Arabidopsis

AB032. Mutation spectrum in the dystrophin gene disclosed by multiplex ligation-dependent probe amplification in 181 Vietnamese Duchenne/Becker muscular dystrophy patients
AB078. Novel mutation of ABCC8 and KCNJ11 of children with congenital hyperinsulinism

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