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HARQ Optimization for PDCP Duplication-Based 5G URLLC Dual Connectivity

Computers, Materials & Continua 2022年第7期72卷 727-738页

作者： Changsung Lee junsung kim Jaewook Jung Jungsuk Baik Jong-Moon Chung Samsung Research Seoul06765Korea Samsung Electronics Suwon16677Korea School of Electrical and Electronic Engineering Yonsei UniversitySeoul03722Korea

Packet duplication(PD)with dual connectivity(DC)was newly introduced in the 5G New Radio(NR)specifications to meet the stringent ultra reliable low latency communication(URLLC)*** technology uses duplicated packets in the packet data convergence protocol(PDCP)layer that are transmitted via two different access nodes(ANs)to the user equipment(UE)in order to enhance the reliability ***,PD can result in unnecessary retransmissions in the lower layers since the hybrid automatic retransmission request(HARQ)operation is unaware of the transmission success achieved through the alternate DC link to the *** overcome this issue,in this paper,a novel duplication-aware retransmission optimization(DRO)scheme is proposed to reduce the resource usage induced by unnecessary HARQ *** proposed DRO scheme can minimize the average channel use while satisfying the URLLC *** proposed DRO scheme derives the optimal HARQ retransmission attempts for different ANs by solving a nonlinear integer programming(NLIP)*** performance of the proposed DRO scheme was evaluated using MATLAB simulation and is compared to the existing 5G HARQ support *** simulations results show that the proposed DRO scheme can provide a 14.71%and 15.11%reduced average channel use gain compared to the selective data duplication upon failure(SDUF)scheme and latency-aware dynamic multi-connectivity algorithm(LADMA)scheme,respectively,which are the existing 5G PD schemes that use HARQ.

关键词： 5G networks URLLC dual connectivity retransmission packet duplication

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High Prevalence of Genetic Alterations in Infantile-Onset Cardiomyopathy

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Congenital Heart Disease 2021年第4期16卷 397-410页

作者： junsung Park Go Hun Seo Yena Lee Yunha Choi Minji Kang Hyo-Sang Do Young-Hwue kim Jeong Jin Yu Ellen Ai-Rhan kim Euiseok Jung Byong Sop Lee Jae Suk Baek Beom Hee Lee Department of Pediatrics Asan Medical CenterUniversity of Ulsan College of MedicineSeoulKorea billion Inc.SeoulKorea Genome Research Center for Birth Defects and Genetic Diseases Asan Institute for Life SciencesAsan Medical CenterSeoulKorea Division of Cardiology Department of PediatricsAsan Medical CenterUniversity of Ulsan College of MedicineSeoulKorea Division of Neonatology Department of PediatricsAsan Medical CenterUniversity of Ulsan College of MedicineSeoulKorea Medical Genetics Center Asan Medical Center Children’s HospitalUniversity of Ulsan College of MedicineSeoulKorea

Background and Method:The genetic cause of infantile-onset cardiomyopathy is rarely ***,we conducted whole exome sequencing(WES)and mitochondrial DNA(mtDNA)sequencing in eight patients with infantile-onset cardiomyopathy to identify genetic ***:Among these patients,two(25%)had dilated cardiomyopathy(DCMP),two(25%)had left ventricular non-compaction(LVNC),and four(50%)had hypertrophic cardiomyopathy(HCMP).Except four patients identified prenatally,the remaining patients presented at a median age of 85.5 *** identified genetic variants in a total of seven(87.5%)patients and mtDNA sequencing in the other ***1 and MYH7 variants were identified in the two patients with DCMP;MYH11 and MYLK2 variants in the two patients with LVNC;HRAS,BRAF,and MYH7 variants in three patients with HCMP;and MT-ND1 variant in one patient with HCMP having high blood lactic acid *** the eight variants,four were classified as pathogenic or likely-pathogenic according to the American College of Medical Genetics(ACMG)guidelines,and the remaining were identified as variants of unknown significance(VUSs).Three pathogenic mutations were de novo,whereas four(likely-pathogenic or VUSs)were inherited from a respective parent,excluding one variant where parental testing was unavailable,questioning whether these inherited variants are *** patients died before 3 months of ***:Genomic studies,such as WES with additional mtDNA sequencing,can identify a genetic variant in high proportions of patients with infantile-onset *** clinical implication of the parentally inherited variant needs to be assessed in a larger patient and family cohort with a longitudinal follow-up.

关键词： Cardiomyopathy whole exome sequencing infantile-onset

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Prognostic value of pre-treatment F-18-FDG PET-CT in patients with hepatocellular carcinoma undergoing radioembolization

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World Journal of Gastroenterology 2016年第47期22卷 10406-10414页

作者： Yazan Abuodeh Arash O Naghavi Kamran A Ahmed Puja S Venkat Youngchul kim Bela Kis junsung Choi Benjamin Biebel Jennifer Sweeney Daniel A Anaya Richard kim Mokenge Malafa Jessica M Frakes Sarah E Hoffe Ghassan El-Haddad Department of Radiation Oncology H Lee Moffitt Cancer Center and Research Institute Department of Interventional Radiology H Lee Moffitt Cancer Center and Research Institute Department of Gastrointestinal Oncology H Lee Moffitt Cancer Center and Research Institute

AIM To evaluate the value of pre-treatment 18F-FDG PET/CT in patients with HCC following liver *** We identified 34 patients with HCC who underwent an FDG PET/CT scan prior to hepatic radioembolization at our institution between 2009 and 2013. Patients wereseen in clinic one month after radioembolization and then at 2-3 mo intervals. We assessed the influence of FDG tumor uptake on outcomes including local liver control(LLC), distant liver control(DLC), time to distant metastases(DM), progression free survival(PFS) and overall survival(OS).RESULTS The majority of patients were males(n = 25, 74%), and had Child Pugh Class A(n = 31, 91%), with a median age of 68 years(46-84 years). FDG-avid disease was found in 19(56%) patients with SUVmax ranging from 3 to 20. Female patients were more likely to have an FDG-avid HCC(P = 0.02). Median follow up of patients following radioembolization was 12 months(1.2-62.8 mo). FDG-avid disease was associated with a decreased 1 year LLC, DLC, DM and PFS(P < 0.05). Using multivariate analysis, FDG avidity predicted for LLC, DLC, and PFS(all P < 0.05).CONCLUSION In this retrospective study, pre-treatment HCC FDGavidity was found to be associated with worse LLC, DLC, and PFS following radioembolization. Larger studies are needed to validate our initial findings to assess the role of F-18-FDG PET/CT scans as biomarker for patients with HCC following radioembolization.

关键词： F-18 fluorodeoxyglucose 宠物 Hepatocellular 癌 Radioembolization 预后 Biomarker

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