Basma Mohamed^1,*, Linda Mohaisen², Mohammed Amin¹

Intelligent Automation & Soft Computing, Vol.38, No.1, pp. 19-34, 2023, DOI:10.32604/iasc.2023.031947 - 26 January 2024

Abstract In this paper, we consider the NP-hard problem of finding the minimum dominant resolving set of graphs. A vertex set B of a connected graph G resolves G if every vertex of G is uniquely identified by its vector of distances to the vertices in B. A resolving set is dominating if every vertex of G that does not belong to B is a neighbor to some vertices in B. The dominant metric dimension of G is the cardinality number of the minimum dominant resolving set. The dominant metric dimension is computed by a binary version of the Archimedes optimization… More >

Yaojin Sun¹, Nan Jiang^1,*, Min Zhu¹, Hao Hua²

Intelligent Automation & Soft Computing, Vol.38, No.1, pp. 105-105, 2023, DOI:10.32604/iasc.2023.047522 - 26 January 2024

Abstract This article has no abstract. More >

Abdus Saboor^1,4, Arif Hussain², Bless Lord Y. Agbley³, Amin ul Haq^3,*, Jian Ping Li³, Rajesh Kumar^1,*

Intelligent Automation & Soft Computing, Vol.38, No.1, pp. 107-107, 2023, DOI:10.32604/iasc.2023.047463 - 26 January 2024

Abstract This article has no abstract. More >

Tohid Adibi¹, Shams Forruque Ahmed^2,*, Omid Adibi³, Hassan Athari⁴, Irfan Anjum Badruddin⁵, Syed Javed⁵

Intelligent Automation & Soft Computing, Vol.38, No.1, pp. 103-103, 2023, DOI:10.32604/iasc.2023.047521 - 26 January 2024

Abstract This article has no abstract. More >

Fangyu Ye¹, Xiaoshu Xu^2,*, Yunfeng Zhang³, Yan Ye⁴, Jingyu Dai^5,*

Intelligent Automation & Soft Computing, Vol.38, No.1, pp. 101-101, 2023, DOI:10.32604/iasc.2023.045930 - 26 January 2024

Abstract This article has no abstract. More >

Xuming Mo^1,*, Wei Cai^2,*, Jirong Qi¹, Zhuoming Xu³, Ying Wang⁴, Weihui Yan⁴, Shoujun Li⁵, Nianguo Dong⁶, Xinxin Chen⁷, Jinfen Liu³, Qiang Shu⁸, Jimei Chen⁹, Haibo Zhang³, Hao Zhang¹⁰, Quansheng Xing¹¹, Qi An¹², Xiaofeng Li¹³, Xu Wang¹⁴, Yan He¹⁵, Junwu Su¹⁶, Taibing Fan¹⁷, Teng Ming¹⁸, Weibing Tang¹⁹, Li Hong²⁰, Jinghao Zheng³, Ming Ye²¹, Guocheng Sun²², Yiqun Ding²³, Liang Tao²⁴, Yifeng Yang²⁵, Zhongshi Wu²⁵, Hua Cao²⁶, Qiang Wang¹⁶, Keming Yang⁵, Libing Zhang²⁷, Ping Wen²⁸, Yanqin Cui²⁹, Bo Zhai³⁰, Yong Zou¹⁸, Qingya Tang³¹, Rui Chen¹¹, Chun Wu³², Zhiyu Feng³³, Caixia Liu³⁴, Yaping Mi²¹, Rufang Zhang³⁵, Ke Lin¹², Xin Li³⁶, Mingan Pi³⁷, Xiangming Fan⁸, Shanshan Shi³⁸, Peng Huang³⁹, Zhengxia Pan³², Jiafeng Qi⁴⁰, Renwei Chen⁴¹, Shuguang Tao⁴², Yaqin Shu¹, Huifeng Zhang²¹, Lan Jiang¹, Min Da¹, Nishant Patel¹, Liang Hu¹, Cardiac Surgery Group of Pediatric Surgery Society of Chinese Medical Association, Parenteral Enteral Nutrition Society of Chinese Medical Association

Congenital Heart Disease, Vol.18, No.6, pp. 571-593, 2023, DOI:10.32604/chd.2024.048939 - 19 January 2024

Abstract The second edition of the expert consensus on pediatric nutrition was formed based on a global update of pediatric nutrition guidelines or consensus worldwide, the management of congenital heart disease, and the results of multi-center clinical nutrition research for congenital heart disease following the first Chinese consensus edition of 2016. The consensus was also shaped by the results of three discussion sessions and two questionnaires conducted by the 13-member collaboration group. This process was informed by both clinical guidelines and expert consensus. The quality of literature, both in English and Chinese, and the level of More >

Ziguang Song^1,2, Jiangbo Yu¹, Mengmeng Wang³, Weitao Shen⁴, Chengcheng Wang¹, Tianyi Lu¹, Gaojun Shan¹, Guo Dong¹, Yiru Wang¹, Jiyi Zhao^1,*

Congenital Heart Disease, Vol.18, No.6, pp. 693-701, 2023, DOI:10.32604/chd.2024.048081 - 19 January 2024

Abstract CHDTEPDB (URL: ) is a manually integrated database for congenital heart disease (CHD) that stores the expression profiling data of CHD derived from published papers, aiming to provide rich resources for investigating a deeper correlation between human CHD and aberrant transcriptome expression. The development of human diseases involves important regulatory roles of RNAs, and expression profiling data can reflect the underlying etiology of inherited diseases. Hence, collecting and compiling expression profiling data is of critical significance for a comprehensive understanding of the mechanisms and functions that underpin genetic diseases. CHDTEPDB stores the expression profiles of… More >

Aisa Zulibiya^1,2,#, Jing Wen^3,#, Huiqing Yu^3,#, Xiaoming Chen³, Lei Xu³, Xiao Ma^1,2, Baojian Zhang^1,2,*

Congenital Heart Disease, Vol.18, No.6, pp. 611-625, 2023, DOI:10.32604/chd.2023.047689 - 19 January 2024

Abstract Background: Tetralogy of Fallot (TOF) is a very common cyanotic congenital heart disease. Endothelial-to-mesenchymal transition (EndoMT) is recognized as a physiological mechanism involved in embryonic heart development and endothelial formation. However, there is still a gap in the reports related to the mechanism of EndoMT development in TOF. Methods: First, transcriptomic data of single cell nuclei of TOF and Donor were obtained based on the Gene Expression Omnibus (GEO) database, and the data were normalized and clustered by dimensionality reduction using the Seurat package. Subsequently, differentially expressed genes (DEGs) between TOF and Donor were screened… More >

Pier Paolo Bassareo^1,2,3,*, Aurelio Secinaro⁴, Paolo Ciliberti⁵, Massimo Chessa^6,7, Marco Alfonso Perrone^5,8, Kevin Patrick Walsh^1,2,3, Colin Joseph Mcmahon^2,3

Congenital Heart Disease, Vol.18, No.6, pp. 595-610, 2023, DOI:10.32604/chd.2023.046229 - 19 January 2024

Abstract Background: Congenital absence of pericardium (CAP), also known as pericardial agenesis, represents an uncommon cardiac abnormality and mostly incidental finding. It can be subdivided into complete and partial (left or right-sided) forms. Because of its infrequency, just case reports and a few case series have been released so far. This paper represents the largest systematic review in the field. Nine features (age at diagnosis, type, gender, clinical presentation, electrocardiography, imaging (ultrasounds, CT/MRI), concomitant cardiac defects, and outcome) were analysed. Methods: The electronic database PubMed was investigated from its establishment up to July 15^th, 2023. Just case… More >

Dian Kesumarini^1,2, Yunita Widyastuti³, Cindy Elfira Boom¹, Lucia Kris Dinarti^4,*

Congenital Heart Disease, Vol.18, No.6, pp. 671-678, 2023, DOI:10.32604/chd.2023.044746 - 19 January 2024

Abstract Tetralogy of Fallot (TOF) with total anomalous pulmonary vein connections (TAPVC) is a rare type of complex congenital heart disease among all TOF cases. Co-presentation of major aortopulmonary collateral arteries (MAPCAs) compensates for the lack of central pulmonary blood flow and decreases the severity of right-to-left shunting in TOF. We present a case of a 2-year-old child with complex diagnoses of TOF, TAPVC, a large secundum atrial septal defect (ASD), and intraoperatively identified MAPCAs. She underwent surgery to repair the TAPVC, valve-sparing reconstruction of the right ventricular outflow tract, interventricular defect closure, and the creation… More >