Zobrazeno 1 - 10
of 206
pro vyhledávání: '"Kwang-Hoon Kim"'
Publikováno v:
Advances in Mechanical Engineering, Vol 9 (2017)
During the expansion forming of aluminum tube, the efficiency of heat exchanger diminishes due to the adhesion of groove and expansion ball inside the tube. Despite its importance, a limited number of researches on the adhesion problems in aluminum t
Externí odkaz:
https://doaj.org/article/8c3029e06bae4626a4b64d1644385c3b
Publikováno v:
Buildings, Vol 14, Iss 8, p 2305 (2024)
Safety and crime prevention are significant concerns in both urban and rural areas. Crime Prevention Through Environmental Design (CPTED) guidelines provide an architectural strategy to deter criminal activities by implementing strategic design plans
Externí odkaz:
https://doaj.org/article/83a840ee6df746b3badf7b02bc2c5dc0
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 28, Iss 2, Pp 98-102 (2021)
Hereditary spherocytosis is the most common hereditary red blood cell membrane disorder. It results from a deficiency in certain proteins that are part of the red blood cell membrane cytoskeleton. We report a case of adrenal myelolipoma in a 23-year-
Externí odkaz:
https://doaj.org/article/2251d1732cac4a9a821bf5a538f6d93c
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 28, Iss 1, Pp 39-45 (2021)
Background : : In Korea, in the case of patients with significant bleeding symptoms due to unknown causes, there are very few studies that evaluate bleeding disorders, including von Willebrand disease (VWD). VWD should be considered as an important c
Externí odkaz:
https://doaj.org/article/cf8850254f204feba9cf61def14230f3
Publikováno v:
Computers, Materials & Continua. 70:767-779
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 28, Iss 2, Pp 98-102 (2021)
Hereditary spherocytosis is the most common hereditary red blood cell membrane disorder. It results from a deficiency in certain proteins that are part of the red blood cell membrane cytoskeleton. We report a case of adrenal myelolipoma in a 23-year-
Autor:
Jeong Ho, Ahn, Seung Hwan, Oh, Ji Kyoung, Park, Kwang Hoon, Kim, Jeong Eun, Lee, Woo Yeong, Chung, Keun Soo, Lee, Go Hun, Seo, Bo Lyun, Lee
Publikováno v:
Annals of clinical and laboratory science. 52(3)
Pontocerebellar hypoplasia is a heterogeneous group of rare genetic neurodevelopmental disorders marked by early degeneration of the cerebellum and brainstem. Intellectual developmental disorder with microcephaly and pontine and cerebellar hypoplasia
Publikováno v:
Journal of Institute of Control, Robotics and Systems. 27:443-449
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 28, Iss 1, Pp 39-45 (2021)
Background : : In Korea, in the case of patients with significant bleeding symptoms due to unknown causes, there are very few studies that evaluate bleeding disorders, including von Willebrand disease (VWD). VWD should be considered as an important c
Publikováno v:
IEEE Access. 9:139852-139875
This paper devises an algorithmic process mining framework characterized by the mathematical process model of structured information control nets (SICN) and the concept of mass-driven $\rho $ -function as a decision-making criterion of structural pro