Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Naye Choi"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 8, Pp n/a-n/a (2024)
ABSTRACT Introduction Holocarboxylase synthetase deficiency (HLCS deficiency, OMIM #253270) is an exceedingly rare metabolic disorder resulting in multiple carboxylase deficiencies owing to impaired biotin cycle. Clinical manifestations include sever
Externí odkaz:
https://doaj.org/article/4959441a6d4c46a5a75fbc5c95d12ccf
Publikováno v:
Childhood Kidney Diseases, Vol 27, Iss 2, Pp 105-110 (2023)
Purpose To analyze electrocardiograms (ECGs) of patients with a salt-losing tubulopathy (SLT) and to determine the frequency and risk factors for long QT and arrhythmia. Methods A total of 203 patients aged
Externí odkaz:
https://doaj.org/article/8fd4e54caef74ce7b75bca728a309683
Publikováno v:
Kidney Research and Clinical Practice, Vol 42, Iss 6, Pp 731-741 (2023)
Background Donor–recipient size mismatching is commonly occurs in pediatric kidney transplantation (KT). However, its effect on graft survival remains unknown. This study aimed to determine the effect of donor–recipient size mismatch on the long-
Externí odkaz:
https://doaj.org/article/facb16afe42949b0b6596985611c1c82
Autor:
Naye Choi, Seung-Ah Choe, Yo Han Ahn, Young June Choe, Ju-Young Shin, Nam-Kyong Choi, Seong Heon Kim, Hee Gyung Kang
Publikováno v:
Childhood Kidney Diseases, Vol 27, Iss 1, Pp 34-39 (2023)
Purpose This article was to collect data on the safety of coronavirus disease 2019 (COVID-19) vaccines in children with underlying medical conditions. Methods We constructed a prospective cohort of children and adolescents aged 5 to 19 years who had
Externí odkaz:
https://doaj.org/article/3fb8784971c548b893d9ef7b08c0a1b7
Publikováno v:
Childhood Kidney Diseases, Vol 27, Iss 1, Pp 26-33 (2023)
Purpose Hematuria and proteinuria have various causes and consequential outcomes in children. Immunosuppressants are needed in some children with biopsy-proven glomerulonephropathy but have many adverse effects. Since the clinical practice patterns o
Externí odkaz:
https://doaj.org/article/556562f6d4c845eabd521a6eaff860b5
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101252- (2024)
Externí odkaz:
https://doaj.org/article/0899c3fd3e6d4bfd8abc3cd69922b892
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101251- (2024)
Externí odkaz:
https://doaj.org/article/f2ccd4b5afc84ba8bd86dbb76321b707
Autor:
Naye Choi, Seong Heon Kim, Eun Hui Bae, Eun Mi Yang, Keum Hwa Lee, Sang-Ho Lee, Joo Hoon Lee, Yo Han Ahn, Hae Il Cheong, Hee Gyung Kang, Hye Sun Hyun, Ji Hyun Kim
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/b52d8c8ecaf84e7ca9152ad459795751
Autor:
Naye Choi, Seong Heon Kim, Eun Hui Bae, Eun Mi Yang, Keum Hwa Lee, Sang-Ho Lee, Joo Hoon Lee, Yo Han Ahn, Hae Il Cheong, Hee Gyung Kang, Hye Sun Hyun, Ji Hyun Kim
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionBartter syndrome (BS) is a rare salt-wasting tubulopathy caused by mutations in genes encoding sodium, potassium, or chloride transporters of the thick ascending limb of the loop of Henle and/or the distal convoluted tubule of the kidney.
Externí odkaz:
https://doaj.org/article/7390a638d0da4dad894483491fd3f8d2
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
Single gene pathogenic mutations have been implicated in up to 30% of pediatric steroid-resistant nephrotic syndrome (SRNS) cases, mostly in infantile patients. Among them is LAMA5, which has been recently discovered and encodes the laminin α5 chain
Externí odkaz:
https://doaj.org/article/6a19d6501ef643b89998c95a8ec4a366