Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Chi Ren Tsai"'
Publikováno v:
Archives of Disease in Childhood; Sep2024, Vol. 109 Issue 9, p730-735, 12p
Autor:
Hui-Hsien Pan, Chi-Ren Tsai, Pei-Ju Ting, Fang-Liang Huang, Li-Chung Wang, Chin-Fu Lin, Jiunn-Liang Ko, Ko-Huang Lue, Po-Yen Chen
Publikováno v:
Pediatrics and Neonatology, Vol 61, Iss 2, Pp 168-173 (2020)
Background: Enterovirus-D68 (EV-D68) has been endemic in Taiwan for some years with a small number of positive cases. Detailed information about respiratory presentation is lacking. This study characterized the clinical course in children admitted to
Externí odkaz:
https://doaj.org/article/1f636b69901f4d4cbe979bb89dacf05a
Publikováno v:
Children, Vol 10, Iss 2, p 182 (2023)
Background: Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is the most common autoimmune encephalitis in children. There is a high probability of recovery if treated promptly. We aimed to analyze the clinical features and long-term outcomes o
Externí odkaz:
https://doaj.org/article/639c8f4ac5904317aaa81bda98900319
Publikováno v:
Brain Sciences, Vol 12, Iss 9, p 1262 (2022)
Background: This work aims to describe the clinico-radiological phenotype of UBTF c.628G>A (p.Glu210Lys) pathogenic variant-related neurodegeneration in childhood. Methods: We describe the progress of clinical and neuroimaging features in a male indi
Externí odkaz:
https://doaj.org/article/9558c62fe94840099d821b0bf89f93ea
Publikováno v:
Children, Vol 8, Iss 8, p 617 (2021)
Frasier syndrome is a rare disease that affects the kidneys and genitalia. Patients who have Frasier syndrome develop nephrotic syndrome (NS) featuring focal segmental glomerulosclerosis (FSGS) that is resistant to steroid treatment in early childhoo
Externí odkaz:
https://doaj.org/article/1fb417f6c9784e059f535f6e07fd1627
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-5 (2017)
Abstract Background Isolated sulfite oxidase deficiency (ISOD) is a very rare autosomal recessive inherited neurometabolic disease. The most striking postnatal neuroimaging finding is multicystic encephalomalacia, which occurs rapidly within days to
Externí odkaz:
https://doaj.org/article/5c757f2589fd45ee976d5863167f8eb8
Publikováno v:
Human Genetics.
Publikováno v:
Neuropediatrics. 53:200-203
Background To describe the genotype-phenotype dissociation in two Taiwanese patients with molybdenum cofactor deficiency (MoCoD) caused by MOCS2 gene mutations. Patient Description Patient 1 exhibited early-onset neurological symptoms soon after birt
Publikováno v:
Pediatrics and Neonatology, Vol 55, Iss 6, Pp 449-454 (2014)
The primary aim of the study was to investigate the changes in composition of breast milk from mothers with preterm infants (gestation age
Externí odkaz:
https://doaj.org/article/2a0d836c746845f386d5ee5716697218
Publikováno v:
Pediatrics and Neonatology, Vol 54, Iss 6, Pp 360-366 (2013)
The bioactive proteins in human milk may be influenced by prolonged storage process, pasteurization, and heat treatment. This study was conducted to evaluate the effects of these procedures. Materials and methods: Three forms of human milk – freshl
Externí odkaz:
https://doaj.org/article/5cdcfb42b2fe4ab9b7f55cc4f5b96343