Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kyo Ryung Kim"'
Autor:
Jung Hyun Chae, Jung Hun Lee, Kyo Ryung Kim, Suk Ho Byeon, Young Mock Lee, Hoon Chul Kang, Joon Soo Lee, Heung Dong Kim
Publikováno v:
Korean Journal of Pediatrics, Vol 53, Iss 12, Pp 994-999 (2010)
PurposeMitochondrial dysfunction can present with various symptoms depending on the organ it has affected. This research tried to analyze the ophthalmologic symptoms and ophthalmologic examination (OE) results in patients with mitochondrial disease (
Externí odkaz:
https://doaj.org/article/1f31bb9c5113427daabd0abcab36a367
Publikováno v:
Korean Journal of Pediatrics, Vol 53, Iss 2, Pp 163-166 (2010)
Purpose : Leigh syndrome is a typical type of mitochondrial disease. This study was conducted to analyze the types of ophthalmologic symptoms and results of funduscopy conducted in the ophthalmologic examination of patients with Leigh syndrome. Metho
Externí odkaz:
https://doaj.org/article/8fdb88cd17aa47979c363c8b43f43dc3
Autor:
Jun Seok Lee, Kyo Ryung Kim, Jeong Tae Kim, Min Jung Choi, Young Mock Lee, Heung Dong Kim, Joon Soo Lee, Dong Seok Kim, Tae Seong Kim
Publikováno v:
Korean Journal of Pediatrics, Vol 53, Iss 1, Pp 106-110 (2010)
Hippocampal sclerosis (HS) is one of the most common features of intractable temporal lobe epilepsy. Generally it can be identified through brain magnetic resonance imaging (MRI) with high degree of sensitivity and specificity. Typical brain MRI find
Externí odkaz:
https://doaj.org/article/39cceb62a8f048eb9e6b6ff4c9def71b
Autor:
Hoon Chul Kang, Young Mock Lee, Joon Soo Lee, Heung Dong Kim, Suk Ho Byeon, Jung Hun Lee, Jung Hyun Chae, Kyo Ryung Kim
Publikováno v:
Korean Journal of Pediatrics
Korean Journal of Pediatrics, Vol 53, Iss 12, Pp 994-999 (2010)
Korean Journal of Pediatrics, Vol 53, Iss 12, Pp 994-999 (2010)
Purpose Mitochondrial dysfunction can present with various symptoms depending on the organ it has affected. This research tried to analyze the ophthalmologic symptoms and ophthalmologic examination (OE) results in patients with mitochondrial disease