코간증후군在韩语中的意思是什么？
在韩语 词典里코간증후군的定义
据报道，Kogan综合征与科根在1945年发生的角膜炎和前庭功能障碍有关。 他们大多数有全身症状，如发烧，心脏病，消化系统疾病，关节痛和嗜酸性粒细胞增多。 它被认为是多动脉炎的一种亚型。 코간증후군 1945년 Cogan에 의해서 각막염과 전정(前庭) 기능부전을 수반하는 것으로서 발표되었다. 그 대부분은 발열, 심질환, 소화계 이상, 관절통, 호산구증다 등 전신증상을 나타난다. 다발성 동맥염의 아형으로도 생각되고 있다.
与 «코간증후군»相关的韩语书籍
在以下的参考文献中发现
코간증후군的用法。与
코간증후군相关的书籍以及同一来源的简短摘要提供其在 韩语文献中的使用情境。
1
Visual Processing Deficits in the Fragile X Syndrome
A series of empirical studies is presented that examine the contribution of Fragile X Mental Retardation 1 (FMR1) gene expression to the structure and function of the visual system.
2
Neurogenetic Developmental Disorders: Variation of ... - 89페이지
Visual–Motor Coordination Another striking aspect of fragile X syndrome is the observed visuomotor deficits. ... One possible explanation for this dissociation has come from a series of recent neurobiological studies by Kogan and colleagues ...
Michèle M. M. Mazzocco, Judith L. Ross, 2007
3
Eye Gaze and Shifting Behaviors in Infants with Fragile X ... - 8페이지
Neurobiology of fragile X syndrome In order to understand the relationship between behavioral abnormalities and the underlying causes of fragile X ... In a study by Kogan and colleagues (2004), adult and adolescent males underwent a ...
Rashelle Jean Musci, 2008
4
New Research on Fragile X Syndrome - 31페이지
[42,43] One possible explanation for this dissociation has come from a series of recent neurobiological studies by Kogan and colleagues that speculate that FXS is associated with selective deficits in magnocellular/dorsal stream visual ...
5
Modeling Fragile X Syndrome - 267페이지
J Intellect Disabil Res 52:469–482 Cornish KM, Li L, Kogan CS, Jacquemont S, Turk J, Dalton A, Hagerman RJ, Hagerman PJ (2008b) Age-dependent cognitive changes in carriers of the fragile X syndrome. Cortex 44:628–636 Cornish KM, ...
6
Pediatric Nephrology - 617페이지
Ismaili K, Verdure V, Vandenhoute K, Janssen F, Hall M. WT1 gene mutations in three girls with nephrotic syndrome. ... VanDeVoorde R, Witte D, Kogan J, Goebel J. Pierson syndrome: a novel cause of congenital nephrotic syndrome.
Ellis D. Avner, William E. Harmon, Patrick Niaudet, 2009
Nalin Gupta, Anuradha Banerjee, Daphne Haas-Kogan. To identify retinal angiomas, ophthalmologic ... SturgeWeber syndrome (SWS), or encephalofacial angiomatosis, occurs sporadically. It is a readily recognizable congenital disorder with ...
Nalin Gupta, Anuradha Banerjee, Daphne Haas-Kogan, 2013
8
Visual Diagnosis and Care of the Patient with Special Needs - 47페이지
2002;44:724–8. Storm RL, PeBenito R, Ferretti C. Ophthalmologic findings in the fragile X syndrome. Arch Ophthalmol. ... Kogan CS, Bertone A, Cornish K, Boutet I, Der Kaloustian VM, Andermann E, et al. Integrative cortical dysfunction and ...
Marc B. Taub, Mary Bartuccio, Dominick Maino, 2012
9
Neurodevelopmental Disorders Across the Lifespan: A ... - 360페이지
Block design performance in the Williams syndrome phenotype: a problem with mental imagery? Journal of Child Psychology ... Cortex, 39, 161–63. Kogan, C.S., Bertone, A., Cornish, K., Boutet, I., Der Kaloustian, V.M., Andermann, E., et al.
Emily K. Farran, Annette Karmiloff-Smith, 2011
10
Handbook of Pediatric Urology - 159페이지
Laurence S. Baskin, Barry A. Kogan .*.*, * ... Syndrome). Ronald S. Sutherland URACHAL ANOMALIES (Fig. 16-1) A. Background. The urachus is a fibrous band that extends from the anterior bladder wall to the umbilicus as the remnant of the ...
Laurence S. Baskin, Barry A. Kogan, 2005
