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Zespół Kogana został zgłoszony jako związany z zapaleniem rogówki i dysfunkcją przedsionkową przez Cogan w 1945 roku. Większość z nich ma objawy ogólnoustrojowe, takie jak gorączka, choroby serca, zaburzenia trawienia, bóle stawów i eozynofilia. Uważa się, że jest podtypem zapalenia wielolistnego.
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코간증후군 w następujących pozycjach bibliograficznych Książki powiązane ze słowem
코간증후군 oraz krótkie ich fragmenty w celu przedstawienia kontekstu użycia w literaturze.
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