Knobloch syndrome is an autosomal recessive developmental disorder primarily characterized by typical eye abnormalities, including high myopia, cataracts, dislocated lens, vitreoretinal degeneration, and retinal detachment, with occipital skull defects, which can range from occipital encephalocele to occult cutis aplasia (summary by Aldahmesh et al., 2011).
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get priceMar 15, 2017· Recovery after Acute Kidney Injury. Kellum JA(1)(2), Sileanu FE(1)(2), Bihorac A(3), Hoste EA(4), Chawla LS(5). Author information: (1)1 The Center for Critical Care Nephology, Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
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get priceApr 29, 2012· 1. Nature. 2012 Apr 29;485(7399):517-21. doi: 10.1038/nature11007. Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity.
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