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BACKGROUND Autosomal recessive inborn errors of metabolism often present as life-threatening disease in infancy and have adverse effects on the nervous system. Parents are usually heterozygotes. This is true of most disorders of fatty acid oxidation, which are rare and present with hypoketotic hypoglycemia. However, the gene for medium-chain acyl coenzyme A(More)
Krause CJ. Acinic cell carcinoma: a clinicopatho-logic study of thirty-five cases. We report the unexpected findings of bilateral retinal astrocytic ham-artomas in a giant panda. The eyes of Hsing-Hsing, a giant panda that had renal failure, chronic hyper-tension, degenerative joint disease, and progressive ulcerative keratitis, were examined grossly and(More)
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