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- W2116713889 abstract "Juvenile Paget disease or familial hyperphosphatasia is a rare autosomal recessive disorder, which represents a distinct clinical condition, not simply a juvenile-onset form of Paget disease. Osteoprotegerin deficiency leads to marked osteoclast activation and greatly accelerated bone remodeling. We" @default.
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- W2116713889 date "2007-10-18" @default.
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- W2116713889 title "Bilateral Cavernous Internal Carotid Aneurysms in a Child with Juvenile Paget Disease and Osteoprotegerin Deficiency" @default.
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- W2116713889 doi "https://doi.org/10.3174/ajnr.a0755" @default.
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