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21 results on '"Valenti, Maria"'

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1. Expression of FBXW11 in normal and disease‐associated osteogenic cells

8. Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: Genomic dissection makes the link with autism

9. Lack of expression ofSERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen

14. Eyelid fluttering, typical EEG pattern, and impaired intellectual function: A homogeneous epileptic condition among the patients presenting with eyelid myoclonia

21. Isolated paroxysmal arousals as focal epilepsy.

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