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Case of Myhre syndrome with autism and peculiar skin histological findingsTITOMANLIO, L; MARZANO, M. G; ROSSI, E et al.American journal of medical genetics. 2001, Vol 103, Num 2, pp 163-165, issn 0148-7299Article

Upper airway obstructive disease in mucopolysaccharidoses : Polysomnography, computed tomography and nasal endoscopy findingsSANTAMARIA, F; ANDREUCCI, M. V; PARENTI, G et al.Journal of inherited metabolic disease. 2007, Vol 30, Num 5, pp 743-749, issn 0141-8955, 7 p.Article

Enzyme replacement therapy with agalsidase β improves cardiac involvement in Fabry's diseaseSPINELLI, L; PISANI, A; SABBATINI, M et al.Clinical genetics. 2004, Vol 66, Num 2, pp 158-165, issn 0009-9163, 8 p.Article

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