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Page 1
Pharmacologic treatment of hyperthyroidism during pregnancy.
Cassina M, Donà M, Di Gianantonio E, Clementi M. Cassina M, et al. Among authors: dona m. Birth Defects Res A Clin Mol Teratol. 2012 Aug;94(8):612-9. doi: 10.1002/bdra.23012. Epub 2012 Apr 18. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22511519 Review.
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.
Cao M, Donà M, Valentino ML, Valentino L, Semplicini C, Maresca A, Cassina M, Torraco A, Galletta E, Manfioli V, Sorarù G, Carelli V, Stramare R, Bertini E, Carrozzo R, Salviati L, Pegoraro E. Cao M, et al. Among authors: dona m. Neurogenetics. 2016 Jan;17(1):65-70. doi: 10.1007/s10048-015-0465-x. Epub 2015 Nov 10. Neurogenetics. 2016. PMID: 26556812
Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.
Cao M, Donà M, Valentino ML, Semplicini C, Maresca A, Cassina M, Torraco A, Galletta E, Manfioli V, Sorarù G, Carelli V, Stramare R, Bertini E, Carozzo R, Salviati L, Pegoraro E. Cao M, et al. Among authors: dona m. Neurogenetics. 2016 Apr;17(2):143. doi: 10.1007/s10048-016-0475-3. Neurogenetics. 2016. PMID: 26924555 No abstract available.
Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.
Cao M, Donà M, Lucia Valentino M, Semplicini C, Maresca A, Cassina M, Torraco A, Galletta E, Manfioli V, Sorarù G, Carelli V, Stramare R, Bertini E, Carrozzo R, Salviati L, Pegoraro E. Cao M, et al. Among authors: dona m. Neurogenetics. 2017 Jan;18(1):69. doi: 10.1007/s10048-016-0501-5. Neurogenetics. 2017. PMID: 27913898 No abstract available.
6q27 subtelomeric deletions: Is there a specific phenotype?
Rigon C, Salviati L, Mandarano R, Donà M, Clementi M. Rigon C, et al. Among authors: dona m. Am J Med Genet A. 2011 May;155A(5):1213-4. doi: 10.1002/ajmg.a.33877. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484997 No abstract available.
197 results