Deodato F - Search Results

1

Epileptic negative myoclonus in a newborn with hemimegalencephaly.

Guzzetta F, Battaglia D, Lettori D, Deodato F, Sani E, Randò T, Ricci D, Acquafondata C, Faienza C. Guzzetta F, et al. Among authors: deodato f. Epilepsia. 2002 Sep;43(9):1106-9. doi: 10.1046/j.1528-1157.2002.15001.x. Epilepsia. 2002. PMID: 12199738 Free article.

2

Brain ischemic lesions of the newborn.

Guzzetta F, Deodato F, Randò T. Guzzetta F, et al. Among authors: deodato f. Childs Nerv Syst. 2000 Nov;16(10-11):633-7. doi: 10.1007/s003810000318. Childs Nerv Syst. 2000. PMID: 11151712 Review.

3

Epileptic disorders with onset in the first year of life: neurological and cognitive outcome.

Battaglia D, Randò T, Deodato F, Bruccini G, Baglio G, Frisone MF, Pantò T, Tortorella G, Guzzetta F. Battaglia D, et al. Among authors: deodato f. Eur J Paediatr Neurol. 1999;3(3):95-103. doi: 10.1016/s1090-3798(99)90096-x. Eur J Paediatr Neurol. 1999. PMID: 10461564

4

Assessment of visual function in children with methylmalonic aciduria and homocystinuria.

Ricci D, Pane M, Deodato F, Vasco G, Randò T, Caviglia S, Dionisi-Vici C, Mercuri E. Ricci D, et al. Among authors: deodato f. Neuropediatrics. 2005 Jun;36(3):181-5. doi: 10.1055/s-2005-865609. Neuropediatrics. 2005. PMID: 15944903

5

Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiency.

Deodato F, Sabatelli M, Ricci E, Mercuri E, Muntoni F, Sewry C, Naom I, Tonali P, Guzzetta F. Deodato F, et al. Neuromuscul Disord. 2002 May;12(4):392-8. doi: 10.1016/s0960-8966(01)00312-1. Neuromuscul Disord. 2002. PMID: 12062258

6

Methylmalonic and propionic aciduria.

Deodato F, Boenzi S, Santorelli FM, Dionisi-Vici C. Deodato F, et al. Am J Med Genet C Semin Med Genet. 2006 May 15;142C(2):104-12. doi: 10.1002/ajmg.c.30090. Am J Med Genet C Semin Med Genet. 2006. PMID: 16602092 Review.

7

'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometry.

Dionisi-Vici C, Deodato F, Röschinger W, Rhead W, Wilcken B. Dionisi-Vici C, et al. Among authors: deodato f. J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):383-9. doi: 10.1007/s10545-006-0278-z. J Inherit Metab Dis. 2006. PMID: 16763906 Review.

8

Cobalamin C defect: natural history, pathophysiology, and treatment.

Martinelli D, Deodato F, Dionisi-Vici C. Martinelli D, et al. Among authors: deodato f. J Inherit Metab Dis. 2011 Feb;34(1):127-35. doi: 10.1007/s10545-010-9161-z. Epub 2010 Jul 15. J Inherit Metab Dis. 2011. PMID: 20632110 Review.

9

Successful pregnancy in a woman with mut- methylmalonic acidaemia.

Deodato F, Rizzo C, Boenzi S, Baiocco F, Sabetta G, Dionisi-Vici C. Deodato F, et al. J Inherit Metab Dis. 2002 May;25(2):133-4. doi: 10.1023/a:1015632911801. J Inherit Metab Dis. 2002. PMID: 12118529

10

SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.

Carrozzo R, Dionisi-Vici C, Steuerwald U, Lucioli S, Deodato F, Di Giandomenico S, Bertini E, Franke B, Kluijtmans LA, Meschini MC, Rizzo C, Piemonte F, Rodenburg R, Santer R, Santorelli FM, van Rooij A, Vermunt-de Koning D, Morava E, Wevers RA. Carrozzo R, et al. Among authors: deodato f. Brain. 2007 Mar;130(Pt 3):862-74. doi: 10.1093/brain/awl389. Epub 2007 Feb 14. Brain. 2007. PMID: 17301081

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