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Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients.
Epilepsy Res. 2014 Nov;108(9):1597-603. doi: 10.1016/j.eplepsyres.2014.08.006. Epub 2014 Aug 30.
Epilepsy Res. 2014.
PMID: 25218893
Ketogenic diet in early myoclonic encephalopathy due to non ketotic hyperglycinemia.
Cusmai R, Martinelli D, Moavero R, Dionisi Vici C, Vigevano F, Castana C, Elia M, Bernabei S, Bevivino E.
Cusmai R, et al. Among authors: bevivino e.
Eur J Paediatr Neurol. 2012 Sep;16(5):509-13. doi: 10.1016/j.ejpn.2011.12.015. Epub 2012 Jan 18.
Eur J Paediatr Neurol. 2012.
PMID: 22261077
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Lyonization effects of the t(X;16) translocation on the phenotypic expression in a rare female with Menkes disease.
Sirleto P, Surace C, Santos H, Bertini E, Tomaiuolo AC, Lombardo A, Boenzi S, Bevivino E, Dionisi-Vici C, Angioni A.
Sirleto P, et al. Among authors: bevivino e.
Pediatr Res. 2009 Mar;65(3):347-51. doi: 10.1203/PDR.0b013e3181973b4e.
Pediatr Res. 2009.
PMID: 19092723
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LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance.
Dallabona C, Abbink TE, Carrozzo R, Torraco A, Legati A, van Berkel CG, Niceta M, Langella T, Verrigni D, Rizza T, Diodato D, Piemonte F, Lamantea E, Fang M, Zhang J, Martinelli D, Bevivino E, Dionisi-Vici C, Vanderver A, Philip SG, Kurian MA, Verma IC, Bijarnia-Mahay S, Jacinto S, Furtado F, Accorsi P, Ardissone A, Moroni I, Ferrero I, Tartaglia M, Goffrini P, Ghezzi D, van der Knaap MS, Bertini E.
Dallabona C, et al. Among authors: bevivino e.
Brain. 2016 Mar;139(Pt 3):782-94. doi: 10.1093/brain/awv392. Epub 2016 Jan 29.
Brain. 2016.
PMID: 26912632
Free article.
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Immunodeficiency in Vici syndrome: a heterogeneous phenotype.
Finocchi A, Angelino G, Cantarutti N, Corbari M, Bevivino E, Cascioli S, Randisi F, Bertini E, Dionisi-Vici C.
Finocchi A, et al. Among authors: bevivino e.
Am J Med Genet A. 2012 Feb;158A(2):434-9. doi: 10.1002/ajmg.a.34244. Epub 2011 Sep 30.
Am J Med Genet A. 2012.
PMID: 21965116
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Understanding pyrroline-5-carboxylate synthetase deficiency: clinical, molecular, functional, and expression studies, structure-based analysis, and novel therapy with arginine.
Martinelli D, Häberle J, Rubio V, Giunta C, Hausser I, Carrozzo R, Gougeard N, Marco-Marín C, Goffredo BM, Meschini MC, Bevivino E, Boenzi S, Colafati GS, Brancati F, Baumgartner MR, Dionisi-Vici C.
Martinelli D, et al. Among authors: bevivino e.
J Inherit Metab Dis. 2012 Sep;35(5):761-76. doi: 10.1007/s10545-011-9411-8. Epub 2011 Dec 15.
J Inherit Metab Dis. 2012.
PMID: 22170564
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Neuroradiologic Phenotyping of Galactosemia: From the Neonatal Form to the Chronic Stage.
Rossi-Espagnet MC, Sudhakar S, Fontana E, Longo D, Davison J, Petengill AL, Bevivino E, Pacheco FT, da Rocha AJ, Hanagandi P, Soldatelli M, Mankad K, do Amaral LLF.
Rossi-Espagnet MC, et al. Among authors: bevivino e.
AJNR Am J Neuroradiol. 2021 Mar;42(3):590-596. doi: 10.3174/ajnr.A7016. Epub 2021 Jan 21.
AJNR Am J Neuroradiol. 2021.
PMID: 33478945
Free PMC article.
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Duodenal stenosis, a new finding on congenital rubella syndrome: case description and literature review.
Diamanti A, Pietrobattista A, Bevivino E, De Angelis P, Calce A, Dall'Oglio L, Gambarara M.
Diamanti A, et al. Among authors: bevivino e.
J Infect. 2006 Nov;53(5):e207-10. doi: 10.1016/j.jinf.2006.01.020. Epub 2006 Mar 20.
J Infect. 2006.
PMID: 16546260
Review.
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