Battaglia D - Search Results

1

Hypoventilation in REM sleep in a case of 17p11.2 deletion (Smith-Magenis syndrome).

Leoni C, Cesarini L, Dittoni S, Battaglia D, Novelli A, Bernardini L, Losurdo A, Vollono C, Testani E, Della Marca G, Zampino G. Leoni C, et al. Among authors: battaglia d. Am J Med Genet A. 2010 Mar;152A(3):708-12. doi: 10.1002/ajmg.a.32700. Am J Med Genet A. 2010. PMID: 20186811

2

Electroclinical patterns and evolution of epilepsy in the 4p- syndrome.

Battaglia D, Zampino G, Zollino M, Mariotti P, Acquafondata C, Lettori D, Pane M, Vasta I, Neri G, Dravet C, Guzzetta F. Battaglia D, et al. Epilepsia. 2003 Sep;44(9):1183-90. doi: 10.1046/j.1528-1157.2003.63502.x. Epilepsia. 2003. PMID: 12919390 Free article.

3

Epilepsy in shunted posthemorrhagic infantile hydrocephalus owing to pre- or perinatal intra- or periventricular hemorrhage.

Battaglia D, Pasca MG, Cesarini L, Tartaglione T, Acquafondata C, Randò T, Veredice C, Ricci D, Guzzetta F. Battaglia D, et al. J Child Neurol. 2005 Mar;20(3):219-25. doi: 10.1177/08830738050200030901. J Child Neurol. 2005. PMID: 15832612

4

Developmental plasticity after right hemispherectomy in an epileptic adolescent with early brain injury.

Chiricozzi F, Chieffo D, Battaglia D, Iuvone L, Acquafondata C, Cesarini L, Sacco A, Chiera R, Di Rocco C, Guzzetta F. Chiricozzi F, et al. Among authors: battaglia d. Childs Nerv Syst. 2005 Nov;21(11):960-9. doi: 10.1007/s00381-005-1148-y. Epub 2005 Apr 26. Childs Nerv Syst. 2005. PMID: 15856259

5

Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.

Zollino M, Lecce R, Murdolo M, Orteschi D, Marangi G, Selicorni A, Midro A, Sorge G, Zampino G, Memo L, Battaglia D, Petersen M, Pandelia E, Gyftodimou Y, Faravelli F, Tenconi R, Garavelli L, Mazzanti L, Fischetto R, Cavalli P, Savasta S, Rodriguez L, Neri G. Zollino M, et al. Among authors: battaglia d. Hum Genet. 2007 Dec;122(5):423-30. doi: 10.1007/s00439-007-0412-5. Epub 2007 Aug 4. Hum Genet. 2007. PMID: 17676343

6

Giant subcortical heterotopia involving the temporo-parieto-occipital region: a challenging cause of drug-resistant epilepsy.

Novegno F, Battaglia D, Chieffo D, Frassanito P, Leoni C, Tamburrini G, Massimi L, Tartaglione T, Di Rocco C, Guzzetta F. Novegno F, et al. Among authors: battaglia d. Epilepsy Res. 2009 Nov;87(1):88-94. doi: 10.1016/j.eplepsyres.2009.06.006. Epub 2009 Jul 19. Epilepsy Res. 2009. PMID: 19619986

7

Visual and visuoperceptual function in children with Panayiotopoulos syndrome.

De Rose P, Perrino F, Lettori D, Alfieri P, Cesarini L, Battaglia D, Ricci D, Guzzetta F, Mercuri E. De Rose P, et al. Among authors: battaglia d. Epilepsia. 2010 Jul;51(7):1205-11. doi: 10.1111/j.1528-1167.2009.02484.x. Epub 2010 Jan 7. Epilepsia. 2010. PMID: 20067504 Free article.

8

Increased sleep spindle activity in patients with Costello syndrome (HRAS gene mutation).

Della Marca G, Leoni C, Dittoni S, Battaglia D, Losurdo A, Testani E, Colicchio S, Gnoni V, Gambardella ML, Mariotti P, Alfieri P, Tartaglia M, Zampino G. Della Marca G, et al. Among authors: battaglia d. J Clin Neurophysiol. 2011 Jun;28(3):314-8. doi: 10.1097/WNP.0b013e31821c3ad5. J Clin Neurophysiol. 2011. PMID: 21633259

9

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.

Zollino M, Orteschi D, Murdolo M, Lattante S, Battaglia D, Stefanini C, Mercuri E, Chiurazzi P, Neri G, Marangi G. Zollino M, et al. Among authors: battaglia d. Nat Genet. 2012 Apr 29;44(6):636-8. doi: 10.1038/ng.2257. Nat Genet. 2012. PMID: 22544367

10

Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions.

Onesimo R, Orteschi D, Scalzone M, Rossodivita A, Nanni L, Zannoni GF, Marrocco G, Battaglia D, Fundarò C, Neri G. Onesimo R, et al. Among authors: battaglia d. Am J Med Genet A. 2012 Sep;158A(9):2266-71. doi: 10.1002/ajmg.a.35489. Epub 2012 Jul 20. Am J Med Genet A. 2012. PMID: 22821627

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