Battini R - Search Results

1

Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution.

Fiori S, Poretti A, Pannek K, Del Punta R, Pasquariello R, Tosetti M, Guzzetta A, Rose S, Cioni G, Battini R. Fiori S, et al. Among authors: battini r. AJNR Am J Neuroradiol. 2016 May;37(5):917-23. doi: 10.3174/ajnr.A4607. Epub 2015 Dec 10. AJNR Am J Neuroradiol. 2016. PMID: 26659337 Free PMC article.

2

Brain lactic alkalosis in Aicardi-Goutières syndrome.

Robertson NJ, Stafler P, Battini R, Cheong J, Tosetti M, Bianchi MC, Cox IJ, Cowan FM, Cioni G. Robertson NJ, et al. Among authors: battini r. Neuropediatrics. 2004 Feb;35(1):20-6. doi: 10.1055/s-2004-815787. Neuropediatrics. 2004. PMID: 15002048

3

Characterization of the phenotype and definition of the deletion in a new patient with ring chromosome 22.

Battini R, Battaglia A, Bertini V, Cioni G, Parrini B, Rapalini E, Simi P, Tinelli F, Valetto A. Battini R, et al. Am J Med Genet A. 2004 Oct 1;130A(2):196-9. doi: 10.1002/ajmg.a.30276. Am J Med Genet A. 2004. PMID: 15372517

4

Early assessment of visual information processing and neurological outcome in preterm infants.

Guzzetta A, Mazzotti S, Tinelli F, Bancale A, Ferretti G, Battini R, Bartalena L, Boldrini A, Cioni G. Guzzetta A, et al. Among authors: battini r. Neuropediatrics. 2006 Oct;37(5):278-85. doi: 10.1055/s-2006-955929. Neuropediatrics. 2006. PMID: 17236106

5

Treatment monitoring of brain creatine deficiency syndromes: a 1H- and 31P-MR spectroscopy study.

Bianchi MC, Tosetti M, Battini R, Leuzzi V, Alessandri' MG, Carducci C, Antonozzi I, Cioni G. Bianchi MC, et al. Among authors: battini r. AJNR Am J Neuroradiol. 2007 Mar;28(3):548-54. AJNR Am J Neuroradiol. 2007. PMID: 17353334 Free PMC article. Clinical Trial.

6

Muscle MRI in FHL1-linked reducing body myopathy.

Astrea G, Schessl J, Clement E, Tosetti M, Mercuri E, Rutherford M, Cioni G, Bönnemann CG, Muntoni F, Battini R. Astrea G, et al. Among authors: battini r. Neuromuscul Disord. 2009 Oct;19(10):689-91. doi: 10.1016/j.nmd.2009.06.372. Epub 2009 Jul 17. Neuromuscul Disord. 2009. PMID: 19616434

7

Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia.

Battini R, Fogli A, Borghetti D, Michelucci A, Perazza S, Baldinotti F, Conidi ME, Ferreri MI, Simi P, Cioni G. Battini R, et al. Eur J Neurol. 2011 Jan;18(1):150-7. doi: 10.1111/j.1468-1331.2010.03102.x. Eur J Neurol. 2011. PMID: 20550563

8

Language disorder with mild intellectual disability in a child affected by a novel mutation of SLC6A8 gene.

Battini R, Chilosi AM, Casarano M, Moro F, Comparini A, Alessandrì MG, Leuzzi V, Tosetti M, Cioni G. Battini R, et al. Mol Genet Metab. 2011 Feb;102(2):153-6. doi: 10.1016/j.ymgme.2010.11.005. Epub 2010 Nov 13. Mol Genet Metab. 2011. PMID: 21144783

9

Muscle MRI in TRPV4-related congenital distal SMA.

Astrea G, Brisca G, Fiorillo C, Valle M, Tosetti M, Bruno C, Santorelli FM, Battini R. Astrea G, et al. Among authors: battini r. Neurology. 2012 Jan 31;78(5):364-5. doi: 10.1212/WNL.0b013e318245295a. Neurology. 2012. PMID: 22291064 No abstract available.

10

Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency.

Casarano M, Alessandrì MG, Salomons GS, Moretti E, Jakobs C, Gibson KM, Cioni G, Battini R. Casarano M, et al. Among authors: battini r. JIMD Rep. 2012;2:119-23. doi: 10.1007/8904_2011_60. Epub 2011 Sep 6. JIMD Rep. 2012. PMID: 23430864 Free PMC article.

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