Battini R - Search Results

1

Proton magnetic resonance spectroscopy (1H-MRS) of the cerebrum in two young infants with Zellweger syndrome.

Groenendaal F, Bianchi MC, Battini R, Tosetti M, Boldrini A, de Vries LS, Cioni G. Groenendaal F, et al. Among authors: battini r. Neuropediatrics. 2001 Feb;32(1):23-7. doi: 10.1055/s-2001-12218. Neuropediatrics. 2001. PMID: 11315198

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

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

4

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.

5

Prenatal ultrasound and magnetic resonance imaging features in a fetus with Walker-Warburg syndrome.

Strigini F, Valleriani A, Cecchi M, Ghirri P, Aiello C, Bertini E, Cioni G, Battini R. Strigini F, et al. Among authors: battini r. Ultrasound Obstet Gynecol. 2009 Mar;33(3):363-5. doi: 10.1002/uog.6300. Ultrasound Obstet Gynecol. 2009. PMID: 19222032 Free article. No abstract available.

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, neuroradiological and genetic findings in pontocerebellar hypoplasia.

Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, Writzl K, Ventura K, Cheng EY, Ferriero DM, Basel-Vanagaite L, Eggens VR, Krägeloh-Mann I, De Meirleir L, King M, Graham JM Jr, von Moers A, Knoers N, Sztriha L, Korinthenberg R; PCH Consortium; Dobyns WB, Baas F, Poll-The BT. Namavar Y, et al. Brain. 2011 Jan;134(Pt 1):143-56. doi: 10.1093/brain/awq287. Epub 2010 Oct 15. Brain. 2011. PMID: 20952379 Free PMC article.

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

Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study.

Mercuri E, Messina S, Kinali M, Cini C, Longman C, Battini R, Cioni G, Muntoni F. Mercuri E, et al. Among authors: battini r. Neuromuscul Disord. 2004 Feb;14(2):125-9. doi: 10.1016/j.nmd.2003.09.005. Neuromuscul Disord. 2004. PMID: 14733958

10

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

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