Frattini D - Search Results

1

Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update.

Spagnoli C, Iodice A, Salerno GG, Frattini D, Bertani G, Fusco C. Spagnoli C, et al. Among authors: frattini d. Neuromuscul Disord. 2016 Jun;26(6):394. doi: 10.1016/j.nmd.2016.04.007. Epub 2016 Apr 8. Neuromuscul Disord. 2016. PMID: 27137093 No abstract available.

2

Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes.

Ambrosetti I, Bernardini L, Pollazzon M, Giuffrida MG, Guida V, Peluso F, Baroni MC, Polizzi V, Napoli M, Rosato S, Trimarchi G, Gelmini C, Caraffi SG, Wischmeijer A, Frattini D, Novelli A, Garavelli L. Ambrosetti I, et al. Among authors: frattini d. Genes (Basel). 2023 Jul 26;14(8):1526. doi: 10.3390/genes14081526. Genes (Basel). 2023. PMID: 37628577 Free PMC article. Review.

3

Isolated vitamin E deficiency mimicking distal hereditary motor neuropathy in a 13-year-old boy.

Fusco C, Frattini D, Pisani F, Gellera C, Della Giustina E. Fusco C, et al. Among authors: frattini d. J Child Neurol. 2008 Nov;23(11):1328-30. doi: 10.1177/0883073808318058. J Child Neurol. 2008. PMID: 18984846

4

Congenital pes cavus in a Charcot-Marie-tooth disease type 1A newborn.

Fusco C, Frattini D, Scarano A, Giustina ED. Fusco C, et al. Among authors: frattini d. Pediatr Neurol. 2009 Jun;40(6):461-4. doi: 10.1016/j.pediatrneurol.2008.12.010. Pediatr Neurol. 2009. PMID: 19433282

5

Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation.

Fusco C, Frattini D, Farnetti E, Nicoli D, Casali B, Fiorentino F, Nuccitelli A, Giustina ED. Fusco C, et al. Among authors: frattini d. Brain Dev. 2010 Aug;32(7):592-4. doi: 10.1016/j.braindev.2009.08.003. Epub 2009 Sep 6. Brain Dev. 2010. PMID: 19735987

6

Transient basal ganglia and thalamic involvement following Mycoplasma pneumoniae infection associated with antiganglioside antibodies.

Fusco C, Bonini E, Soncini G, Frattini D, Giovannini S, Della Giustina E. Fusco C, et al. Among authors: frattini d. J Child Neurol. 2010 Aug;25(8):1029-33. doi: 10.1177/0883073809355823. Epub 2010 Mar 19. J Child Neurol. 2010. PMID: 20305125

7

Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient.

Fusco C, Frattini D, Pisani F, Spaggiari F, Ferlini A, Della Giustina E. Fusco C, et al. Among authors: frattini d. J Child Neurol. 2010 Jun;25(6):759-63. doi: 10.1177/0883073809344119. Epub 2010 Apr 9. J Child Neurol. 2010. PMID: 20382840

8

Early onset methylmalonic aciduria and homocystinuria cblC type with demyelinating neuropathy.

Frattini D, Fusco C, Ucchino V, Tavazzi B, Della Giustina E. Frattini D, et al. Pediatr Neurol. 2010 Aug;43(2):135-8. doi: 10.1016/j.pediatrneurol.2010.04.007. Pediatr Neurol. 2010. PMID: 20610126

9

Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome.

Giovannini S, Frattini D, Scarano A, Fusco C, Bertani G, Della Giustina E, Martinelli P, Orteschi D, Zollino M, Neri G, Gobbi G. Giovannini S, et al. Among authors: frattini d. Epileptic Disord. 2010 Sep;12(3):222-7. doi: 10.1684/epd.2010.0324. Epub 2010 Jul 19. Epileptic Disord. 2010. PMID: 20643614 Free article.

10

Cerebellar atrophy in a child with hereditary methemoglobinemia type II.

Fusco C, Soncini G, Frattini D, Della Giustina E, Vercellati C, Fermo E, Bianchi P. Fusco C, et al. Among authors: frattini d. Brain Dev. 2011 Apr;33(4):357-60. doi: 10.1016/j.braindev.2010.06.015. Epub 2010 Jul 22. Brain Dev. 2011. PMID: 20650578

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