Morgese G - Search Results

1

Craniofacial dyssynostosis: case report and review.

Grosso S, Vivarelli R, Muraca MC, Berardi R, Marconcini S, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. Am J Med Genet A. 2004 Sep 1;129A(3):300-2. doi: 10.1002/ajmg.a.30186. Am J Med Genet A. 2004. PMID: 15326632

2

Epilepsy in neurofibromatosis 1.

Vivarelli R, Grosso S, Calabrese F, Farnetani M, Di Bartolo R, Morgese G, Balestri P. Vivarelli R, et al. Among authors: morgese g. J Child Neurol. 2003 May;18(5):338-42. doi: 10.1177/08830738030180050501. J Child Neurol. 2003. PMID: 12822818

3

Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?

Grosso S, Farnetani MA, Berardi R, Vivarelli R, Vanni M, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. Am J Med Genet. 2002 Aug 1;111(2):182-6. doi: 10.1002/ajmg.10493. Am J Med Genet. 2002. PMID: 12210347

4

Medial temporal lobe dysgenesis in Muenke syndrome and hypochondroplasia.

Grosso S, Farnetani MA, Berardi R, Bartalini G, Carpentieri M, Galluzzi P, Mostardini R, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. Am J Med Genet A. 2003 Jul 1;120A(1):88-91. doi: 10.1002/ajmg.a.10171. Am J Med Genet A. 2003. PMID: 12794698

5

Electroencephalographic and epileptic patterns in X chromosome anomalies.

Grosso S, Farnetani MA, Di Bartolo RM, Berardi R, Pucci L, Mostardini R, Anichini C, Bartalini G, Galimberti D, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. J Clin Neurophysiol. 2004 Jul-Aug;21(4):249-53. doi: 10.1097/00004691-200407000-00003. J Clin Neurophysiol. 2004. PMID: 15509914

6

Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature.

Grosso S, Cerase A, De Stefano N, Marco LD, Galluzzi P, Galimberti D, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. Brain Dev. 2005 Jan;27(1):73-7. doi: 10.1016/j.braindev.2004.04.009. Brain Dev. 2005. PMID: 15626547 Review.

7

Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa.

Grosso S, Mostadini R, Cioni M, Galluzzi P, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. J Neurol. 2002 May;249(5):596-600. doi: 10.1007/s004150200069. J Neurol. 2002. PMID: 12021950

8

De novo complete trisomy 5p: clinical and neuroradiological findings.

Grosso S, Cioni M, Garibaldi G, Pucci L, Galluzzi P, Canapicchi R, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. Am J Med Genet. 2002 Sep 15;112(1):56-60. doi: 10.1002/ajmg.10679. Am J Med Genet. 2002. PMID: 12239721

9

Ethylmalonic encephalopathy: further clinical and neuroradiological characterization.

Grosso S, Mostardini R, Farnetani MA, Molinelli M, Berardi R, Dionisi-Vici C, Rizzo C, Morgese G, Balestri P. Grosso S, et al. Among authors: morgese g. J Neurol. 2002 Oct;249(10):1446-50. doi: 10.1007/s00415-002-0880-4. J Neurol. 2002. PMID: 12382164

10

GM2 gangliosidosis variant B1 neuroradiological findings.

Grosso S, Farnetani MA, Berardi R, Margollicci M, Galluzzi P, Vivarelli R, Morgese G, Ballestri P. Grosso S, et al. Among authors: morgese g. J Neurol. 2003 Jan;250(1):17-21. doi: 10.1007/s00415-003-0925-3. J Neurol. 2003. PMID: 12527987

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