Galluzzi P - Search Results

1

Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria.

Vivarelli R, Grosso S, Cioni M, Galluzzi P, Monti L, Morgese G, Balestri P. Vivarelli R, et al. Among authors: galluzzi p. Brain Dev. 2001 Mar;23(1):18-23. doi: 10.1016/s0387-7604(00)00188-1. Brain Dev. 2001. PMID: 11226724

2

MRI Features for Identifying MYCN-amplified RB1 Wild-type Retinoblastoma.

Jansen RW, de Bloeme CM, Cardoen L, Göricke S, van Elst S, Jessen JL, Ramasubramanian A, Skalet AH, Miller AK, Maeder P, Uner OE, Hubbard GB, Grossniklaus H, Boldt HC, Nichols KE, Brennan RC, Sen S, Sirin S, Brisse HJ, Galluzzi P, Dommering CJ, Castelijns JA, van der Valk P, Boellaard R, Dorsman J, Moll AC, de Jong MC, de Graaf P. Jansen RW, et al. Among authors: galluzzi p. Radiology. 2023 Jun;307(5):e222264. doi: 10.1148/radiol.222264. Epub 2023 May 16. Radiology. 2023. PMID: 37191489 Free PMC article.

3

Celiac disease with cerebral calcium and silica deposits: x-ray spectroscopic findings, an autopsy study.

Toti P, Balestri P, Cano M, Galluzzi P, Megha T, Farnetani MA, Palmeri ML, Vascotto M, Venturi C, Fois A. Toti P, et al. Among authors: galluzzi p. Neurology. 1996 Apr;46(4):1088-92. doi: 10.1212/wnl.46.4.1088. Neurology. 1996. PMID: 8780097

4

Pathological case of the month. Multifocal Rosai-Dorfman disease of soft tissue.

Zannolli R, Acquaviva A, Polito E, Galluzzi P, Ferrari F, Leoncini L, Luzi P, Morgese G. Zannolli R, et al. Among authors: galluzzi p. Arch Pediatr Adolesc Med. 1999 Nov;153(11):1199-200. doi: 10.1001/archpedi.153.11.1199. Arch Pediatr Adolesc Med. 1999. PMID: 10555727 No abstract available.

5

MR brain imaging of fucosidosis type I.

Galluzzi P, Rufa A, Balestri P, Cerase A, Federico A. Galluzzi P, et al. AJNR Am J Neuroradiol. 2001 Apr;22(4):777-80. AJNR Am J Neuroradiol. 2001. PMID: 11290499 Free PMC article.

6

Coats disease: smaller volume of the affected globe.

Galluzzi P, Venturi C, Cerase A, Vallone IM, Bracco S, Bardelli AM, Hadjistilianou T, Gennari P, Monti L, Filosomi G. Galluzzi P, et al. Radiology. 2001 Oct;221(1):64-9. doi: 10.1148/radiol.2211010017. Radiology. 2001. PMID: 11568322

7

Cranioectodermal dysplasia: a new patient with an inapparent, subtle phenotype.

Zannolli R, Mostardini R, Carpentieri ML, Gatti MG, Galluzzi P, Terrosi Vagnoli P, Giorgetti R, Calvieri S, Morgese G. Zannolli R, et al. Among authors: galluzzi p. Pediatr Dermatol. 2001 Jul-Aug;18(4):332-5. doi: 10.1046/j.1525-1470.2001.01955.x. Pediatr Dermatol. 2001. PMID: 11576410

8

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: galluzzi p. J Neurol. 2002 May;249(5):596-600. doi: 10.1007/s004150200069. J Neurol. 2002. PMID: 12021950

9

Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration.

Zannolli R, Gilman S, Rossi S, Volpi N, Bernini A, Galluzzi P, Galimberti D, Pucci L, D'Ambrosio A, Morgese G, Giannini F. Zannolli R, et al. Among authors: galluzzi p. Arch Neurol. 2002 Aug;59(8):1319-26. doi: 10.1001/archneur.59.8.1319. Arch Neurol. 2002. PMID: 12164731

10

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: galluzzi p. Am J Med Genet. 2002 Sep 15;112(1):56-60. doi: 10.1002/ajmg.10679. Am J Med Genet. 2002. PMID: 12239721

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