Guazzi G - Search Results

1

Which method is best for an early accurate diagnosis of acute heart failure? Comparison between lung ultrasound, chest X-ray and NT pro-BNP performance: a prospective study.

Sartini S, Frizzi J, Borselli M, Sarcoli E, Granai C, Gialli V, Cevenini G, Guazzi G, Bruni F, Gonnelli S, Pastorelli M. Sartini S, et al. Among authors: guazzi g. Intern Emerg Med. 2017 Sep;12(6):861-869. doi: 10.1007/s11739-016-1498-3. Epub 2016 Jul 11. Intern Emerg Med. 2017. PMID: 27401330

2

Unusual solution to abdominal pain with contrast enhanced ultrasound.

Montemerani S, Castellani L, Guazzi G, Pastorelli M. Montemerani S, et al. Among authors: guazzi g. BMJ Case Rep. 2019 Nov 4;12(11):e230579. doi: 10.1136/bcr-2019-230579. BMJ Case Rep. 2019. PMID: 31690686 Free PMC article.

3

Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy.

Malandrini A, Carrera P, Ciacci G, Gonnelli S, Villanova M, Palmeri S, Vismara L, Brancolini V, Signorini E, Ferrari M, Guazzi GC. Malandrini A, et al. Among authors: guazzi gc. Neurology. 1997 May;48(5):1200-3. doi: 10.1212/wnl.48.5.1200. Neurology. 1997. PMID: 9153443

4

CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic study.

Malandrini A, Galli L, Villanova M, Palmeri S, Parrotta E, DeFalco D, Cappelli M, Grieco GS, Renieri A, Guazzi G. Malandrini A, et al. Among authors: guazzi g. Eur Neurol. 1998 Oct;40(3):164-8. doi: 10.1159/000007974. Eur Neurol. 1998. PMID: 9748675

5

Type I sialidosis: a clinical, biochemical and neuroradiological study.

Palmeri S, Villanova M, Malandrini A, van Diggelen OP, Huijmans JG, Ceuterick C, Rufa A, DeFalco D, Ciacci G, Martin JJ, Guazzi G. Palmeri S, et al. Among authors: guazzi g. Eur Neurol. 2000;43(2):88-94. doi: 10.1159/000008141. Eur Neurol. 2000. PMID: 10686466

6

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy.

Malandrini A, Carrera P, Palmeri S, Cavallaro T, Fabrizi GM, Villanova M, Fattapposta M, Vismara L, Brancolini V, Tanganelli P, Calì A, Morocutti C, Zeviani M, Ferrari M, Guazzi GC. Malandrini A, et al. Among authors: guazzi gc. Acta Neuropathol. 1996 Aug;92(2):115-22. doi: 10.1007/s004010050498. Acta Neuropathol. 1996. PMID: 8841656

7

Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome?

Guazzi G, Palmeri S, Malandrini A, Ciacci G, Di Perri R, Mancini G, Messina C, Salvadori C. Guazzi G, et al. Am J Med Genet. 1994 Mar 1;50(1):79-83. doi: 10.1002/ajmg.1320500117. Am J Med Genet. 1994. PMID: 8160757

8

The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.

Fabrizi GM, Cardaioli E, Grieco GS, Cavallaro T, Malandrini A, Manneschi L, Dotti MT, Federico A, Guazzi G. Fabrizi GM, et al. Among authors: guazzi g. J Neurol Neurosurg Psychiatry. 1996 Jul;61(1):47-51. doi: 10.1136/jnnp.61.1.47. J Neurol Neurosurg Psychiatry. 1996. PMID: 8676159 Free PMC article.

9

The clinical aspects of adult hexosaminidase deficiencies.

Federico A, Palmeri S, Malandrini A, Fabrizi G, Mondelli M, Guazzi GC. Federico A, et al. Among authors: guazzi gc. Dev Neurosci. 1991;13(4-5):280-7. doi: 10.1159/000112174. Dev Neurosci. 1991. PMID: 1840098 Review.

10

Giant axonal neuropathy in 2 siblings: a generalized disorder of intermediate filaments.

Guazzi GC, Malandrini A, Gerli R, Federico A. Guazzi GC, et al. Eur Neurol. 1991;31(1):50-6. doi: 10.1159/000116646. Eur Neurol. 1991. PMID: 2015839

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