Salvadori C - Search Results

1

DNA end labelling (TUNEL) in a 3 year old girl with Leigh syndrome and prevalent cortical involvement.

Formichi P, Malandrini A, Battisti C, Santorelli FM, Gambelli S, Tripodi SA, Berti G, Salvadori C, Tessa A, Federico A. Formichi P, et al. Among authors: salvadori c. J Neurol Neurosurg Psychiatry. 2004 Jun;75(6):930-2. doi: 10.1136/jnnp.2003.016410. J Neurol Neurosurg Psychiatry. 2004. PMID: 15146020 Free PMC article.

2

Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report.

Malandrini A, Palmeri S, Fabrizi GM, Villanova M, Berti G, Salvadori C, Gardini G, Motti L, Solimé F, Guazzi GC. Malandrini A, et al. Among authors: salvadori c. J Neurol Sci. 1998 Mar 5;155(2):218-21. doi: 10.1016/s0022-510x(98)00014-8. J Neurol Sci. 1998. PMID: 9562272

3

Neuronal intranuclear inclusion disease: neuropathologic study of a case.

Malandrini A, Villanova M, Tripodi S, Palmeri S, Sicurelli F, Parrotta E, Berti G, Salvadori C, Cintorino M, Guazzi GC. Malandrini A, et al. Among authors: salvadori c. Brain Dev. 1998 Aug;20(5):290-4. doi: 10.1016/s0387-7604(98)00032-1. Brain Dev. 1998. PMID: 9760997

4

Neuropathological findings associated with retained lead shot pellets in a man surviving two months after a suicide attempt.

Malandrini A, Villanova M, Salvadori C, Gambelli S, Berti G, Di Paolo M. Malandrini A, et al. Among authors: salvadori c. J Forensic Sci. 2001 May;46(3):717-21. J Forensic Sci. 2001. PMID: 11373015

5

Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy.

Gambelli S, Malandrini A, Ginanneschi F, Berti G, Cardaioli E, De Stefano R, Franci M, Salvadori C, Mari F, Bruttini M, Rossi A, Federico A, Renieri A. Gambelli S, et al. Among authors: salvadori c. Eur Neurol. 2004;51(3):144-7. doi: 10.1159/000077070. Epub 2004 Feb 27. Eur Neurol. 2004. PMID: 14988608

6

A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal course.

Malandrini A, Luchini D, Gambelli S, Gaudiano C, Berti G, Salvadori C, Serni G, Valassina M, Federico A, Di Paolo M. Malandrini A, et al. Among authors: salvadori c. J Clin Forensic Med. 2004 Aug;11(4):208-10. doi: 10.1016/j.jcfm.2004.04.009. J Clin Forensic Med. 2004. PMID: 15363755

7

Typical pathological changes of CADASIL in the optic nerve.

Rufa A, Malandrini A, Dotti MT, Berti G, Salvadori C, Federico A. Rufa A, et al. Among authors: salvadori c. Neurol Sci. 2005 Oct;26(4):271-4. doi: 10.1007/s10072-005-0470-1. Neurol Sci. 2005. PMID: 16193254

8

A new missense mutation in caveolin-3 gene causes rippling muscle disease.

Dotti MT, Malandrini A, Gambelli S, Salvadori C, De Stefano N, Federico A. Dotti MT, et al. Among authors: salvadori c. J Neurol Sci. 2006 Apr 15;243(1-2):61-4. doi: 10.1016/j.jns.2005.11.032. Epub 2006 Feb 3. J Neurol Sci. 2006. PMID: 16458928

9

Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 cases.

Malandrini A, Selvi E, Villanova M, Berti G, Sabadini L, Salvadori C, Gambelli S, De Stefano R, Vernillo R, Marcolongo R, Guazzi G. Malandrini A, et al. Among authors: salvadori c. J Rheumatol. 2000 May;27(5):1203-6. J Rheumatol. 2000. PMID: 10813288

10

Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus.

Malandrini A, Fabrizi GM, Palmeri S, Ciacci G, Salvadori C, Berti G, Bucalossi A, Federico A, Guazzi GC. Malandrini A, et al. Among authors: salvadori c. Acta Neuropathol. 1993;86(6):651-8. doi: 10.1007/BF00294306. Acta Neuropathol. 1993. PMID: 8310821

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