Salviati A - Search Results

1

Vascular dementia in a population-based autopsy study.

Knopman DS, Parisi JE, Boeve BF, Cha RH, Apaydin H, Salviati A, Edland SD, Rocca WA. Knopman DS, et al. Among authors: salviati a. Arch Neurol. 2003 Apr;60(4):569-75. doi: 10.1001/archneur.60.4.569. Arch Neurol. 2003. PMID: 12707071

2

Neuropathology of cognitively normal elderly.

Knopman DS, Parisi JE, Salviati A, Floriach-Robert M, Boeve BF, Ivnik RJ, Smith GE, Dickson DW, Johnson KA, Petersen LE, McDonald WC, Braak H, Petersen RC. Knopman DS, et al. Among authors: salviati a. J Neuropathol Exp Neurol. 2003 Nov;62(11):1087-95. doi: 10.1093/jnen/62.11.1087. J Neuropathol Exp Neurol. 2003. PMID: 14656067

3

Inherited neuroaxonal dystrophy in C6 deficient rabbits.

Giannini C, Monaco S, Kirschfink M, Rother KO, Lorbacher de Ruiz H, Nardelli E, Bonetti B, Salviati A, Zanette GP, Rizzuto N. Giannini C, et al. Among authors: salviati a. J Neuropathol Exp Neurol. 1992 Sep;51(5):514-22. doi: 10.1097/00005072-199209000-00006. J Neuropathol Exp Neurol. 1992. PMID: 1517772

4

[Peripheral nerve biopsy. Indications, methods and principal pathological pictures].

Rizzuto N, Moretto G, Monaco S, Simonati A, Salviati A. Rizzuto N, et al. Among authors: salviati a. Riv Neurol. 1988 Mar-Apr;58(2):89-92. Riv Neurol. 1988. PMID: 2845560 Review. Italian. No abstract available.

5

Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological study.

Polo A, Teatini F, D'Anna S, Manganotti P, Salviati A, Dallapiccola B, Zanette G, Rizzuto N. Polo A, et al. Among authors: salviati a. J Neurol. 1996 May;243(5):388-92. doi: 10.1007/BF00868997. J Neurol. 1996. PMID: 8741078

6

Neuroaxonal dystrophy with dystonia and pallidal involvement.

Simonati A, Trevisan C, Salviati A, Rizzuto N. Simonati A, et al. Among authors: salviati a. Neuropediatrics. 1999 Jun;30(3):151-4. doi: 10.1055/s-2007-973482. Neuropediatrics. 1999. PMID: 10480212

7

AZT-induced mitochondrial myopathy.

Tomelleri G, Tonin P, Spadaro M, Tilia G, Orrico D, Barelli A, Bonetti B, Monaco S, Salviati A, Morocutti C, et al. Tomelleri G, et al. Among authors: salviati a. Ital J Neurol Sci. 1992 Dec;13(9):723-8. doi: 10.1007/BF02229156. Ital J Neurol Sci. 1992. PMID: 1336487

8

Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis.

Gomez-Lira M, Moretto G, Bonamini D, Benedetti MD, Pignatti PF, Rizzuto N, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. J Neuroimmunol. 2002 Dec;133(1-2):241-3. doi: 10.1016/s0165-5728(02)00361-2. J Neuroimmunol. 2002. PMID: 12446029

9

A common beta hexosaminidase gene mutation in adult Sandhoff disease patients.

Gomez-Lira M, Sangalli A, Mottes M, Perusi C, Pignatti PF, Rizzuto N, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. Hum Genet. 1995 Oct;96(4):417-22. doi: 10.1007/BF00191799. Hum Genet. 1995. PMID: 7557963

10

Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation and show different phenotypes; description of a novel null-type mutation.

Gomez-Lira M, Perusi C, Mottes M, Pignatti PF, Manfredi M, Rizzuto N, Salviati A. Gomez-Lira M, et al. Among authors: salviati a. Hum Genet. 1998 Apr;102(4):459-63. doi: 10.1007/s004390050721. Hum Genet. 1998. PMID: 9600244

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