Salvestroni R - Search Results

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Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency.

Villanova M, Malandrini A, Toti P, Salvestroni R, Six J, Martin JJ, Guazzi GC. Villanova M, et al. Among authors: salvestroni r. J Submicrosc Cytol Pathol. 1996 Jan;28(1):1-4. J Submicrosc Cytol Pathol. 1996. PMID: 8929621

Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency.

Villanova M, Malandrini A, Biancotti R, Löfgren A, Mongini T, Six J, Salvestroni R, Parrotta E, Van Broeckhoven C, Paolozzi C, Guazzi G. Villanova M, et al. Among authors: salvestroni r. Neuromuscul Disord. 1996 May;6(3):167-72. doi: 10.1016/0960-8966(96)00016-8. Neuromuscul Disord. 1996. PMID: 8784804

Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy.

Malandrini A, Cavallaro T, Fabrizi GM, Berti G, Salvestroni R, Salvadori C, Guazzi GC. Malandrini A, et al. Among authors: salvestroni r. Virchows Arch. 1995;427(4):415-21. doi: 10.1007/BF00199391. Virchows Arch. 1995. PMID: 8548127

An unusual type of primary cerebral hemihypotrophy with signs of dysfunctional neuronal migration.

Malandrini A, Lo Russo F, Villanova M, Salvestroni R, Sicurelli F, Salvadori C, Paolozzi C, Guazzi GC. Malandrini A, et al. Among authors: salvestroni r. Acta Neuropathol. 1996 Dec;92(6):631-4. doi: 10.1007/s004010050572. Acta Neuropathol. 1996. PMID: 8960323

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