Villanova M - Search Results

1

Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markers.

Villanova M, Kawai M, Lübke U, Oh SJ, Perry G, Six J, Ceuterick C, Martin JJ, Cras P. Villanova M, et al. Brain Res. 1993 Feb 19;603(2):343-7. doi: 10.1016/0006-8993(93)91260-y. Brain Res. 1993. PMID: 8461987

2

Microtubule-associated protein tau epitopes are present in fiber lesions in diverse muscle disorders.

Lübke U, Six J, Villanova M, Boons J, Vandermeeren M, Ceuterick C, Cras P, Martin JJ. Lübke U, et al. Among authors: villanova m. Am J Pathol. 1994 Jul;145(1):175-88. Am J Pathol. 1994. PMID: 7518193 Free PMC article.

3

Eosinophilia-myalgia syndrome: a clinicopathological study of four patients.

Villanova M, De Clerck LS, Cras P, Ceuterick C, Van Marck E, Guazzi GC, Martin JJ. Villanova M, et al. Clin Neuropathol. 1993 Jul-Aug;12(4):201-3. Clin Neuropathol. 1993. PMID: 8403629

4

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. J Submicrosc Cytol Pathol. 1996 Jan;28(1):1-4. J Submicrosc Cytol Pathol. 1996. PMID: 8929621

5

Detection of beta-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren).

Villanova M, Ceuterick C, Dotti MT, Santorelli FM, Casali C, Malandrini A, De Stefano N, Lübke U, Martin JJ, Guazzi GC, Federico A. Villanova M, et al. Acta Neuropathol. 1999 Jul;98(1):78-84. doi: 10.1007/s004010051053. Acta Neuropathol. 1999. PMID: 10412803

6

Eosinophilia myalgia syndrome: absence of immunoglobulin reactivity suggests a cellular rather than humoral mechanism.

Villanova M, De Clerck LS, Cras P, Guazzi GC, Martin JJ. Villanova M, et al. Acta Neurol Belg. 1994;94(3):200-4. Acta Neurol Belg. 1994. PMID: 7976226

7

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. Neuromuscul Disord. 1996 May;6(3):167-72. doi: 10.1016/0960-8966(96)00016-8. Neuromuscul Disord. 1996. PMID: 8784804

8

Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study.

Malandrini A, Villanova M, Sabatelli P, Squarzoni S, Six J, Toti P, Guazzi G, Maraldi NM. Malandrini A, et al. Among authors: villanova m. Acta Neuropathol. 1997 Feb;93(2):166-72. doi: 10.1007/s004010050598. Acta Neuropathol. 1997. PMID: 9039464

9

Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study.

Villanova M, Malandrini A, Sabatelli P, Sewry CA, Toti P, Torelli S, Six J, Scarfó G, Palma L, Muntoni F, Squarzoni S, Tosi P, Maraldi NM, Guazzi GC. Villanova M, et al. Acta Neuropathol. 1997 Dec;94(6):567-71. doi: 10.1007/s004010050751. Acta Neuropathol. 1997. PMID: 9444358

10

Inflammatory pathogenesis of cortical polymicrogyria: an autopsy study.

Toti P, De Felice C, Palmeri ML, Villanova M, Martín JJ, Buonocore G. Toti P, et al. Among authors: villanova m. Pediatr Res. 1998 Sep;44(3):291-6. doi: 10.1203/00006450-199809000-00005. Pediatr Res. 1998. PMID: 9727703

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