Toscano A - Search Results

1

Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases.

Sansone VA, Panzeri M, Montanari M, Apolone G, Gandossini S, Rose MR, Politano L, Solimene C, Siciliano G, Volpi L, Angelini C, Palmieri A, Toscano A, Musumeci O, Mongini T, Vercelli L, Massa R, Panico MB, Grandi M, Meola G. Sansone VA, et al. Among authors: toscano a. Eur J Neurol. 2010 Sep;17(9):1178-1187. doi: 10.1111/j.1468-1331.2010.02992.x. Epub 2010 Mar 30. Eur J Neurol. 2010. PMID: 20374278

2

Prevalence survey of major neurological disorders in Sicily. Results of a pilot study.

Vita G, Morgante L, Grigoletto F, Santoro M, Toscano A, Coraci MA, Meneghini F, Venuto C, Fazio C, Troilo G, et al. Vita G, et al. Among authors: toscano a. J Neurol. 1989 Sep;236(6):315-8. doi: 10.1007/BF00314371. J Neurol. 1989. PMID: 2795097

3

Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopy.

Vita G, Toscano A, Bresolin N, Meola G, Fortunato F, Baradello A, Barbiroli B, Frassineti C, Zaniol P, Messina C. Vita G, et al. Among authors: toscano a. J Neurol. 1994 Mar;241(5):289-94. doi: 10.1007/BF00868435. J Neurol. 1994. PMID: 8006681

4

Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism.

Vita G, Toscano A, Mileto G, Pitrone F, Ferrò MT, Gagliardi E, Bresolin N, Fortunato F, Messina C. Vita G, et al. Among authors: toscano a. Eur Neurol. 1993;33(2):168-72. doi: 10.1159/000116927. Eur Neurol. 1993. PMID: 8467827

5

Apoptosis in metabolic myopathies.

Monici MC, Toscano A, Girlanda P, Aguennouz M, Musumeci O, Vita G. Monici MC, et al. Among authors: toscano a. Neuroreport. 1998 Jul 13;9(10):2431-5. doi: 10.1097/00001756-199807130-00050. Neuroreport. 1998. PMID: 9694240

6

Phenotype modulators in myophosphorylase deficiency.

Martinuzzi A, Sartori E, Fanin M, Nascimbeni A, Valente L, Angelini C, Siciliano G, Mongini T, Tonin P, Tomelleri G, Toscano A, Merlini L, Bindoff LA, Bertelli S. Martinuzzi A, et al. Among authors: toscano a. Ann Neurol. 2003 Apr;53(4):497-502. doi: 10.1002/ana.10499. Ann Neurol. 2003. PMID: 12666117

7

Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL.

Lucchiari S, Pagliarani S, Salani S, Filocamo M, Di Rocco M, Melis D, Rodolico C, Musumeci O, Toscano A, Bresolin N, Comi GP. Lucchiari S, et al. Among authors: toscano a. Hum Mutat. 2006 Jun;27(6):600-1. doi: 10.1002/humu.9426. Hum Mutat. 2006. PMID: 16705713

8

Amyloid myopathy presenting with rhabdomyolysis: evidence of complement activation.

Rodolico C, Mazzeo A, Toscano A, Pastura C, Maimone D, Musumeci O, Musolino C, Vita G. Rodolico C, et al. Among authors: toscano a. Neuromuscul Disord. 2006 Aug;16(8):514-7. doi: 10.1016/j.nmd.2006.06.004. Epub 2006 Aug 21. Neuromuscul Disord. 2006. PMID: 16919949

9

Tarui disease and distal glycogenoses: clinical and genetic update.

Toscano A, Musumeci O. Toscano A, et al. Acta Myol. 2007 Oct;26(2):105-7. Acta Myol. 2007. PMID: 18421897 Free PMC article. Review.

10

POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study.

Messina S, Mora M, Pegoraro E, Pini A, Mongini T, D'Amico A, Pane M, Aiello C, Bruno C, Biancheri R, Berardinelli A, Boito C, Farina L, Morandi L, Moroni I, Pezzani R, Pichiecchio A, Ricci E, Ruggieri A, Saredi S, Scuderi C, Tessa A, Toscano A, Tortorella G, Trevisan CP, Uggetti C, Santorelli FM, Bertini E, Mercuri E. Messina S, et al. Among authors: toscano a. Neuromuscul Disord. 2008 Jul;18(7):565-71. doi: 10.1016/j.nmd.2008.04.004. Epub 2008 Jun 2. Neuromuscul Disord. 2008. PMID: 18513969

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