Casali C - Search Results

1

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.

Casali C, Valente EM, Bertini E, Montagna G, Criscuolo C, De Michele G, Villanova M, Damiano M, Pierallini A, Brancati F, Scarano V, Tessa A, Cricchi F, Grieco GS, Muglia M, Carella M, Martini B, Rossi A, Amabile GA, Nappi G, Filla A, Dallapiccola B, Santorelli FM. Casali C, et al. Neurology. 2004 Jan 27;62(2):262-8. doi: 10.1212/wnl.62.2.262. Neurology. 2004. PMID: 14745065

2

Pilomotor epilepsy.

Scoppetta C, Casali C, D'Agostini S, Amabile G, Morocutti C. Scoppetta C, et al. Among authors: casali c. Funct Neurol. 1989 Jul-Sep;4(3):283-6. Funct Neurol. 1989. PMID: 2676747 Review.

3

[Inflammatory myopathies].

Scoppetta C, Casali C, D'Agostini S, Pauri F, Amabile G. Scoppetta C, et al. Among authors: casali c. Riv Neurol. 1988 Jan-Feb;58(1):11-4. Riv Neurol. 1988. PMID: 3420371 Italian. No abstract available.

4

A novel mtDNA point mutation in maternally inherited cardiomyopathy.

Casali C, Santorelli FM, D'Amati G, Bernucci P, DeBiase L, DiMauro S. Casali C, et al. Biochem Biophys Res Commun. 1995 Aug 15;213(2):588-93. doi: 10.1006/bbrc.1995.2172. Biochem Biophys Res Commun. 1995. PMID: 7646516

5

Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A).

Santorelli FM, Mak SC, El-Schahawi M, Casali C, Shanske S, Baram TZ, Madrid RE, DiMauro S. Santorelli FM, et al. Among authors: casali c. Am J Hum Genet. 1996 May;58(5):933-9. Am J Hum Genet. 1996. PMID: 8651277 Free PMC article.

6

Mitochondrial tRNA(Cys) gene mutation (A5814G): a second family with mitochondrial encephalopathy.

Santorelli FM, Siciliano G, Casali C, Basirico MG, Carrozzo R, Calvosa F, Sartucci F, Bonfiglio L, Murri L, DiMauro S. Santorelli FM, et al. Among authors: casali c. Neuromuscul Disord. 1997 May;7(3):156-9. doi: 10.1016/s0960-8966(97)00444-6. Neuromuscul Disord. 1997. PMID: 9185178 Free article.

7

Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses.

Carrozzo R, Hirano M, Fromenty B, Casali C, Santorelli FM, Bonilla E, DiMauro S, Schon EA, Miranda AF. Carrozzo R, et al. Among authors: casali c. Neurology. 1998 Jan;50(1):99-106. doi: 10.1212/wnl.50.1.99. Neurology. 1998. PMID: 9443465

8

Genetic heterogeneity of myoclonus epilepsy with ragged-red fibers syndrome.

Santorelli FM, Casali C. Santorelli FM, et al. Among authors: casali c. Muscle Nerve. 1998 May;21(5):681-2. doi: 10.1002/(sici)1097-4598(199805)21:5<681::aid-mus27>3.0.co;2-x. Muscle Nerve. 1998. PMID: 9572259 No abstract available.

9

Mitochondrial myopathy mimicking fibromyalgia syndrome.

Villanova M, Selvi E, Malandrini A, Casali C, Santorelli FM, De Stefano R, Marcolongo R. Villanova M, et al. Among authors: casali c. Muscle Nerve. 1999 Feb;22(2):289-91. doi: 10.1002/(sici)1097-4598(199902)22:2<289::aid-mus26>3.0.co;2-o. Muscle Nerve. 1999. PMID: 10024147 No abstract available.

10

Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family.

Casali C, Fabrizi GM, Santorelli FM, Colazza G, Villanova M, Dotti MT, Cavallaro T, Cardaioli E, Battisti C, Manneschi L, DiGennaro GC, Fortini D, Spadaro M, Morocutti C, Federico A. Casali C, et al. Neurology. 1999 Mar 23;52(5):1103-4. doi: 10.1212/wnl.52.5.1103. Neurology. 1999. PMID: 10102446 No abstract available.

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