Casali C - Search Results

1

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.

2

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

3

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.

4

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.

5

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

6

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.

7

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation.

Santorelli FM, Tanji K, Manta P, Casali C, Krishna S, Hays AP, Mancini DM, DiMauro S, Hirano M. Santorelli FM, et al. Among authors: casali c. Am J Hum Genet. 1999 Jan;64(1):295-300. doi: 10.1086/302188. Am J Hum Genet. 1999. PMID: 9915970 Free PMC article. No abstract available.

8

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.

9

Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid.

Casali C, d'Amati G, Bernucci P, DeBiase L, Autore C, Santorelli FM, Coviello D, Gallo P. Casali C, et al. J Am Coll Cardiol. 1999 May;33(6):1584-9. doi: 10.1016/s0735-1097(99)00079-0. J Am Coll Cardiol. 1999. PMID: 10334428 Free article.

10

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. Among authors: casali c. Acta Neuropathol. 1999 Jul;98(1):78-84. doi: 10.1007/s004010051053. Acta Neuropathol. 1999. PMID: 10412803

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