Casali C - Search Results

1

The emerging concept of mitochondrial cardiomyopathies.

Santorelli FM, Tessa A, D'amati G, Casali C. Santorelli FM, et al. Among authors: casali c. Am Heart J. 2001 Jan;141(1):E1. doi: 10.1067/mhj.2001.112088. Am Heart J. 2001. PMID: 11136504 Review.

2

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.

3

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

4

Detection of deleted mitochondrial DNA in Kearns-Sayre syndrome using laser capture microdissection.

Pistilli D, di Gioia CR, D'Amati G, Sciacchitano S, Quaglione R, Quitadamo R, Casali C, Gallo P, Santorelli FM. Pistilli D, et al. Among authors: casali c. Hum Pathol. 2003 Oct;34(10):1058-61. doi: 10.1053/s0046-8177(03)00344-7. Hum Pathol. 2003. PMID: 14608542

5

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM. Taylor RW, et al. Among authors: casali c. J Am Coll Cardiol. 2003 May 21;41(10):1786-96. doi: 10.1016/s0735-1097(03)00300-0. J Am Coll Cardiol. 2003. PMID: 12767666 Free article.

6

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.

7

[Mitochondrial diseases].

D'Amati G, Casali C, Giordano C. D'Amati G, et al. Among authors: casali c. Pathologica. 1999 Feb;91(1):49-50. Pathologica. 1999. PMID: 10396951 Review. Italian. No abstract available.

8

Chronic diarrhea associated with the A3243G mtDNA mutation.

Santorelli FM, Villanova M, Malandrini A, Grieco GS, Palmeri S, Merlini L, Casali C. Santorelli FM, et al. Among authors: casali c. Neurology. 2000 Jan 11;54(1):266-7. doi: 10.1212/wnl.54.1.266. Neurology. 2000. PMID: 10636171 No abstract available.

9

Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndrome.

De Joanna G, Santorelli FM, Casali C, Brescia-Morra V, Perretti A, Santoro L. De Joanna G, et al. Among authors: casali c. J Hum Genet. 2000;45(2):109-11. doi: 10.1007/s100380050025. J Hum Genet. 2000. PMID: 10721677

10

Multiple mtDNA deletions: clinical and molecular correlations.

Santorelli FM, De Joanna G, Casali C, Tessa A, Siciliano G, Amabile GA, Pierelli F, Vilarinho L, Santoro L. Santorelli FM, et al. Among authors: casali c. J Inherit Metab Dis. 2000 Mar;23(2):155-61. doi: 10.1023/a:1005617916260. J Inherit Metab Dis. 2000. PMID: 10801057

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