Casali C - Search Results

1

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.

Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM. Grieco GS, et al. Among authors: casali c. Neurology. 2004 Jan 13;62(1):103-6. doi: 10.1212/01.wnl.0000104491.66816.77. Neurology. 2004. PMID: 14718707

2

Infantile autosomal dominant distal myopathy.

Scoppetta C, Casali C, La Cesa I, Sermoni A, Mercuri B, Pierelli F, Vaccario ML. Scoppetta C, et al. Among authors: casali c. Acta Neurol Scand. 1995 Aug;92(2):122-6. doi: 10.1111/j.1600-0404.1995.tb01024.x. Acta Neurol Scand. 1995. PMID: 7484058 Review.

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

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

5

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.

6

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.

7

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.

8

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.

9

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

10

MtDNA-related idiopathic dilated cardiomyopathy.

Tessa A, Vilarinho L, Casali C, Santorelli FM. Tessa A, et al. Among authors: casali c. Eur J Hum Genet. 1999 Dec;7(8):847-8. doi: 10.1038/sj.ejhg.5200380. Eur J Hum Genet. 1999. PMID: 10602359 No abstract available.

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