Carrozzo R - Search Results

1

Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitine.

Brevetti G, Fanin M, De Amicis V, Carrozzo R, Di Lello F, Martone VD, Angelini C. Brevetti G, et al. Among authors: carrozzo r. Muscle Nerve. 1997 Sep;20(9):1115-20. doi: 10.1002/(sici)1097-4598(199709)20:9<1115::aid-mus4>3.0.co;2-b. Muscle Nerve. 1997. PMID: 9270666 Clinical Trial.

2

Muscle carnitine deficiency in patients with severe peripheral vascular disease.

Brevetti G, Angelini C, Rosa M, Carrozzo R, Perna S, Corsi M, Matarazzo A, Marcialis A. Brevetti G, et al. Among authors: carrozzo r. Circulation. 1991 Oct;84(4):1490-5. doi: 10.1161/01.cir.84.4.1490. Circulation. 1991. PMID: 1914091

3

Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.

Martinuzzi A, Vergani L, Carrozzo R, Fanin M, Bartoloni L, Angelini C, Askanas V, Engel WK. Martinuzzi A, et al. Among authors: carrozzo r. J Clin Invest. 1993 Oct;92(4):1774-80. doi: 10.1172/JCI116766. J Clin Invest. 1993. PMID: 8408630 Free PMC article.

4

Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect.

Angelini C, Melacini P, Valente ML, Reichmann H, Carrozzo R, Fanin M, Vergani L, Boffa GM, Martinuzzi A, Fasoli G. Angelini C, et al. Among authors: carrozzo r. Jpn Heart J. 1993 Jan;34(1):63-77. doi: 10.1536/ihj.34.63. Jpn Heart J. 1993. PMID: 8515573

5

Liver fatty acid-binding protein in two cases of human lipid storage.

Vergani L, Fanin M, Martinuzzi A, Galassi A, Appi A, Carrozzo R, Rosa M, Angelini C. Vergani L, et al. Among authors: carrozzo r. Mol Cell Biochem. 1990 Oct 15-Nov 8;98(1-2):225-30. doi: 10.1007/BF00231388. Mol Cell Biochem. 1990. PMID: 2266963

6

Variability of the expression of muscle mitochondrial damage in ocular mitochondrial myopathy.

Siciliano G, Rossi B, Angelini C, Martinuzzi A, Carrozzo R, Bevilacqua G, Viacava P, Federico A, Fabrizi GM, Muratorio A. Siciliano G, et al. Among authors: carrozzo r. Neuromuscul Disord. 1992;2(5-6):397-404. doi: 10.1016/s0960-8966(06)80011-8. Neuromuscul Disord. 1992. PMID: 1300188

7

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

Vergani L, Martinuzzi A, Carelli V, Cortelli P, Montagna P, Schievano G, Carrozzo R, Angelini C, Lugaresi E. Vergani L, et al. Among authors: carrozzo r. Biochem Biophys Res Commun. 1995 May 25;210(3):880-8. doi: 10.1006/bbrc.1995.1740. Biochem Biophys Res Commun. 1995. PMID: 7763260

8

Correlation between clinical and molecular features in two MELAS families.

Martinuzzi A, Bartolomei L, Carrozzo R, Mostacciuolo M, Carbonin C, Toso V, Ciafaloni E, Shanske S, DiMauro S, Angelini C. Martinuzzi A, et al. Among authors: carrozzo r. J Neurol Sci. 1992 Dec;113(2):222-9. doi: 10.1016/0022-510x(92)90250-o. J Neurol Sci. 1992. PMID: 1487758

9

A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency.

Santoro L, Carrozzo R, Malandrini A, Piemonte F, Patrono C, Villanova M, Tessa A, Palmeri S, Bertini E, Santorelli FM. Santoro L, et al. Among authors: carrozzo r. Neuromuscul Disord. 2000 Aug;10(6):450-3. doi: 10.1016/s0960-8966(99)00122-4. Neuromuscul Disord. 2000. PMID: 10899453

10

Deficient muscle carnitine transport in primary carnitine deficiency.

Pons R, Carrozzo R, Tein I, Walker WF, Addonizio LJ, Rhead W, Miranda AF, Dimauro S, De Vivo DC. Pons R, et al. Among authors: carrozzo r. Pediatr Res. 1997 Nov;42(5):583-7. doi: 10.1203/00006450-199711000-00005. Pediatr Res. 1997. PMID: 9357927

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