Antozzi C - Search Results

1

OXPHOS defects and mitochondrial DNA mutations in cardiomyopathy.

Zeviani M, Mariotti C, Antozzi C, Fratta GM, Rustin P, Prelle A. Zeviani M, et al. Among authors: antozzi c. Muscle Nerve Suppl. 1995;3:S170-4. doi: 10.1002/mus.880181433. Muscle Nerve Suppl. 1995. PMID: 7603520

2

Defects of mitochondrial DNA.

Zeviani M, Antozzi C. Zeviani M, et al. Among authors: antozzi c. Brain Pathol. 1992 Apr;2(2):121-32. doi: 10.1111/j.1750-3639.1992.tb00680.x. Brain Pathol. 1992. PMID: 1341953 Review.

3

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Zeviani M, Gellera C, Antozzi C, Rimoldi M, Morandi L, Villani F, Tiranti V, DiDonato S. Zeviani M, et al. Among authors: antozzi c. Lancet. 1991 Jul 20;338(8760):143-7. doi: 10.1016/0140-6736(91)90136-d. Lancet. 1991. PMID: 1677065

4

Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

Zeviani M, Amati P, Bresolin N, Antozzi C, Piccolo G, Toscano A, DiDonato S. Zeviani M, et al. Among authors: antozzi c. Am J Hum Genet. 1991 Feb;48(2):203-11. Am J Hum Genet. 1991. PMID: 1899320 Free PMC article.

5

Epilepsia partialis continua associated with NADH-coenzyme Q reductase deficiency.

Antozzi C, Franceschetti S, Filippini G, Barbiroli B, Savoiardo M, Fiacchino F, Rimoldi M, Lodi R, Zaniol P, Zeviani M. Antozzi C, et al. J Neurol Sci. 1995 Apr;129(2):152-61. doi: 10.1016/0022-510x(94)00267-r. J Neurol Sci. 1995. PMID: 7608730

6

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.

Mariotti C, Savarese N, Suomalainen A, Rimoldi M, Comi G, Prelle A, Antozzi C, Servidei S, Jarre L, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: antozzi c. J Neurol. 1995 May;242(5):304-12. doi: 10.1007/BF00878873. J Neurol. 1995. PMID: 7643139

7

Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases.

Franceschetti S, Antozzi C, Binelli S, Carrara F, Nardocci N, Zeviani M, Avanzini G. Franceschetti S, et al. Among authors: antozzi c. Acta Neurol Scand. 1993 Mar;87(3):219-23. doi: 10.1111/j.1600-0404.1993.tb04105.x. Acta Neurol Scand. 1993. PMID: 8386419

8

Mitochondrial disorders.

Zeviani M, Antozzi C. Zeviani M, et al. Among authors: antozzi c. Mol Hum Reprod. 1997 Feb;3(2):133-48. doi: 10.1093/molehr/3.2.133. Mol Hum Reprod. 1997. PMID: 9239718 Review.

9

Cardiomyopathies in disorders of oxidative metabolism.

Antozzi C, Zeviani M. Antozzi C, et al. Cardiovasc Res. 1997 Aug;35(2):184-99. doi: 10.1016/s0008-6363(97)00141-7. Cardiovasc Res. 1997. PMID: 9349380 Review.

10

Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families.

Mariotti C, Castellotti B, Pareyson D, Testa D, Eoli M, Antozzi C, Silani V, Marconi R, Tezzon F, Siciliano G, Marchini C, Gellera C, Donato SD. Mariotti C, et al. Among authors: antozzi c. Neuromuscul Disord. 2000 Aug;10(6):391-7. doi: 10.1016/s0960-8966(99)00132-7. Neuromuscul Disord. 2000. PMID: 10899444

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