Servidei S - Search Results

1

Apoptosis and ROS detoxification enzymes correlate with cytochrome c oxidase deficiency in mitochondrial encephalomyopathies.

Di Giovanni S, Mirabella M, Papacci M, Odoardi F, Silvestri G, Servidei S. Di Giovanni S, et al. Among authors: servidei s. Mol Cell Neurosci. 2001 Apr;17(4):696-705. doi: 10.1006/mcne.2001.0970. Mol Cell Neurosci. 2001. PMID: 11312605

2

Disorders associated with depletion of mitochondrial DNA.

Ricci E, Moraes CT, Servidei S, Tonali P, Bonilla E, DiMauro S. Ricci E, et al. Among authors: servidei s. Brain Pathol. 1992 Apr;2(2):141-7. doi: 10.1111/j.1750-3639.1992.tb00682.x. Brain Pathol. 1992. PMID: 1341955 Review.

3

Fatal infantile liver failure associated with mitochondrial DNA depletion.

Mazziotta MR, Ricci E, Bertini E, Dionisi Vici C, Servidei S, Burlina AB, Sabetta G, Bartuli A, Manfredi G, Silvestri G, et al. Mazziotta MR, et al. Among authors: servidei s. J Pediatr. 1992 Dec;121(6):896-901. doi: 10.1016/s0022-3476(05)80335-x. J Pediatr. 1992. PMID: 1447652 Free article.

4

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.

Servidei S, Zeviani M, Manfredi G, Ricci E, Silvestri G, Bertini E, Gellera C, Di Mauro S, Di Donato S, Tonali P. Servidei S, et al. Neurology. 1991 Jul;41(7):1053-9. doi: 10.1212/wnl.41.7.1053. Neurology. 1991. PMID: 2067633

5

Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine.

Uncini A, Lodi R, Di Muzio A, Silvestri G, Servidei S, Lugaresi A, Iotti S, Zaniol P, Barbiroli B. Uncini A, et al. Among authors: servidei s. J Neurol Sci. 1995 Apr;129(2):214-22. doi: 10.1016/0022-510x(94)00283-t. J Neurol Sci. 1995. PMID: 7608738

6

Myasthenia gravis during interferon alfa therapy.

Batocchi AP, Evoli A, Servidei S, Palmisani MT, Apollo F, Tonali P. Batocchi AP, et al. Among authors: servidei s. Neurology. 1995 Feb;45(2):382-3. doi: 10.1212/wnl.45.2.382. Neurology. 1995. PMID: 7854543

7

Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings.

Bertini E, Salviati G, Apollo F, Ricci E, Servidei S, Broccolini A, Papacci M, Tonali P. Bertini E, et al. Among authors: servidei s. Acta Neuropathol. 1994;87(1):106-12. doi: 10.1007/BF00386261. Acta Neuropathol. 1994. PMID: 8140891

8

Ophthalmoplegia, demyelinating neuropathy, leukoencephalopathy, myopathy, and gastrointestinal dysfunction with multiple deletions of mitochondrial DNA: a mitochondrial multisystem disorder in search of a name.

Uncini A, Servidei S, Silvestri G, Manfredi G, Sabatelli M, Di Muzio A, Ricci E, Mirabella M, Di Mauro S, Tonali P. Uncini A, et al. Among authors: servidei s. Muscle Nerve. 1994 Jun;17(6):667-74. doi: 10.1002/mus.880170616. Muscle Nerve. 1994. PMID: 8196710

9

Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophy.

Mirabella M, Servidei S, Manfredi G, Ricci E, Frustaci A, Bertini E, Rana M, Tonali P. Mirabella M, et al. Among authors: servidei s. Neurology. 1993 Nov;43(11):2342-5. doi: 10.1212/wnl.43.11.2342. Neurology. 1993. PMID: 8232953

10

Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family.

Manfredi G, Silvestri G, Servidei S, Ricci E, Mirabella M, Bertini E, Papacci M, Rana M, Tonali P. Manfredi G, et al. Among authors: servidei s. J Neurol Sci. 1993 Mar;115(1):91-4. doi: 10.1016/0022-510x(93)90071-6. J Neurol Sci. 1993. PMID: 8468596

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