Servidei S - Search Results

1

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

Ciafaloni E, Ricci E, Servidei S, Shanske S, Silvestri G, Manfredi G, Schon EA, DiMauro S. Ciafaloni E, et al. Among authors: servidei s. Neurology. 1991 Oct;41(10):1663-4. doi: 10.1212/wnl.41.10.1663. Neurology. 1991. PMID: 1922812 No abstract available.

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

Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach.

Tritschler HJ, Bonilla E, Lombes A, Andreetta F, Servidei S, Schneyder B, Miranda AF, Schon EA, Kadenbach B, DiMauro S. Tritschler HJ, et al. Among authors: servidei s. Neurology. 1991 Feb;41(2 ( Pt 1)):300-5. doi: 10.1212/wnl.41.2_part_1.300. Neurology. 1991. PMID: 1846953

5

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

6

Metabolic causes of myoglobinuria.

Tonin P, Lewis P, Servidei S, DiMauro S. Tonin P, et al. Among authors: servidei s. Ann Neurol. 1990 Feb;27(2):181-5. doi: 10.1002/ana.410270214. Ann Neurol. 1990. PMID: 2156480

7

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

Zeviani M, Gellera C, Pannacci M, Uziel G, Prelle A, Servidei S, DiDonato S. Zeviani M, et al. Among authors: servidei s. Ann Neurol. 1990 Jul;28(1):94-7. doi: 10.1002/ana.410280118. Ann Neurol. 1990. PMID: 2375642

8

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S, et al. Moraes CT, et al. Among authors: servidei s. N Engl J Med. 1989 May 18;320(20):1293-9. doi: 10.1056/NEJM198905183202001. N Engl J Med. 1989. PMID: 2541333

9

Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.

Haller RG, Lewis SF, Estabrook RW, DiMauro S, Servidei S, Foster DW. Haller RG, et al. Among authors: servidei s. J Clin Invest. 1989 Jul;84(1):155-61. doi: 10.1172/JCI114135. J Clin Invest. 1989. PMID: 2544623 Free PMC article.

10

Disorders of glycogen metabolism of muscle.

Servidei S, DiMauro S. Servidei S, et al. Neurol Clin. 1989 Feb;7(1):159-78. Neurol Clin. 1989. PMID: 2646520 Review.

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