Servidei S - Search Results

1

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.

Ricci E, Galluzzi G, Deidda G, Cacurri S, Colantoni L, Merico B, Piazzo N, Servidei S, Vigneti E, Pasceri V, Silvestri G, Mirabella M, Mangiola F, Tonali P, Felicetti L. Ricci E, et al. Among authors: servidei s. Ann Neurol. 1999 Jun;45(6):751-7. doi: 10.1002/1531-8249(199906)45:6<751::aid-ana9>3.0.co;2-m. Ann Neurol. 1999. PMID: 10360767

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

Somatosensory and motor evoked potentials in the assessment of cerebrotendinous xanthomatosis before and after treatment with chenodeoxycholic acid: a preliminary study.

Restuccia D, Di Lazzaro V, Servidei S, Colosimo C, Tonali P. Restuccia D, et al. Among authors: servidei s. J Neurol Sci. 1992 Oct;112(1-2):139-46. doi: 10.1016/0022-510x(92)90143-9. J Neurol Sci. 1992. PMID: 1469424

5

Giant axonal neuropathy: report on a case with focal fiber loss.

Sabatelli M, Bertini E, Servidei S, Fernandez E, Magi S, Tonali P. Sabatelli M, et al. Among authors: servidei s. Acta Neuropathol. 1992;83(5):543-6. doi: 10.1007/BF00310034. Acta Neuropathol. 1992. PMID: 1621511

6

Benign monomelic amyotrophy of lower limb: report of three cases.

Uncini A, Servidei S, Delli Pizzi C, Cutarella R, Di Muzio A, Gambi D, Tonali P. Uncini A, et al. Among authors: servidei s. Acta Neurol Scand. 1992 Jun;85(6):397-400. doi: 10.1111/j.1600-0404.1992.tb06035.x. Acta Neurol Scand. 1992. PMID: 1642110

7

Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study.

Bertini E, Bosman C, Ricci E, Servidei S, Boldrini R, Sabatelli M, Salviati G. Bertini E, et al. Among authors: servidei s. Acta Neuropathol. 1991;81(6):632-40. doi: 10.1007/BF00296373. Acta Neuropathol. 1991. PMID: 1882639

8

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.

9

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

10

Involvement of respiratory muscles in cytoplasmic body myopathy--a pathology study.

Bertini E, Ricci E, Boldrini R, Servidei S, Fusilli S, Dionisi-Vici C, Bosman C, Bonilla E. Bertini E, et al. Among authors: servidei s. Brain Dev. 1990;12(6):798-806. doi: 10.1016/s0387-7604(12)80010-6. Brain Dev. 1990. PMID: 2092592

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