Manneschi L - Search Results

1

A rare association of myasthenia gravis and mitochondrial myopathy: a clinical, biochemical and morphologic study of one case.

Plewnia K, Dotti MT, Malandrini A, Manneschi L, Battisti C, De Stefano N, Rufa A, Motolese E, Federico A. Plewnia K, et al. Among authors: manneschi l. J Submicrosc Cytol Pathol. 1997 Jul;29(3):335-8. J Submicrosc Cytol Pathol. 1997. PMID: 9267042

2

Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study.

Dotti MT, Manneschi L, Malandrini A, De Stefano N, Caznerale F, Federico A. Dotti MT, et al. Among authors: manneschi l. Brain Dev. 1993 Mar-Apr;15(2):103-6. doi: 10.1016/0387-7604(93)90045-a. Brain Dev. 1993. PMID: 8214327

3

Palpebral ptosis and muscle fatiguability associated with perineurial cell ensheathment of muscle fibers: a new disease of the neuromuscular junction?

Federico A, Plewnia K, Battisti C, Cavallaro T, Dotti MT, Malandrini A, Manneschi L. Federico A, et al. Among authors: manneschi l. J Neurol Sci. 1997 Aug;149(2):147-50. doi: 10.1016/s0022-510x(97)05381-1. J Neurol Sci. 1997. PMID: 9171322

4

Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study.

Federico A, Dotti MT, Cardaioli E, Grieco G, Malandrini A, Manneschi L, Plewnia K, Rufa A, Renieri A, Bruttini M, Perticoni GF. Federico A, et al. Among authors: manneschi l. J Submicrosc Cytol Pathol. 1998 Oct;30(4):521-6. J Submicrosc Cytol Pathol. 1998. PMID: 9851061

5

Histochemical, ultrastructural and biochemical study of muscle mitochondria in Leber's hereditary optic atrophy.

Federico A, Manneschi L, Meloni M, Alessandrini C, Bardelli AM, Dotti MT, Sabatelli P. Federico A, et al. Among authors: manneschi l. J Inherit Metab Dis. 1988;11 Suppl 2:193-7. doi: 10.1007/BF01804233. J Inherit Metab Dis. 1988. PMID: 2846962 No abstract available.

6

Morphometric and biochemical study of muscle mitochondria in adult chronic progressive external ophthalmoplegia.

Federico A, Manneschi L, Sabatelli P, Dotti MT, Ciacci G, Ibba L, Gerli R. Federico A, et al. Among authors: manneschi l. J Inherit Metab Dis. 1988;11 Suppl 2:198-201. doi: 10.1007/BF01804234. J Inherit Metab Dis. 1988. PMID: 2846963 No abstract available.

7

Mitochondrial enzyme deficiency in cerebrotendinous xanthomatosis.

Dotti MT, Manneschi L, Federico A. Dotti MT, et al. Among authors: manneschi l. J Neurol Sci. 1995 Apr;129(2):106-8. doi: 10.1016/0022-510x(94)00256-n. J Neurol Sci. 1995. PMID: 7608723

8

Polarographic analyses of subsarcolemmal and intermyofibrillar mitochondria from rat skeletal and cardiac muscle.

Manneschi L, Federico A. Manneschi L, et al. J Neurol Sci. 1995 Feb;128(2):151-6. doi: 10.1016/0022-510x(94)00227-f. J Neurol Sci. 1995. PMID: 7738591

9

The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.

Fabrizi GM, Cardaioli E, Grieco GS, Cavallaro T, Malandrini A, Manneschi L, Dotti MT, Federico A, Guazzi G. Fabrizi GM, et al. Among authors: manneschi l. J Neurol Neurosurg Psychiatry. 1996 Jul;61(1):47-51. doi: 10.1136/jnnp.61.1.47. J Neurol Neurosurg Psychiatry. 1996. PMID: 8676159 Free PMC article.

10

Amiodarone affects membrane water permeability properties of human erythrocytes and rat mitochondria.

Federico A, Battisti C, Manneschi L, Gaggelli E, Tassini M, Valensin G, Vivi A. Federico A, et al. Among authors: manneschi l. Eur J Pharmacol. 1996 May 23;304(1-3):237-41. doi: 10.1016/0014-2999(96)00148-3. Eur J Pharmacol. 1996. PMID: 8813607

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