Dotti MT - Search Results

1

NGS in Hereditary Ataxia: When Rare Becomes Frequent.

Galatolo D, De Michele G, Silvestri G, Leuzzi V, Casali C, Musumeci O, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Caputi C, Cioffi E, De Michele G, Dotti MT, Fico T, Fiorillo C, Galosi S, Lieto M, Malandrini A, Melone MAB, Mignarri A, Natale G, Pegoraro E, Petrucci A, Ricca I, Riso V, Rossi S, Rubegni A, Scarlatti A, Tinelli F, Trovato R, Tedeschi G, Tessa A, Filla A, Santorelli FM. Galatolo D, et al. Among authors: dotti mt. Int J Mol Sci. 2021 Aug 6;22(16):8490. doi: 10.3390/ijms22168490. Int J Mol Sci. 2021. PMID: 34445196 Free PMC article.

2

Association of myopathy with multiple exostoses and mental retardation: a case report.

De Stefano N, Dotti MT, Malandrini A, Federico A. De Stefano N, et al. Among authors: dotti mt. Brain Dev. 1994 Mar-Apr;16(2):136-8. doi: 10.1016/0387-7604(94)90050-7. Brain Dev. 1994. PMID: 8048702

3

Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression.

Dotti MT, Malandrini A, Bartolini S, Fabrizi GM, Federico A. Dotti MT, et al. Brain Dev. 1993 Jul-Aug;15(4):291-4. doi: 10.1016/0387-7604(93)90026-5. Brain Dev. 1993. PMID: 8250152

4

Sensory-motor hereditary neuropathy with early onset. A case report.

Malandrini A, De Stefano N, Dotti MT, Vecchione V, Federico A. Malandrini A, et al. Among authors: dotti mt. Acta Neurol (Napoli). 1993 Apr;15(2):81-6. Acta Neurol (Napoli). 1993. PMID: 8328327

5

Optic atrophy in Marinesco-Sjögren syndrome: an additional ocular feature. Report of three cases in two families.

Dotti MT, Bardelli AM, De Stefano N, Federico A, Malandrini A, Vanni M, Guazzi GC. Dotti MT, et al. Ophthalmic Paediatr Genet. 1993 Mar;14(1):5-7. doi: 10.3109/13816819309087616. Ophthalmic Paediatr Genet. 1993. PMID: 8345957

6

Plasma levels of vitamin E in Parkinson's disease.

Federico A, Battisti C, Formichi P, Dotti MT. Federico A, et al. Among authors: dotti mt. J Neural Transm Suppl. 1995;45:267-70. J Neural Transm Suppl. 1995. PMID: 8748634

7

Disappearance of skin lipofuscin storage and marked clinical improvement in adult onset coeliac disease and severe vitamin E deficiency after chronic vitamin E megatherapy.

Battisti C, Dotti MT, Formichi P, Bonuccelli U, Malandrini A, Carrai M, Tripodi SA, Federico A. Battisti C, et al. Among authors: dotti mt. J Submicrosc Cytol Pathol. 1996 Jul;28(3):339-44. J Submicrosc Cytol Pathol. 1996. PMID: 8765578

8

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: dotti mt. J Neurol Sci. 1997 Aug;149(2):147-50. doi: 10.1016/s0022-510x(97)05381-1. J Neurol Sci. 1997. PMID: 9171322

9

Selective ipsilateral neuromuscular involvement in a case of facial and somatic hemiatrophy.

Malandrini A, Dotti MT, Federico A. Malandrini A, et al. Among authors: dotti mt. Muscle Nerve. 1997 Jul;20(7):890-2. doi: 10.1002/(sici)1097-4598(199707)20:7<890::aid-mus16>3.0.co;2-w. Muscle Nerve. 1997. PMID: 9179164 No abstract available.

10

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: dotti mt. J Submicrosc Cytol Pathol. 1997 Jul;29(3):335-8. J Submicrosc Cytol Pathol. 1997. PMID: 9267042

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