Parrotta E - Search Results

1

Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions.

Malandrini A, Scarpini C, Villanova M, Sicurelli F, Parrotta E, DeFalco D, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. Acta Neurol Scand. 1996 Jul;94(1):60-2. doi: 10.1111/j.1600-0404.1996.tb00040.x. Acta Neurol Scand. 1996. PMID: 8874595

2

Myopathic involvement in two cases of Hallervorden-Spatz disease.

Malandrini A, Bonuccelli U, Parrotta E, Ceravolo R, Berti G, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. Brain Dev. 1995 Jul-Aug;17(4):286-90. doi: 10.1016/0387-7604(95)00039-e. Brain Dev. 1995. PMID: 7503394

3

Mitochondrial changes in steroid myopathy with respiratory failure and rapid fatal course: report of a case.

Malandrini A, Scarpini C, Fabrizi GM, Manneschi L, Rosi R, Parrotta E, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. Eur Neurol. 1995;35(3):182-3. doi: 10.1159/000117123. Eur Neurol. 1995. PMID: 7628504 No abstract available.

4

Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter.

Malandrini A, Scarpini C, Fabrizi GM, Parrotta E, Salvadori C, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. J Neurol Sci. 1995 Oct;132(2):195-200. doi: 10.1016/0022-510x(95)00156-v. J Neurol Sci. 1995. PMID: 8543948

5

Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency.

Villanova M, Malandrini A, Biancotti R, Löfgren A, Mongini T, Six J, Salvestroni R, Parrotta E, Van Broeckhoven C, Paolozzi C, Guazzi G. Villanova M, et al. Among authors: parrotta e. Neuromuscul Disord. 1996 May;6(3):167-72. doi: 10.1016/0960-8966(96)00016-8. Neuromuscul Disord. 1996. PMID: 8784804

6

Neuronal intranuclear inclusion disease: polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case.

Malandrini A, Fabrizi GM, Cavallaro T, Zazzi M, Parrotta E, Romano L, Berti G, Villanova M, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. Acta Neuropathol. 1996;91(2):215-8. doi: 10.1007/s004010050417. Acta Neuropathol. 1996. PMID: 8787158

7

Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities.

Malandrini A, Cesaretti S, Mulinari M, Palmeri S, Fabrizi GM, Villanova M, Parrotta E, Montagnani A, Montagnani M, Anichini M, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. J Neurol Sci. 1996 Sep 1;140(1-2):129-31. doi: 10.1016/0022-510x(96)00155-4. J Neurol Sci. 1996. PMID: 8866438

8

Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy.

Malandrini A, Scarpini C, Palmeri S, Villanova M, Parrotta E, Tripodi S, Giani S, DeFalco D, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. Brain Dev. 1996 Jan-Feb;18(1):59-63. doi: 10.1016/0387-7604(95)00098-4. Brain Dev. 1996. PMID: 8907345

9

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers.

Malandrini A, Palmeri S, Villanova M, Parrotta E, Sicurelli F, Amato D, DeFalco D, Guazzi GC. Malandrini A, et al. Among authors: parrotta e. Brain Dev. 1997 Apr;19(3):209-11. doi: 10.1016/s0387-7604(96)00563-3. Brain Dev. 1997. PMID: 9134193

10

CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic study.

Malandrini A, Galli L, Villanova M, Palmeri S, Parrotta E, DeFalco D, Cappelli M, Grieco GS, Renieri A, Guazzi G. Malandrini A, et al. Among authors: parrotta e. Eur Neurol. 1998 Oct;40(3):164-8. doi: 10.1159/000007974. Eur Neurol. 1998. PMID: 9748675

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