Malandrini A - Search Results

1

Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 cases.

Malandrini A, Selvi E, Villanova M, Berti G, Sabadini L, Salvadori C, Gambelli S, De Stefano R, Vernillo R, Marcolongo R, Guazzi G. Malandrini A, et al. J Rheumatol. 2000 May;27(5):1203-6. J Rheumatol. 2000. PMID: 10813288

2

Sensory-motor chronic neuropathy in two siblings: atypical presentation of tomaculous neuropathy.

Malandrini A, Guazzi GC, Federico A. Malandrini A, et al. Clin Neuropathol. 1992 Nov-Dec;11(6):318-22. Clin Neuropathol. 1992. PMID: 1473315

3

The clinical aspects of adult hexosaminidase deficiencies.

Federico A, Palmeri S, Malandrini A, Fabrizi G, Mondelli M, Guazzi GC. Federico A, et al. Among authors: malandrini a. Dev Neurosci. 1991;13(4-5):280-7. doi: 10.1159/000112174. Dev Neurosci. 1991. PMID: 1840098 Review.

4

Giant axonal neuropathy in 2 siblings: a generalized disorder of intermediate filaments.

Guazzi GC, Malandrini A, Gerli R, Federico A. Guazzi GC, et al. Among authors: malandrini a. Eur Neurol. 1991;31(1):50-6. doi: 10.1159/000116646. Eur Neurol. 1991. PMID: 2015839

5

Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy.

Federico A, Dotti MT, Fabrizi GM, Palmeri S, Massimo L, Robinson BH, Malandrini A, Guazzi GC. Federico A, et al. Among authors: malandrini a. Eur Neurol. 1990;30(3):123-7. doi: 10.1159/000117327. Eur Neurol. 1990. PMID: 2162773

6

Peripheral nerve involvement in ataxia telangiectasia: histological and ultrastructural studies of peroneal nerve biopsy in two cases.

Malandrini A, Guazzi GC, Alessandrini C, Federico A. Malandrini A, et al. Clin Neuropathol. 1990 May-Jun;9(3):109-14. Clin Neuropathol. 1990. PMID: 2163784

7

Infanto-juvenile encephaloneuropathy and pigmentary retinopathy in a girl associated with congenital adrenal insufficiency and altered plasma medium-chain fatty acid levels.

Federico A, Baracchini G, Dotti MT, Ibba L, Malandrini A, Ciacci G, Meloni M, Palmeri S, Pompella A, Guazzi GC. Federico A, et al. Among authors: malandrini a. J Inherit Metab Dis. 1988;11 Suppl 2:178-82. doi: 10.1007/BF01804229. J Inherit Metab Dis. 1988. PMID: 2846958 No abstract available.

8

Adrenomyeloneurodystrophy with late cerebral involvement and evidence of a multiple autoimmune disorder.

Federico A, Dotti MT, Annunziata P, Bonuccelli U, Fenzi G, Ciacci G, Malandrini A, Meucci G, Guazzi GC. Federico A, et al. Among authors: malandrini a. J Inherit Metab Dis. 1988;11 Suppl 2:169-72. doi: 10.1007/BF01804227. J Inherit Metab Dis. 1988. PMID: 3141701 No abstract available.

9

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. Brain Dev. 1995 Jul-Aug;17(4):286-90. doi: 10.1016/0387-7604(95)00039-e. Brain Dev. 1995. PMID: 7503394

10

Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family.

Malandrini A, Fabrizi GM, Truschi F, Di Pietro G, Moschini F, Bartalucci P, Berti G, Salvadori C, Bucalossi A, Guazzi G. Malandrini A, et al. J Neurol Sci. 1994 Jun;124(1):89-94. doi: 10.1016/0022-510x(94)90016-7. J Neurol Sci. 1994. PMID: 7931427

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