Malandrini A - Search Results

1

A second MNGIE patient without typical mitochondrial skeletal muscle involvement.

Cardaioli E, Da Pozzo P, Malfatti E, Battisti C, Gallus GN, Gaudiano C, Macucci M, Malandrini A, Margollicci M, Rubegni A, Dotti MT, Federico A. Cardaioli E, et al. Among authors: malandrini a. Neurol Sci. 2010 Aug;31(4):491-4. doi: 10.1007/s10072-010-0225-5. Epub 2010 Mar 16. Neurol Sci. 2010. PMID: 20232099

2

Dementia, myoclonus, peripheral neuropathy, and lipid-like material in skin biopsy during psychotropic drug treatment.

Federico A, Palmeri S, Malandrini A, Mangano L, Ciacci G, Scarpini C, Tiacci G. Federico A, et al. Among authors: malandrini a. Biol Psychiatry. 1992 Oct 15;32(8):721-7. doi: 10.1016/0006-3223(92)90303-h. Biol Psychiatry. 1992. PMID: 1333826

3

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

4

Imipramine induced lipidosis and dexamethasone effect: morphological and biochemical study in normal and chronic GM2 gangliosidosis fibroblasts.

Palmeri S, Mangano L, Battisti C, Malandrini A, Federico A. Palmeri S, et al. Among authors: malandrini a. J Neurol Sci. 1992 Jul;110(1-2):215-21. doi: 10.1016/0022-510x(92)90030-o. J Neurol Sci. 1992. PMID: 1506862

5

Vitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case report.

Federico A, Battisti C, Eusebi MP, de Stefano N, Malandrini A, Mondelli M, Volpi N. Federico A, et al. Among authors: malandrini a. Eur Neurol. 1991;31(6):366-71. doi: 10.1159/000116695. Eur Neurol. 1991. PMID: 1661677

6

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.

7

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

8

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

9

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

10

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.

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