Malandrini A - Search Results

1

Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL.

Malandrini A, Albani F, Palmeri S, Fattapposta F, Gambelli S, Berti G, Bracco A, Tammaro A, Calzavara S, Villanova M, Ferrari M, Rossi A, Carrera P. Malandrini A, et al. Neurology. 2002 Aug 27;59(4):617-20. doi: 10.1212/wnl.59.4.617. Neurology. 2002. PMID: 12196662

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

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

4

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.

5

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

6

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

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

Amiodarone induced lipidosis similar to Niemann-Pick C disease. Biochemical and morphological study.

Palmeri S, Battisti C, Malandrini A, Federico A. Palmeri S, et al. Among authors: malandrini a. Life Sci. 1995;57(21):1963-71. doi: 10.1016/0024-3205(95)02129-7. Life Sci. 1995. PMID: 7475945

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

228 results

Search Page

Filters