Mondelli M - Search Results

1

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: mondelli m. Dev Neurosci. 1991;13(4-5):280-7. doi: 10.1159/000112174. Dev Neurosci. 1991. PMID: 1840098 Review.

2

Neurophysiological study in chronic GM2 gangliosidosis (hexosaminidase A and B deficiency), with motor neuron disease phenotype.

Mondelli M, Rossi A, Palmeri S, Rizzuto N, Federico A. Mondelli M, et al. Ital J Neurol Sci. 1989 Aug;10(4):433-9. doi: 10.1007/BF02334949. Ital J Neurol Sci. 1989. PMID: 2793417

3

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: mondelli m. Eur Neurol. 1991;31(6):366-71. doi: 10.1159/000116695. Eur Neurol. 1991. PMID: 1661677

4

Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.

Mondelli M, Rossi A, Scarpini C, Guazzi GC. Mondelli M, et al. Electromyogr Clin Neurophysiol. 1995 Nov;35(7):415-24. Electromyogr Clin Neurophysiol. 1995. PMID: 8549432

5

Ataxia-telangiectasia: somatosensory, brainstem auditory and motor evoked potentials in six patients.

Scarpini C, Mondelli M, Guazzi GC, Federico A. Scarpini C, et al. Among authors: mondelli m. Dev Med Child Neurol. 1996 Jan;38(1):65-73. doi: 10.1111/j.1469-8749.1996.tb15034.x. Dev Med Child Neurol. 1996. PMID: 8606018

6

Involvement of peripheral sensory fibers in amyotrophic lateral sclerosis: electrophysiological study of 64 cases.

Mondelli M, Rossi A, Passero S, Guazzi GC. Mondelli M, et al. Muscle Nerve. 1993 Feb;16(2):166-72. doi: 10.1002/mus.880160208. Muscle Nerve. 1993. PMID: 8429840

7

Nemaline myopathy: description of an adult onset case.

Ginanneschi F, Mondelli M, Malandrini A, Gambelli S, Dotti MT, Federico A. Ginanneschi F, et al. Among authors: mondelli m. J Submicrosc Cytol Pathol. 2002 Jan;34(1):105-8. J Submicrosc Cytol Pathol. 2002. PMID: 11989852

8

Mitochondrial alterations in muscle biopsies of patients on statin therapy.

Gambelli S, Dotti MT, Malandrini A, Mondelli M, Stromillo ML, Gaudiano C, Federico A. Gambelli S, et al. Among authors: mondelli m. J Submicrosc Cytol Pathol. 2004 Jan;36(1):85-9. J Submicrosc Cytol Pathol. 2004. PMID: 15311678

9

Axonal motor and sensory neuropathy in myotonic dystrophy.

Mondelli M, Rossi A, Malandrini A, Della Porta P, Guzaai GC. Mondelli M, et al. Acta Neurol Scand. 1993 Aug;88(2):141-8. doi: 10.1111/j.1600-0404.1993.tb04206.x. Acta Neurol Scand. 1993. PMID: 8213059

10

BAEP changes in Leber's hereditary optic atrophy: further confirmation of multisystem involvement.

Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A. Mondelli M, et al. Acta Neurol Scand. 1990 Apr;81(4):349-53. doi: 10.1111/j.1600-0404.1990.tb01569.x. Acta Neurol Scand. 1990. PMID: 2360403

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