Berti G - Search Results

1

Ultrastructural findings in the peripheral nerve in a family with the intermediate form of Charcot-Marie-Tooth disease.

Malandrini A, Ceuterick C, Villanova M, Gambelli S, Berti G, Rossi A, Guazzi GC. Malandrini A, et al. Among authors: berti g. J Submicrosc Cytol Pathol. 2001 Jan-Apr;33(1-2):59-63. J Submicrosc Cytol Pathol. 2001. PMID: 11686409

2

Reduction of pinocytotic vesicle surface density in cultured bovine aortic endothelial cells. A quantitative ultrastructural freeze-etching study.

Bianciardi G, Berti G, Palummo N, Vatti R, Weber E, Weber G. Bianciardi G, et al. Among authors: berti g. J Submicrosc Cytol Pathol. 1988 Oct;20(4):777-82. J Submicrosc Cytol Pathol. 1988. PMID: 3224342

3

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

4

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. Among authors: berti g. J Neurol Sci. 1994 Jun;124(1):89-94. doi: 10.1016/0022-510x(94)90016-7. J Neurol Sci. 1994. PMID: 7931427

5

Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report. A contribution to the knowledge of the functional pathology of the caudate nucleus.

Malandrini A, Fabrizi GM, Palmeri S, Ciacci G, Salvadori C, Berti G, Bucalossi A, Federico A, Guazzi GC. Malandrini A, et al. Among authors: berti g. Acta Neuropathol. 1993;86(6):651-8. doi: 10.1007/BF00294306. Acta Neuropathol. 1993. PMID: 8310821

6

Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy.

Malandrini A, Cavallaro T, Fabrizi GM, Berti G, Salvestroni R, Salvadori C, Guazzi GC. Malandrini A, et al. Among authors: berti g. Virchows Arch. 1995;427(4):415-21. doi: 10.1007/BF00199391. Virchows Arch. 1995. PMID: 8548127

7

Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis.

Malandrini A, Fabrizi GM, Bartalucci P, Salvadori C, Berti G, Sabò C, Guazzi GC. Malandrini A, et al. Among authors: berti g. Childs Nerv Syst. 1996 Mar;12(3):155-60. doi: 10.1007/BF00266820. Childs Nerv Syst. 1996. PMID: 8697459

8

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: berti g. Acta Neuropathol. 1996;91(2):215-8. doi: 10.1007/s004010050417. Acta Neuropathol. 1996. PMID: 8787158

9

Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological report.

Malandrini A, Palmeri S, Fabrizi GM, Villanova M, Berti G, Salvadori C, Gardini G, Motti L, Solimé F, Guazzi GC. Malandrini A, et al. Among authors: berti g. J Neurol Sci. 1998 Mar 5;155(2):218-21. doi: 10.1016/s0022-510x(98)00014-8. J Neurol Sci. 1998. PMID: 9562272

10

Neuronal intranuclear inclusion disease: neuropathologic study of a case.

Malandrini A, Villanova M, Tripodi S, Palmeri S, Sicurelli F, Parrotta E, Berti G, Salvadori C, Cintorino M, Guazzi GC. Malandrini A, et al. Among authors: berti g. Brain Dev. 1998 Aug;20(5):290-4. doi: 10.1016/s0387-7604(98)00032-1. Brain Dev. 1998. PMID: 9760997

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