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Results:
1-8
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Results: 8
Authors:
Bosone, I
Bortolotto, S
Mongini, T
Doriguzzi, C
Chiado-Piat, L
Ugo, I
Mutani, R
Palmucci, L
Citation: I. Bosone et al., Late onset and very mild course of Xp21 Becker type muscular dystrophy, CLIN NEUR, 20(5), 2001, pp. 196-199
Authors:
Mongini, T
Doriguzzi, C
Arduino, C
Brusco, A
Bortolotto, S
Mutani, R
Palmucci, L
Citation: T. Mongini et al., Myopathy in a patient with chromosome 22q11 deletion, NEUROPEDIAT, 32(2), 2001, pp. 107-109
Authors:
Vigliani, MC
Palmucci, L
Polo, P
Mutani, R
Schiffer, D
De Luca, S
De Zan, A
Citation: Mc. Vigliani et al., Paraneoplastic opsoclonus-myoclonus associated with renal cell carcinoma and responsive to tumour ablation, J NE NE PSY, 70(6), 2001, pp. 814-815
Authors:
Silvestri, G
Mongini, T
Odoardi, F
Modoni, A
deRosa, G
Doriguzzi, C
Palmucci, L
Tonali, P
Servidei, S
Citation: G. Silvestri et al., A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency, NEUROLOGY, 54(8), 2000, pp. 1693-1696
Authors:
Palmucci, L
Mongini, T
Chiado-Piat, L
Doriguzzi, C
Fubini, A
Citation: L. Palmucci et al., Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family, NEUROLOGY, 54(2), 2000, pp. 529-530
Authors:
Palmucci, L
Citation: L. Palmucci, The triumphs of the Baroque. Architecture in Europe 1600-1750, STUD PIEMON, 28(2), 1999, pp. 582-585
Authors:
Palmucci, L
Doriguzzi, C
Mongini, T
Chiado-Piat, L
Ugo, I
Citation: L. Palmucci et al., Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathy, EUR NEUROL, 42(4), 1999, pp. 221-224
Authors:
Doriguzzi, C
Palmucci, L
Mongini, T
Chiado-Piat, L
Saggiorato, C
Ugo, I
Hoffman, EP
Citation: C. Doriguzzi et al., Variable histological expression of dystrophinopathy in two females, ACT NEUROP, 97(6), 1999, pp. 657-660
Risultati:
1-8
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