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Results: 1-5 |
Results: 5

Authors: Di Iorio, G Cappa, V Ciccodicola, A Sampaolo, S Ammendola, A Sanges, G Giugliano, R D'Urso, M
Citation: G. Di Iorio et al., A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease, NEUROL SCI, 21(2), 2000, pp. 109-112

Authors: Zerr, I Brandel, JP Masullo, C Wientjens, D de Silva, R Zeidler, M Granieri, E Sampaolo, S van Duijn, C Delasnerie-Laupretre, N Will, R Poser, S
Citation: I. Zerr et al., European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factors, J CLIN EPID, 53(7), 2000, pp. 747-754

Authors: Sanges, G Sampaolo, S Di Iorio, G
Citation: G. Sanges et al., Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome, J NEUROL, 246(2), 1999, pp. 134-135

Authors: Navarro, JC Kunas, RC Sampaolo, S Mansmann, U
Citation: Jc. Navarro et al., Heart mitochondria in rats submitted to chronic hypoxia, HIST HISTOP, 14(4), 1999, pp. 1045-1052

Authors: Sampaolo, S Puca, AA Nigro, V Cappa, V Sannino, V Sanges, G Bonavita, V Di Iorio, G
Citation: S. Sampaolo et al., Lack of sodium channel mutation in an Italian family with paramyotonia congenita, NEUROLOGY, 53(7), 1999, pp. 1549-1555
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