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Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.
Berkovic SF, Oliver KL, Canafoglia L, Krieger P, Damiano JA, Hildebrand MS, Morbin M, Vears DF, Sofia V, Giuliano L, Garavaglia B, Simonati A, Santorelli FM, Gambardella A, Labate A, Belcastro V, Castellotti B, Ozkara C, Zeman A, Rankin J, Mole SE, Aguglia U, Farrell M, Rajagopalan S, McDougall A, Brammah S, Andermann F, Andermann E, Dahl HM, Franceschetti S, Carpenter S. Berkovic SF, et al. Among authors: aguglia u. Brain. 2019 Jan 1;142(1):59-69. doi: 10.1093/brain/awy297. Brain. 2019. PMID: 30561534
Triphasic waves and cerebral tumors.
Aguglia U, Gambardella A, Oliveri RL, Lavano A, Camerlingo R, Quattrone A. Aguglia U, et al. Eur Neurol. 1990;30(1):1-5. doi: 10.1159/000116614. Eur Neurol. 1990. PMID: 2298220
Nonmetabolic causes of triphasic waves: a reappraisal.
Aguglia U, Gambardella A, Oliveri RL, Lavano A, Quattrone A. Aguglia U, et al. Clin Electroencephalogr. 1990 Jul;21(3):120-5. doi: 10.1177/155005949002100305. Clin Electroencephalogr. 1990. PMID: 2364553
Photic-induced epileptic negative myoclonus: a case report.
Gambardella A, Aguglia U, Oliveri RL, Pucci F, Zappia M, Quattrone A. Gambardella A, et al. Among authors: aguglia u. Epilepsia. 1996 May;37(5):492-4. doi: 10.1111/j.1528-1157.1996.tb00596.x. Epilepsia. 1996. PMID: 8617179
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
Quattrone A, Gambardella A, Bono F, Aguglia U, Bolino A, Bruni AC, Montesi MP, Oliveri RL, Sabatelli M, Tamburrini O, Valentino P, Van Broeckhoven C, Zappia M. Quattrone A, et al. Among authors: aguglia u. Neurology. 1996 May;46(5):1318-24. doi: 10.1212/wnl.46.5.1318. Neurology. 1996. PMID: 8628474
299 results