Infections after T-replete haploidentical transplantation and high-dose cyclophosphamide as graft-versus-host disease prophylaxis by Crocchiolo, R., Bramanti, S., Vai, A., Sarina, B., Mineri, R., Casari, E., Tordato, F., Mauro, E., Timofeeva, I., Lugli, E., Mavilio, D., Carlo-Stella, C., Santoro, A., Castagna, L.

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Ethylmalonic encephalopathy: application of improved biochemical and molecular diagnostic approaches by Drousiotou, A, DiMeo, I, Mineri, R, Georgiou, Th, Stylianidou, G, Tiranti, V

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ETHE1 mutations are specific to ethylmalonic encephalopathy by Tiranti, V, Briem, E, Lamantea, E, Mineri, R, Papaleo, E, Gioia, L De, Forlani, F, Rinaldo, P, Dickson, P, Abu-Libdeh, B, Cindro-Heberle, L, Owaidha, M, Jack, R M, Christensen, E, Burlina, A, Zeviani, M

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Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families by Mariotti, C, Gellera, C, Rimoldi, M, Mineri, R, Uziel, G, Zorzi, G, Pareyson, D, Piccolo, G, Gambi, D, Piacentini, S, Squitieri, F, Capra, R, Castellotti, B, Di Donato, S

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Ethylmalonic Encephalopathy Is Caused by Mutations in ETHE1, a Gene Encoding a Mitochondrial Matrix Protein by Tiranti, Valeria, D’Adamo, Pio, Briem, Egill, Ferrari, Gianfrancesco, Mineri, Rossana, Lamantea, Eleonora, Mandel, Hanna, Balestri, Paolo, Garcia-Silva, Maria-Teresa, Vollmer, Brigitte, Rinaldo, Piero, Hahn, Si Houn, Leonard, James, Rahman, Shamima, Dionisi-Vici, Carlo, Garavaglia, Barbara, Gasparini, Paolo, Zeviani, Massimo

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Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families by Mariotti, C., Gellera, C., Rimoldi, M., Mineri, R., Uziel, G., Zorzi, G., Pareyson, D., Piccolo, G., Gambi, D., Piacentini, S., Squitieri, F., Capra, R., Castellotti, B., Di Donato, S.

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