MTHFR C677T homozygous as risk factor for complications after OLT for cryptogenic cirrhosis
Pasta, Linda, Marrone, Ciro, D'Amico, Mario, Verdone, Roberto, Rizzo, Aroldo, Sammarco, Piero, Fabiano, Carmelo, Niceta, Marcello, Caltagirone, Maria, D'Amico, Gennaro, Pagliaro, Luigi
Published in Clinical transplantation (01.11.2006)
Published in Clinical transplantation (01.11.2006)
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Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation
Mancuso, Michelangelo, Ferraris, Silvio, Nishigaki, Yutaka, Azan, Gaetano, Mauro, Alessandro, Sammarco, Piero, Krishna, Sindu, Tay, Stacey K.H., Bonilla, Eduardo, Romansky, Stephen G., Hirano, Michio, DiMauro, Salvatore
Published in Journal of the neurological sciences (15.01.2005)
Published in Journal of the neurological sciences (15.01.2005)
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Identification of a new nonsense mutation (Tyr129Stop) of the SRY gene in a newborn infant with XY sex-reversal
Giuffrè, Mario, Sammarco, Piero, Fabiano, Carmelo, Giardina, Fabio, Lunetta, Fabio, Corsello, Giovanni
Published in American journal of medical genetics. Part A (01.07.2004)
Published in American journal of medical genetics. Part A (01.07.2004)
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Effects of methylfolate in the treatment of heterozygous beta-thalassemia patients
Maggio, Aurelio, Siciliano, Salvatore, Calabrese, Nino, Abate, Ida, Di Trapani, Francesca, Marino, Marisa, Sammarco, Piero, Travia, Aurora, Di Libertò, Giuseppe
Published in Current therapeutic research (01.12.1994)
Published in Current therapeutic research (01.12.1994)
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