Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience by Maguolo, A., Rodella, G., Dianin, A., Nurti, R., Monge, I., Rigotti, E., Cantalupo, G., Salviati, L., Tucci, S., Pellegrini, F., Molinaro, G., Lupi, F., Tonin, P., Pasini, A., Campostrini, N., Ion Popa, F., Teofoli, F., Vincenzi, M., Camilot, M., Piacentini, G., Bordugo, A.

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Genotype in the diagnosis of 21-hydroxylase deficiency: Who should undergo CYP21A2 analysis? by Cavarzere, P., Vincenzi, M., Teofoli, F., Gaudino, R., Lauriola, S., Maines, E., Camilot, M., Antoniazzi, F.

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Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children by Teofoli, F, Camilot, M, Tatò, L

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Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient by Maines, E., Morandi, G., Gugelmo, G., Ion-Popa, F., Campostrini, N., Pasini, A., Vincenzi, M., Teofoli, F., Camilot, M., Bordugo, A.

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Vitamin B 12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient by Maines, E, Morandi, G, Gugelmo, G, Ion-Popa, F, Campostrini, N, Pasini, A, Vincenzi, M, Teofoli, F, Camilot, M, Bordugo, A

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A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis by Camilot, M., Teofoli, F., Longobardi, S., Gandini, A., Lievore, C., Lauriola, S., Tatò, L.

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Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes by Camilot, Marta, Teofoli, Francesca, Gandini, Alberto, Franceschi, Roberto, Rapa, Anna, Corrias, Andrea, Bona, Gianni, Radetti, Giorgio, Tatò, Luciano

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