Groundwater Quality Assessment Based on Water Quality Index in Northern Cyprus
Kassem, Y., Gökçekuş, H., Rizza, T.
Published in Engineering, technology & applied science research (01.04.2022)
Published in Engineering, technology & applied science research (01.04.2022)
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Journal Article
Novel mutations in KARS cause hypertrophic cardiomyopathy and combined mitochondrial respiratory chain defect
Verrigni, D., Diodato, D., Di Nottia, M., Torraco, A., Bellacchio, E., Rizza, T., Tozzi, G., Verardo, M., Piemonte, F., Tasca, G., D'Amico, A., Bertini, E., Carrozzo, R.
Published in Clinical genetics (01.06.2017)
Published in Clinical genetics (01.06.2017)
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Journal Article
DJ‐1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7
Di Nottia, M., Masciullo, M., Verrigni, D., Petrillo, S., Modoni, A., Rizzo, V., Di Giuda, D., Rizza, T., Niceta, M., Torraco, A., Bianchi, M., Santoro, M., Bentivoglio, A.R., Bertini, E., Piemonte, F., Carrozzo, R., Silvestri, G.
Published in Clinical genetics (01.07.2017)
Published in Clinical genetics (01.07.2017)
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Journal Article
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia
Torraco, A., Bianchi, M., Verrigni, D., Gelmetti, V., Riley, L., Niceta, M., Martinelli, D., Montanari, A., Guo, Y., Rizza, T., Diodato, D., Di Nottia, M., Lucarelli, B., Sorrentino, F., Piemonte, F., Francisci, S., Tartaglia, M., Valente, E.M., Dionisi‐Vici, C., Christodoulou, J., Bertini, E., Carrozzo, R.
Published in Clinical genetics (01.03.2017)
Published in Clinical genetics (01.03.2017)
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Journal Article
Distal spinal muscular atrophy and ataxia with cerebellar atrophy in two unrelated patients; a new phenotypic variant of HRD and recessive KCS syndrome related to TBCE
Bertini, E, Sferra, A, Rizza, T, Tasca, G, D'Amico, A, Zanni, G, Barresi, S, Diodato, D, Piermarini, E, Martinelli, D, Dionisi-Vici, C, Niceta, M, Dallapiccola, B, Tartaglia, M, Compagnucci, C
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Journal Article
Mutation analysis in 16 patients with mtDNA depletion
Carrozzo, R., Bornstein, B., Lucioli, S., Campos, Y., de la Pena, P., Petit, N., Dionisi-Vici, C., Vilarinho, L., Rizza, T., Bertini, E., Garesse, R., Santorelli, F.M., Arenas, J.
Published in Human mutation (01.04.2003)
Published in Human mutation (01.04.2003)
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Journal Article
EM.P.5.07 Abnormal elastin deposits and altered organization of elastic fibers in collagen VI- related disorders
Petrini, S, Sabatelli, P, d’Amico, A, Gualandi, F, Braghetta, P, Coccetti, M, Rizza, T, Carrozzo, R, Pepe, G, Bonaldo, P, Ferlini, A, Merlini, L, Bertini, E
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Journal Article
A mitochondrial ATPase 6 mutation is associated with Leigh syndrome in a family and affects proton flow and adenosine triphosphate output when modeled in Escherichia coli
Carrozzo, R, Rizza, T, Lucioli, S, Pierini, R, Bertini, E, Santorelli, FM
Published in Acta Paediatrica (01.04.2004)
Published in Acta Paediatrica (01.04.2004)
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Journal Article
M.P.1.04 A novel mtDNA mutation in COIII impairs assembly of cytochrome c oxidase in a MELAS patient
Tessa, A, Pennisi, E, Cassandrini, D, Rizza, T, Wittig, I, Fattori, F, Meschini, M, Bertini, E, Santarelli, L, Bruno, C, Carrozzo, R, Schägger, H, Santorelli, F
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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Journal Article
Relationship of PROP (6-n-propylthiouracil) taster status with body mass index, food preferences, and consumption of Filipino adolescents
Borazon, Elaine Q., Villarino, Blanca J., Magbuhat, Rizza Marie T., Sabandal, Maria Lourdes
Published in Food research international (01.07.2012)
Published in Food research international (01.07.2012)
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Journal Article
Conference Proceeding
LokaLTE: 600 MHz Community LTE Networks for Rural Areas in the Philippines
Hilario, Calvin Artemies G., Claire Barela, Mary, De Guzman, Mar Francis D., Loquias, Rizza T., Raro, Ramon Vann Cleff B., Quitayen, Jean Jay J., Marciano, Joel Joseph S.
Published in 2020 IEEE Global Humanitarian Technology Conference (GHTC) (29.10.2020)
Published in 2020 IEEE Global Humanitarian Technology Conference (GHTC) (29.10.2020)
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Conference Proceeding
Quantitative Assessment of TV White Space in the Western Philippine Nautical Highway
Loquias, Rizza T., Hilario, Calvin Artemies G., Guzman, Mar Francis D. de, Marciano, Joel Joseph S.
Published in 2019 IEEE International Symposium on Dynamic Spectrum Access Networks (DySPAN) (01.11.2019)
Published in 2019 IEEE International Symposium on Dynamic Spectrum Access Networks (DySPAN) (01.11.2019)
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Conference Proceeding
Replication studies in longevity: puzzling findings in Danish centenarians at the 3′APOB–VNTR locus
VARCASIA, O., GARASTO, S., RIZZA, T., ANDERSEN‐RANBERG, K., JEUNE, B., BATHUM, L., ANDREEV, K., TAN, Q., YASHIN, A. I., BONAFÈ, M., FRANCESCHI, C., BENEDICTIS, G.
Published in Annals of human genetics (01.07.2001)
Published in Annals of human genetics (01.07.2001)
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Journal Article
G.P.123 - Distal spinal muscular atrophy and ataxia with cerebellar atrophy in two unrelated patients; a new phenotypic variant of HRD and recessive KCS syndrome related to TBCE
Bertini, E., Sferra, A., Rizza, T., Tasca, G., D'Amico, A., Zanni, G., Barresi, S., Diodato, D., Piermarini, E., Martinelli, D., Dionisi-Vici, C., Niceta, M., Dallapiccola, B., Tartaglia, M., Compagnucci, C.
Published in Neuromuscular disorders : NMD (01.10.2015)
Published in Neuromuscular disorders : NMD (01.10.2015)
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Journal Article
Maternally‐inherited Leigh syndrome‐related mutations bolster mitochondrial‐mediated apoptosis
Carrozzo, Rosalba, Rizza, Teresa, Stringaro, Annarita, Pierini, Roberta, Mormone, Elisabetta, Santorelli, Filippo M., Malorni, Walter, Matarrese, Paola
Published in Journal of neurochemistry (01.07.2004)
Published in Journal of neurochemistry (01.07.2004)
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Journal Article
Human melanoma/NG2 chondroitin sulfate proteoglycan is expressed in the sarcolemma of postnatal human skeletal myofibers: Abnormal expression in merosin-negative and Duchenne muscular dystrophies
Petrini, Stefania, Tessa, Alessandra, Carrozzo, Rosalba, Verardo, Margherita, Pierini, Roberta, Rizza, Teresa, Bertini, Enrico
Published in Molecular and cellular neuroscience (01.06.2003)
Published in Molecular and cellular neuroscience (01.06.2003)
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Journal Article