Effect of Pigmented Rice Consumption on Cardiometabolic Risk Factors: A Systematic Review of Randomized Controlled Trials von Mendoza-Sarmiento, Diane, Mistades, Emmanuele V., Hill, Alison M.

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P17.19 Deoxypyrimidine monophosphates treatment for thymidine kinase 2 deficiency von Garone, C, Garcia-Diaz, B, Emmanuele, V, Tadesse, S, Akman, H.O, Tanji, K, Quinzii, C.M, Hirano, M

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P.5.19 Fhl1 W122S knock-in mice manifest late-onset mild myopathy von Emmanuele, V, Kubota, A, Garcia-Diaz, B, Garone, C, Akman, H.O, Tanji, K, Quinzii, C.M, Hirano, M

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Retinopathy screening in patients with Type 1 diabetes diagnosed in young age using a non-mydriatic digital stereoscopic retinal imaging von Minuto, N., Emmanuele, V., Vannati, M., Russo, C., Rebora, C., Panarello, S., Pistorio, A., Lorini, R., d’Annunzio, G.

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CoQ10 supplementation rescues nephrotic syndrome through normalization of H2S oxidation pathway von Kleiner, Giulio, Barca, Emanuele, Ziosi, Marcello, Emmanuele, Valentina, Xu, Yimeng, Hidalgo-Gutierrez, Agustin, Qiao, Changhong, Tadesse, Saba, Area-Gomez, Estela, Lopez, Luis C., Quinzii, Catarina M.

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Remitting symmetrical pitting edema of hands and feet at onset of pediatric systemic lupus erythematosus: a case report von Alpigiani, M G, Giampietri, L, Emmanuele, V, Salvati, P, Valle, M, Lorini, R

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Mothers with their babies in prison: the first Italian experience von Ferrara, P, Emmanuele, V, Nicoletti, A, Mastrangelo, A, Marrone, G, Pedote, G

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Pseudo-dominant inheritance of a novel homozygous HACD1 mutation associated with congenital myopathy: The first caucasian family von Toscano, A., Emmanuele, V., Savarese, M., Musumeci, O., Torella, A., Conca, E., Moggio, M., Nigro, V., Rodolico, C.

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P.260 - Pseudo-dominant inheritance of a novel homozygous HACD1 mutation associated with congenital myopathy: The first caucasian family von Toscano, A., Emmanuele, V., Savarese, M., Musumeci, O., Torella, A., Conca, E., Moggio, M., Nigro, V., Rodolico, C.

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175 Noninvasive ventilation (NIV) in cystic fibrosis patients (CF) with past pneumothorax (PNX): a case report von Casciaro, R, Ottonello, G, DeAlessandri, A, Emmanuele, V, Caso, M, Haupt, M, Minicucci, L, Lorini, L

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MERRF and Kearns-Sayre Overlap Syndrome Due to the Mitochondrial DNA M.3291T>C Mutation (P07.209) von Emmanuele, V., Silvers, D., Sotiriou, E., Tanji, K., DiMauro, S., Hirano, M.

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MERRF and Kearns-Sayre Overlap Syndrome Due to the Mitochondrial DNA M.3291T>C Mutation (IN7-1.008) von Emmanuele, V., Silvers, D., Sotiriou, E., Tanji, K., DiMauro, S., Hirano, M.

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MitoExome Sequencing Reveals a Mutation in the Mitochondrial MRPL51 Gene Causing Infantile Encephalopathy (P05.139) von Garone, C., Calvo, S., Emmanuele, V., Akman, O. H., Kaplan, P., Krishna, S., Mootha, V., DiMauro, S., Hirano, M.

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Potential celiac disease in type 1 diabetes: A multicenter study von Franzese, Adriana, Iafusco, Dario, Spadaro, Raffaella, Cavaliere, Olmina, Prisco, Francesco, Auricchio, Renata, Troncone, Riccardo, Valerio, Giuliana

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Severe Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Due to a New Molecular Defect (P05.135) von Quinzii, C., Barros, M., Sanna-Cherchi, S., Emmanuele, V., Lopez Garcia, B., Akman, A., Horvath, R., Ferreiro-Barros, C., El Gharably, N., De Vivo, D., Shokr, A., Hirano, M.

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Severe Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Due to a New Molecular Defect (IN7-1.003) von Quinzii, C., Barros, M., Sanna-Cherchi, S., Emmanuele, V., Lopez Garcia, B., Akman, A., Horvath, R., Ferreiro-Barros, C., El Gharably, N., De Vivo, D., Shokr, A., Hirano, M.

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Health care of children living with their mother in prison compared with the general population von FERRARA, PIETRO, GATTO, ANTONIO, NICOLETTI, ALESSANDRO, EMMANUELE, VALENTINA, FASANO, ALFONSO, CURRÒ, VINCENZO

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Highly nonlinear trion-polaritons in a monolayer semiconductor von Emmanuele, R. P. A., Sich, M., Kyriienko, O., Shahnazaryan, V., Withers, F., Catanzaro, A., Walker, P. M., Benimetskiy, F. A., Skolnick, M. S., Tartakovskii, A. I., Shelykh, I. A., Krizhanovskii, D. N.

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Remitting symmetrical pitting edema of hands and feet at onset of pediatric systemic lupus erythematosus: a case report von Alpigiani, M G, Giampietri, L, Emmanuele, V, Salvati, P, Valle, M, Lorini, R

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Ultrafast-nonlinear ultraviolet pulse modulation in an AlInGaN polariton waveguide operating up to room temperature von Di Paola, D. M., Walker, P. M., Emmanuele, R. P. A., Yulin, A. V., Ciers, J., Zaidi, Z., Carlin, J.-F., Grandjean, N., Shelykh, I., Skolnick, M. S., Butté, R., Krizhanovskii, D. N.

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