Well Design Challenges in Geothermal Energy Applications von Daniele Farina, Vanessa S. Iorio, Pasquale Mangano, Domenico Santoro, Luca Dal Forno, Carla Sanasi

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A robust upper limit on Neff from BBN, circa 2011 von Mangano, Gianpiero, Serpico, Pasquale D.

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Primordial nucleosynthesis: From precision cosmology to fundamental physics von Iocco, Fabio, Mangano, Gianpiero, Miele, Gennaro, Pisanti, Ofelia, Serpico, Pasquale D.

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Multimomentum and multiflavor active-sterile neutrino oscillations in the early universe: Role of neutrino asymmetries and effects on nucleosynthesis von Saviano, Ninetta, Mirizzi, Alessandro, Pisanti, Ofelia, Serpico, Pasquale Dario, Mangano, Gianpiero, Miele, Gennaro

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Strongest model-independent bound on the lifetime of Dark Matter von Audren, Benjamin, Lesgourgues, Julien, Mangano, Gianpiero, Serpico, Pasquale Dario, Tram, Thomas

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Relic neutrino decoupling including flavour oscillations von Mangano, Gianpiero, Miele, Gennaro, Pastor, Sergio, Pinto, Teguayco, Pisanti, Ofelia, Serpico, Pasquale D.

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De novo GRIN2A variants associated with epilepsy and autism and literature review von Mangano, Giuseppe Donato, Riva, Antonella, Fontana, Antonina, Salpietro, Vincenzo, Mangano, Giuseppa Renata, Nobile, Giulia, Orsini, Alessandro, Iacomino, Michele, Battini, Roberta, Astrea, Guja, Striano, Pasquale, Nardello, Rosaria

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Influence of almond hulls in lamb diets on animal performance and meat quality von Scerra, Manuel, Bognanno, Matteo, Foti, Francesco, Caparra, Pasquale, Cilione, Caterina, Mangano, Fabrizio, Natalello, Antonio, Chies, Luigi

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Macrophage Migration Inhibitory Factor (MIF) and Its Homologue d-Dopachrome Tautomerase (DDT) Inversely Correlate with Inflammation in Discoid Lupus Erythematosus von Caltabiano, Rosario, De Pasquale, Rocco, Piombino, Eliana, Campo, Giorgia, Nicoletti, Ferdinando, Cavalli, Eugenio, Mangano, Katia, Fagone, Paolo

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Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review von Nardello, Rosaria, Mangano, Giuseppe Donato, Antona, Vincenzo, Fontana, Antonina, Striano, Pasquale, Giorgio, Elisa, Brusco, Alfredo, Mangano, Salvatore, Salpietro, Vincenzo

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KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties von Cioclu, Maria Cristina, Mosca, Ilaria, Ambrosino, Paolo, Puzo, Deborah, Bayat, Allan, Wortmann, Saskia B, Koch, Johannes, Strehlow, Vincent, Shirai, Kentaro, Matsumoto, Naomichi, Sanders, Stephan J, Michaud, Vincent, Legendre, Marine, Riva, Antonella, Striano, Pasquale, Muhle, Hiltrud, Pendziwiat, Manuela, Lesca, Gaetan, Mangano, Giuseppe Donato, Nardello, Rosaria, Lemke, Johannes R, Møller, Rikke S, Soldovieri, Maria Virginia, Rubboli, Guido, Taglialatela, Maurizio

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Evaluation of the Involvement of Heme Oxygenase-1 Expression in Discoid Lupus Erythematosus Lesions von Fagone, Paolo, Piombino, Eliana, Mangano, Katia, De Pasquale, Rocco, Nicoletti, Ferdinando, Caltabiano, Rosario

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A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability von Miceli, Francesco, Striano, Pasquale, Soldovieri, Maria Virginia, Fontana, Antonina, Nardello, Rosaria, Robbiano, Angela, Bellini, Giulia, Elia, Maurizio, Zara, Federico, Taglialatela, Maurizio, Mangano, Salvatore

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GRB 130427A: A Nearby Ordinary Monster von Maselli, A., Melandri, A., Nava, L., Mundell, C. G., Kawai, N., Campana, S., Covino, S., Cummings, J. R., Cusumano, G., Evans, P. A., Ghirlanda, G., Ghisellini, G., Guidorzi, C., Kobayashi, S., Kuin, P., La Parola, V., Mangano, V., Oates, S., Sakamoto, T., Serino, M., Virgili, F., Zhang, B.-B., Barthelmy, S., Beardmore, A., Bernardini, M. G., Bersier, D., Burrows, D., Calderone, G., Capalbi, M., Chiang, J., D'Avanzo, P., D'Elia, V., De Pasquale, M., Fugazza, D., Gehrels, N., Gomboc, A., Harrison, R., Hanayama, H., Japelj, J., Kennea, J., Kopac, D., Kouveliotou, C., Kuroda, D., Levan, A., Malesani, D., Marshall, F., Nousek, J., O'Brien, P., Osborne, J. P., Pagani, C., Page, K. L., Page, M., Perri, M., Pritchard, T., Romano, P., Saito, Y., Sbarufatti, B., Salvaterra, R., Steele, I., Tanvir, N., Vianello, G., Weigand, B., Wiersema, K., Yatsu, Y., Yoshii, T., Tagliaferri, G.

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Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification von Schottlaender, Lucia V., Abeti, Rosella, Jaunmuktane, Zane, Macmillan, Carol, Chelban, Viorica, O’Callaghan, Benjamin, McKinley, John, Maroofian, Reza, Efthymiou, Stephanie, Athanasiou-Fragkouli, Alkyoni, Forbes, Raeburn, Soutar, Marc P.M., Livingston, John H., Kalmar, Bernardett, Swayne, Orlando, Hotton, Gary, Groppa, Stanislav, Karashova, Blagovesta Marinova, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez-Dueñas, Belen, Di Rosa, Gabriella, Goraya, Jatinder S., Sultan, Tipu, Mine, Jun, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Banu, Selina, Pineda-Marfa, Mercedes, Veggiotti, Pierangelo, Ferrari, Michel D., Verrotti, Alberto, Marseglia, Giangluigi, Savasta, Salvatore, García-Silva, Mayte, Ruiz, Alfons Macaya, Garavaglia, Barbara, Borgione, Eugenia, Portaro, Simona, Sanchez, Benigno Monteagudo, Boles, Richard, Papacostas, Savvas, Vikelis, Michail, Papanicolaou, Eleni Zamba, Dardiotis, Efthymios, Maqbool, Shazia, Ibrahim, Shahnaz, Kirmani, Salman, Rana, Nuzhat Noureen, Atawneh, Osama, Koutsis, George, Breza, Marianthi, Mangano, Salvatore, Scuderi, Carmela, Morello, Giovanna, Stojkovic, Tanya, Zollo, Massimi, Heimer, Gali, Dauvilliers, Yves A., Striano, Pasquale, Al-Khawaja, Issam, Al-Mutairi, Fuad, Sherifa, Hamed, Pittman, Alan, Mendes de Oliveira, João Ricardo, de Grandis, Maria, Richard-Loendt, Angela, Launchbury, Francesca, Althonayan, Juri, McDonnell, Gavin, Carr, Aisling, Khan, Suliman, Beetz, Christian, Bisgin, Atil, Tug Bozdogan, Sevcan, Begtrup, Amber, Torti, Erin, Greensmith, Linda, Giunti, Paola, Morrison, Patrick J., Brandner, Sebastian, Aurrand-Lions, Michel, Houlden, Henry

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PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation von Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zamba‐Papanicolaou, Eleni, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Kernohan, Kristin D., Eaton, Alison, Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Zetterberg, Henrik, Heales, Simon J. R., Rothman, James E., Clayton, Peter T., Houlden, Henry, Kriouile, Yamna, Aguennouz, Mhammed, Groppa, Stanislav, Marinova Karashova, Blagovesta, Van Maldergem, Lionel, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez‐Dueñas, Belen, Di Rosa, Gabriella, Goraya, Jatinder S., Sultan, Tipu, Mine, Jun, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Pineda‐Marfa, Mercedes, Ferrari, Michel D., van den Maagdenberg, Arn M J M, Verrotti, Alberto, Marseglia, Giangluigi, García‐Silva, Mayte, Ruiz, Alfons Macaya, Garavaglia, Barbara, Borgione, Eugenia, Portaro, Simona, Boles, Richard, Giunti, Paola, Chelban, Viorica, Salpietro, Vincenzo, Efthymiou, Stephanie, Kullmann, Dimitri, Kaiyrzhanov, Rauan, Sullivan, Roisin, Khan, Alaa Matooq, Yau, Wai Yan, Papanicolaou, Eleni Zamba, Maqbool, Shazia, Rana, Nuzhat Noureen, Atawneh, Osama, Shaikh, Farooq, Koutsis, George, Breza, Marianthi, Mangano, Salvatore, Scuderi, Carmela, Borgione, Eugenia, Stojkovic, Tanya, Torti, Erin, Zollo, Massimi, Dauvilliers, Yves A., Rizig, Mie, Okubadejo, Njideka U., Ojo, Oluwadamilola O., Wahab, Kolawole, Bello, Abiodun H., Obiabo, Yahaya, Nwazor, Ernest, Iyagba, Alagoma, Taiwo, Lolade, Komolafe, Morenikeji, Oguntunde, Olapeju, Senkevich, Konstantin, Haridy, Nourelhoda, Shashkin, Chingiz, Zharkynbekova, Nazira, Koneyev, Kairgali, Isrofilov, Maksud, Khachatryan, Samson, Silvestri, Gabriella, Bourinaris, Thomas, Fidani, Liana

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Effects of non-standard neutrino–electron interactions on relic neutrino decoupling von Mangano, Gianpiero, Miele, Gennaro, Pastor, Sergio, Pinto, Teguayco, Pisanti, Ofelia, Serpico, Pasquale D.

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Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome von Salpietro, Vincenzo, Maroofian, Reza, Wangen, Jamie, Ciolfi, Andrea, Barresi, Sabina, Efthymiou, Stephanie, Aughey, Gabriel N., Al Mutairi, Fuad, Accogli, Andrea, Zara, Federico, Tariq, Huma, Rehman, Khalil Ur, Abd Elmaksoud, Marwa, El Said, Huda G., Al Shalan, Maha, Khang, Rin, Elbendary, Hasnaa M., Marinakis, Nikolaos M., Traeger-Synodinos, Joanne, Ververi, Athina, Sourmpi, Mara, Khadivi Zand, Farhad, Beiraghi Toosi, Mehran, Hannah, Michael G., Bertini, Enrico, Aguennouz, Mhammed, Groppa, Stanislav, Kathom, Hadil, Tincheva, Radka, Verrotti, Alberto, Macaya, Alfons, Garavaglia, Barbara, Cortese, Andrea, Sullivan, Roisin, Papanicolaou, Eleni Z., Dardiotis, Efthymios, Maqbool, Shazia, Ibrahim, Shahnaz, Rana, Nuzhat N., Atawneh, Osama, Zuccotti, Gian V., Marseglia, Gian L., Shaikh, Farooq, Corsello, Giovanni, Mangano, Salvatore, Koutsis, George, Scuderi, Carmela, Ferrara, Pietro, Zollo, Massimo, Berni-Canani, Roberto, Sisto, Antonio, Strano, Federica, Di Francesco, Ludovica, Salayev, Kamran, Xiromerisiou, Georgia, Munell, Francina, Gagliano, Antonella, Jan, Farida, Chimenz, Roberto, Di Rosa, Gabriella, Pettoello-Mantovani, Massimo, Tazir, Meriem, Farello, Giovanni, Delvecchio, Maurizio, Di-Donato, Giulio, Obeid, Makram, Saadi, Nebal W., Maccarone, Rita, Kara, Majdi, Karimiani, Ehsan G., Seri, Marco, Di-Falco, Giovanna, Barrano, Giuseppe, Operto, Francesca F., Valenzise, Mariella, Matricardi, Sara, Zafar, Faisal, Ullah, Ehsan, Afzal, Erum, Rahman, Fatima, De Filippo, Maria, Licari, Amelia, Trebbi, Edoardo, Romano, Ferdinando, Heimer, Gali, Al-Khawaja, Issam, Al-Mutairi, Fuad, Shashkin, Chingiz, Koneyev, Kairgali, Pagnamenta, Alistair T., Corsello, Antonio, Dallapiccola, Bruno, Alobeid, Eman, Mankad, Kshitij, Ghayoor-Karimiani, Ehsan, Chung, Wendy K., Green, Rachel, Alkuraya, Fowzan S., Jepson, James E.C., Houlden, Henry

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Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants von Neuray, Caroline, Maroofian, Reza, Scala, Marcello, Sultan, Tipu, Pai, Gurpur S, Mojarrad, Majid, Khashab, Heba El, deHoll, Leigh, Yue, Wyatt, Alsaif, Hessa S, Zanetti, Maria N, Bello, Oscar, Person, Richard, Eslahi, Atieh, Khazaei, Zaynab, Feizabadi, Masoumeh H, Efthymiou, Stephanie, El-Bassyouni, Hala T, Soliman, Doaa R, Tekes, Selahattin, Ozer, Leyla, Baltaci, Volkan, Khan, Suliman, Beetz, Christian, Amr, Khalda S, Salpietro, Vincenzo, Jamshidi, Yalda, Alkuraya, Fowzan S, Houlden, Henry

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Future constraints on neutrino isocurvature perturbations in the curvaton scenario von Di Valentino, Eleonora, Lattanzi, Massimiliano, Mangano, Gianpiero, Melchiorri, Alessandro, Serpico, Pasquale

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