Sökresultat - Colombo, Carlo

The Action of the Waters of Fiuggi, Italy av Colombo, Carlo

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Restoration and Enhancement of Historical Stereo Photos † av Fanfani, Marco, Colombo, Carlo, Bellavia, Fabio

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Hyperglucagonemia in an animal model of insulin- deficient diabetes: what therapy can improve it? av Barbetti, Fabrizio, Colombo, Carlo, Haataja, Leena, Cras-Méneur, Corentin, Bernardini, Sergio, Arvan, Peter

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The G53D Mutation in Kir6.2 (KCNJ11) Is Associated with Neonatal Diabetes and Motor Dysfunction in Adulthood that Is Improved with Sulfonylurea Therapy av Koster, Joseph C., Cadario, Francesco, Peruzzi, Cinzia, Colombo, Carlo, Nichols, Colin G., Barbetti, Fabrizio

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Functional Characterization of a Novel KCNJ11 in Frame Mutation-Deletion Associated with Infancy-Onset Diabetes and a Mild Form of Intermediate DEND: A Battle between K(ATP) Gain o... av Lin, Yu-Wen, Li, Anlong, Grasso, Valeria, Battaglia, Domenica, Crinò, Antonino, Colombo, Carlo, Barbetti, Fabrizio, Nichols, Colin G.

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Insulin Gene Mutations as Cause of Diabetes in Children Negative for Five Type 1 Diabetes Autoantibodies av Bonfanti, Riccardo, Colombo, Carlo, Nocerino, Valentina, Massa, Ornella, Lampasona, Vito, Iafusco, Dario, Viscardi, Matteo, Chiumello, Giuseppe, Meschi, Franco, Barbetti, Fabrizio

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Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation av Battaglia, Domenica, Lin, Yu-Wen, Brogna, Claudia, Crinò, Antonino, Grasso, Valeria, Mozzi, Alessia F, Russo, Lucia, Spera, Sabrina, Colombo, Carlo, Ricci, Stefano, Nichols, Colin G, Mercuri, Eugenio, Barbetti, Fabrizio

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Congenital Hyperinsulinism and Glucose Hypersensitivity in Homozygous and Heterozygous Carriers of Kir6.2 (KCNJ11) Mutation V290M Mutation: K(ATP) Channel Inactivation Mechanism an... av Loechner, Karen J., Akrouh, Alejandro, Kurata, Harley T., Dionisi-Vici, Carlo, Maiorana, Arianna, Pizzoferro, Milena, Rufini, Vittoria, de Ville de Goyet, Jean, Colombo, Carlo, Barbetti, Fabrizio, Koster, Joseph C., Nichols, Colin G.

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Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus av Colombo, Carlo, Porzio, Ottavia, Liu, Ming, Massa, Ornella, Vasta, Mario, Salardi, Silvana, Beccaria, Luciano, Monciotti, Carla, Toni, Sonia, Pedersen, Oluf, Hansen, Torben, Federici, Luca, Pesavento, Roberta, Cadario, Francesco, Federici, Giorgio, Ghirri, Paolo, Arvan, Peter, Iafusco, Dario, Barbetti, Fabrizio

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Opposite Clinical Phenotypes of Glucokinase Disease: Description of a Novel Activating Mutation and Contiguous Inactivating Mutations in Human Glucokinase (GCK) Gene av Barbetti, Fabrizio, Cobo-Vuilleumier, Nadia, Dionisi-Vici, Carlo, Toni, Sonia, Ciampalini, Paolo, Massa, Ornella, Rodriguez-Bada, Pablo, Colombo, Carlo, Lenzi, Lorenzo, Garcia-Gimeno, María A., Bermudez-Silva, Francisco J., Rodriguez de Fonseca, Fernando, Banin, Patrizia, Aledo, Juan C., Baixeras, Elena, Sanz, Pascual, Cuesta-Muñoz, Antonio L.

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