Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome von Angius, A., Cossu, S., Uva, P., Oppo, M., Onano, S., Persico, I., Fotia, G., Atzeni, R., Cuccuru, G., Asunis, M., Cucca, F., Pruna, D., Crisponi, L.

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Risk of de novo cancers after transplantation: Results from a cohort of 7217 kidney transplant recipients, Italy 1997–2009 von Piselli, Pierluca, Serraino, Diego, Segoloni, Giuseppe Paolo, Sandrini, Silvio, Piredda, Gian Benedetto, Scolari, Maria Piera, Rigotti, Paolo, Busnach, Ghil, Messa, Piergiorgio, Donati, Donato, Schena, Francesco Paolo, Maresca, Maria Cristina, Tisone, Giuseppe, Veroux, Massimiliano, Sparacino, Vito, Pisani, Francesco, Citterio, Franco

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A Prospective Real-World Study of Bacillus clausii Evaluating Use, Treatment Habits and Patient Satisfaction in Italian Community Pharmacies: The PEGASO Study von Giua, Corrado, Romano, Flora, Keber, Enrico, Pellegrino, Paolo, Perez, Marcos, Uboldi, Maria Chiara

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Increased cancer risk in patients undergoing dialysis: a population-based cohort study in North-Eastern Italy von Taborelli, Martina, Toffolutti, Federica, Del Zotto, Stefania, Clagnan, Elena, Furian, Lucrezia, Piselli, Pierluca, Citterio, Franco, Zanier, Loris, Boscutti, Giuliano, Serraino, Diego

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Pneumonia in solid organ transplant recipients: a prospective multicenter study von Giannella, M., Muñoz, P., Alarcón, J.M., Mularoni, A., Grossi, P., Bouza, E.

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THREE-DIMENSIONAL LTCC PACKAGE STRUCTURE von ONANO INDUSTRIAL CORP

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METHOD FOR MANUFACTURING A THREE-DIMENSIONAL LTCC PACKAGE STRUCTURE von ONANO INDUSTRIAL CORP

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THREE-DIMENSIONAL LTCC PACKAGE STRUCTURE von ONANO INDUSTRIAL CORP

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INTEGRATED STRUCTURE OF CIRCUIT MOLD UNIT OF LTCC ELECTRONIC DEVICE von ONANO INDUSTRIAL CORP

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LTCC ELECTRONIC DEVICE UNIT STRUCTURE von ONANO INDUSTRIAL CORP

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Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses von Angius, A, Uva, P, Oppo, M, Buers, I, Persico, I, Onano, S, Cuccuru, G, Van Allen, MI, Hulait, G, Aubertin, G, Muntoni, F, Fry, AE, Annerén, G, Stattin, E-L, Palomares-Bralo, M, Santos-Simarro, F, Cucca, F, Crisponi, G, Rutsch, F, Crisponi, L

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Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome von Angius, A, Cossu, S, Uva, P, Oppo, M, Onano, S, Persico, I, Fotia, G, Atzeni, R, Cuccuru, G, Asunis, M, Cucca, F, Pruna, D, Crisponi, L

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Toothbrush von O'NANO ORAL SOLUTIONS, INC

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Complex genetic signatures in immune cells underlie autoimmunity and inform therapy von Orrù, Valeria, Steri, Maristella, Sidore, Carlo, Marongiu, Michele, Serra, Valentina, Olla, Stefania, Sole, Gabriella, Lai, Sandra, Dei, Mariano, Mulas, Antonella, Virdis, Francesca, Piras, Maria Grazia, Lobina, Monia, Marongiu, Mara, Pitzalis, Maristella, Deidda, Francesca, Loizedda, Annalisa, Onano, Stefano, Zoledziewska, Magdalena, Sawcer, Stephen, Devoto, Marcella, Gorospe, Myriam, Abecasis, Gonçalo R., Floris, Matteo, Pala, Mauro, Schlessinger, David, Fiorillo, Edoardo, Cucca, Francesco

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The eQTLs Catalog and LinDA Browser: A Platform for Determining the Effects on Transcription of GWAS Variants von Pala, Mauro, Onano, Stefano, Cucca, Francesco

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Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report von Alves, Rita Maria, Uva, Paolo, Veiga, Marielza F, Oppo, Manuela, Zschaber, Fabiana C R, Porcu, Giampiero, Porto, Henrique P, Persico, Ivana, Onano, Stefano, Cuccuru, Gianmauro, Atzeni, Rossano, Vieira, Lauro C N, Pires, Marcos V A, Cucca, Francesco, Toralles, Maria Betânia P, Angius, Andrea, Crisponi, Laura

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Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP von Angius, Andrea, Uva, Paolo, Oppo, Manuela, Persico, Ivana, Onano, Stefano, Olla, Stefania, Pes, Valentina, Perria, Chiara, Cuccuru, Gianmauro, Atzeni, Rossano, Serra, Gigliola, Cucca, Francesco, Sotgiu, Stefano, Hennekam, Raoul C., Crisponi, Laura

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Author Correction: Complex genetic signatures in immune cells underlie autoimmunity and inform therapy von Orrù, Valeria, Steri, Maristella, Sidore, Carlo, Marongiu, Michele, Serra, Valentina, Olla, Stefania, Sole, Gabriella, Lai, Sandra, Dei, Mariano, Mulas, Antonella, Virdis, Francesca, Piras, Maria Grazia, Lobina, Monia, Marongiu, Mara, Pitzalis, Maristella, Deidda, Francesca, Loizedda, Annalisa, Onano, Stefano, Zoledziewska, Magdalena, Sawcer, Stephen, Devoto, Marcella, Gorospe, Myriam, Abecasis, Gonçalo R., Floris, Matteo, Pala, Mauro, Schlessinger, David, Fiorillo, Edoardo, Cucca, Francesco

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Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa von Angius, Andrea, Uva, Paolo, Buers, Insa, Oppo, Manuela, Puddu, Alessandro, Onano, Stefano, Persico, Ivana, Loi, Angela, Marcia, Loredana, Höhne, Wolfgang, Cuccuru, Gianmauro, Fotia, Giorgio, Deiana, Manila, Marongiu, Mara, Atalay, Hatice Tuba, Inan, Sibel, El Assy, Osama, Smit, Leo M.E., Okur, Ilyas, Boduroglu, Koray, Utine, Gülen Eda, Kılıç, Esra, Zampino, Giuseppe, Crisponi, Giangiorgio, Crisponi, Laura, Rutsch, Frank

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Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa von Angius, Andrea, Uva, Paolo, Buers, Insa, Oppo, Manuela, Puddu, Alessandro, Onano, Stefano, Persico, Ivana, Loi, Angela, Marcia, Loredana, Höhne, Wolfgang, Cuccuru, Gianmauro, Fotia, Giorgio, Deiana, Manila, Marongiu, Mara, Atalay, Hatice Tuba, Inan, Sibel, El Assy, Osama, Smit, Leo M.E., Okur, Ilyas, Boduroglu, Koray, Utine, Gülen Eda, Kılıç, Esra, Zampino, Giuseppe, Crisponi, Giangiorgio, Crisponi, Laura, Rutsch, Frank

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