ΔFosB Regulates Gene Expression and Cognitive Dysfunction in a Mouse Model of Alzheimer’s Disease
Corbett, Brian F., You, Jason C., Zhang, Xiaohong, Pyfer, Mark S., Tosi, Umberto, Iascone, Daniel M., Petrof, Iraklis, Hazra, Anupam, Fu, Chia-Hsuan, Stephens, Gabriel S., Ashok, Annie A., Aschmies, Suzan, Zhao, Lijuan, Nestler, Eric J., Chin, Jeannie
Published in Cell reports (Cambridge) (11.07.2017)
Published in Cell reports (Cambridge) (11.07.2017)
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Identification of de novo mutations and rare variants in hypoplastic left heart syndrome
Iascone, M, Ciccone, R, Galletti, L, Marchetti, D, Seddio, F, Lincesso, AR, Pezzoli, L, Vetro, A, Barachetti, D, Boni, L, Federici, D, Soto, AM, Comas, JV, Ferrazzi, P, Zuffardi, O
Published in Clinical genetics (01.06.2012)
Published in Clinical genetics (01.06.2012)
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A novel homozygous disruptive PRF1 variant (K285Sfs4) causes very early-onset of familial hemophagocytic lymphohystiocytosis type 2
Saettini, F., Castelli, I., Provenzi, M., Fazio, G., Quadri, M., Cazzaniga, G., Sala, S., Dell'Acqua, F., Sieni, E., Coniglio, M. L., Pezzoli, L., Iascone, M., Vendemini, F., Balduzzi, A. C., Biondi, A., Rizzari, C., Bonanomi, S.
Published in Pediatric hematology and oncology (01.03.2021)
Published in Pediatric hematology and oncology (01.03.2021)
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Clinical and molecular characterization of two patients with palmoplantar keratoderma-congenital alopecia syndrome type 2
Castori, M., Morlino, S., Sana, M. E., Paradisi, M., Tadini, G., Angioni, A., Malacarne, M., Grammatico, P., Iascone, M., Forzano, F.
Published in Clinical and experimental dermatology (01.08.2016)
Published in Clinical and experimental dermatology (01.08.2016)
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McCune Albright syndrome and neonatal cholestasis: A new association
Liccardo, D, Pietrobattista, A, Candusso, M, Cardile, S, Basso, M.S, De Vito, R, Iascone, M, Riminucci, M, Torre, G
Published in Digestive and liver disease (08.10.2015)
Published in Digestive and liver disease (08.10.2015)
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Differential pattern of myocardial remodelling in genetically determined and load-dependent hypertrophy in humans
Gervasi, A, Mangiaracina, C, Madeddu, D, Frati, C, Graiani, G, Falco, A, Cavalli, S, Lorusso, B, Rossetti, P, Lagrasta, C.A, Urbanek, K, Quaini, E, Ferrazzi, P, Iascone, M, Quaini, F
Published in Vascular pharmacology (01.12.2015)
Published in Vascular pharmacology (01.12.2015)
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Spinal muscular atrophy: from tissue specificity to therapeutic strategies
Iascone, Daniel M, Henderson, Christopher E, Lee, Justin C
Published in F1000 prime reports (05.01.2015)
Published in F1000 prime reports (05.01.2015)
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De novo Deletion of 1q31.1–q32.1 in a Patient with Developmental Delay and Behavioral Disorders
Milani, D., Bedeschi, M.F., Iascone, M., Chiarelli, G., Cerutti, M., Menni, F.
Published in Cytogenetic and genome research (01.04.2012)
Published in Cytogenetic and genome research (01.04.2012)
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Measurement of brain natriuretic peptide in plasma samples and cardiac tissue extracts by means of an immunoradiometric assay method
DEL RY, S, CLERICO, A, GIANNESSI, D, ANDREASSI, M. G, CAPRIOLI, R, IASCONE, M. R, FERRAZZI, P, BIAGINI, A
Published in Scandinavian journal of clinical and laboratory investigation (2000)
Published in Scandinavian journal of clinical and laboratory investigation (2000)
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Molecular Characterization of Chromosome 22 Deletions by Short Tandem Repeat Polymorphism (STRP) in Patients with Conotruncal Heart Defects
Vittorini, Simona, Sacchelli, Monica, Iascone, Maria R., Collavoli, Anita, Storti, Simona, Giusti, Andrea, Andreani, Giovanna, Botto, Nicoletta, Biagini, Andrea, Clerico, Aldo
Published in Clinical chemistry and laboratory medicine (01.12.2001)
Published in Clinical chemistry and laboratory medicine (01.12.2001)
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A rapid procedure for the quantitation of natriuretic peptide RNAs by competitive RT-PCR in congenital heart defects
IASCONE, M. R, VITTORINI, S, COLLAVOLI, A, CUPELLI, A, KRAFT, G, BIAGINI, A, CLERICO, A
Published in Journal of endocrinological investigation (01.12.1999)
Published in Journal of endocrinological investigation (01.12.1999)
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Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
Crotti, Lia, Spazzolini, Carla, Nyegaard, Mette, Overgaard, Michael T, Kotta, Maria-Christina, Dagradi, Federica, Sala, Luca, Aiba, Takeshi, Ayers, Mark D, Baban, Anwar, Barc, Julien, Beach, Cheyenne M, Behr, Elijah R, Bos, J Martijn, Cerrone, Marina, Covi, Peter, Cuneo, Bettina, Denjoy, Isabelle, Donner, Birgit, Elbert, Adrienne, Eliasson, Håkan, Etheridge, Susan P, Fukuyama, Megumi, Girolami, Francesca, Hamilton, Robert, Horie, Minoru, Iascone, Maria, Jaimez, Juan Jiménez, Jensen, Henrik Kjærulf, Kannankeril, Prince J, Kaski, Juan P, Makita, Naomasa, Muñoz-Esparza, Carmen, Odland, Hans H, Ohno, Seiko, Papagiannis, John, Porretta, Alessandra Pia, Prandstetter, Christopher, Probst, Vincent, Robyns, Tomas, Rosenthal, Eric, Rosés-Noguer, Ferran, Sekarski, Nicole, Singh, Anoop, Spentzou, Georgia, Stute, Fridrike, Tfelt-Hansen, Jacob, Till, Jan, Tobert, Kathryn E, Vinocur, Jeffrey M, Webster, Gregory, Wilde, Arthur A M, Wolf, Cordula M, Ackerman, Michael J, Schwartz, Peter J
Published in European heart journal (14.09.2023)
Published in European heart journal (14.09.2023)
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A contemporary European experience with surgical septal myectomy in hypertrophic cardiomyopathy
IACOVONI, Attilio, SPIRITO, Paolo, FERRAZZI, Paolo, SIMON, Caterina, IASCONE, Maria, DEDDA, Giovanni Di, FILIPPO, Paolo De, PENTIRICCI, Samuele, BONI, Luca, SENNI, Michele, GAVAZZI, Antonello
Published in European heart journal (01.08.2012)
Published in European heart journal (01.08.2012)
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