Hasil Pencarian - Anna-Maria DiBlasio

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  1. 1
    NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis.

    NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis. oleh Davide Gentilini, Antonino Oliveri, Teresa Fazia, Alessandro Pini, Susan Marelli, Luisa Bernardinelli, Anna Maria Di Blasio

    Diterbitkan 2019-01-01
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  2. 2
    Serum Adiponectin Levels in Advanced-Stage Parkinson's Disease Patients

    Serum Adiponectin Levels in Advanced-Stage Parkinson's Disease Patients oleh Erica Cassani, Raffaella Cancello, Ferruccio Cavanna, Sabrina Maestrini, Anna Maria Di Blasio, Antonio Liuzzi, Gianni Pezzoli, Michela Barichella

    Diterbitkan 2011-01-01
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  3. 3
    Differences in visceral fat and fat bacterial colonization between ulcerative colitis and Crohn's disease. An in vivo and in vitro study.

    Differences in visceral fat and fat bacterial colonization between ulcerative colitis and Crohn's disease. An in vivo and in vitro study. oleh Alessandra Zulian, Raffaella Cancello, Chiara Ruocco, Davide Gentilini, Anna Maria Di Blasio, Piergiorgio Danelli, Giancarlo Micheletto, Elisabetta Cesana, Cecilia Invitti

    Diterbitkan 2013-01-01
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  4. 4
    Epigenome Wide Association and Stochastic Epigenetic Mutation Analysis on Cord Blood of Preterm Birth

    Epigenome Wide Association and Stochastic Epigenetic Mutation Analysis on Cord Blood of Preterm Birth oleh Elena Spada, Luciano Calzari, Luigi Corsaro, Teresa Fazia, Monica Mencarelli, Anna Maria Di Blasio, Luisa Bernardinelli, Giulia Zangheri, Michele Vignali, Davide Gentilini

    Diterbitkan 2020-07-01
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  5. 5
    Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome

    Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome oleh Luciano Calzari, Lucia Zanotti, Elvira Inglese, Francesco Scaglione, Rebecca Cavagnola, Francesco Ranucci, Anna Maria Di Blasio, Giulio Stefanini, Gaetano Carlo, Gianfranco Parati, Davide Gentilini

    Diterbitkan 2023-02-01
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  6. 6
    The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report

    The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report oleh Alessandro Cattoni, Alice Spano, Anna Tulone, Annalisa Boneschi, Nicoletta Masera, Silvia Maitz, Anna Maria Di Blasio, Luca Persani, Luca Persani, Fabiana Guizzardi, Fabiana Guizzardi, Raffaella Rossetti

    Diterbitkan 2020-09-01
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  7. 7
    Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations

    Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations oleh Elisa Adele Colombo, Hatice Mutlu-Albayrak, Yousef Shafeghati, Mine Balasar, Juliette Piard, Davide Gentilini, Davide Gentilini, Anna Maria Di Blasio, Cristina Gervasini, Lionel Van Maldergem, Lidia Larizza

    Diterbitkan 2019-05-01
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  8. 8
    Biventricular Arrhythmogenic Cardiomyopathy: a paradigmatic case

    Biventricular Arrhythmogenic Cardiomyopathy: a paradigmatic case oleh camilla torlasco, Franco Cecchi, P. J. Schwartz, G. Parati, L. Crotti, federica dagradi, Barbara Bilo, G. Perego, M. Revera, Anna Maria Di Blasio, Maria-Christina Kotta, Alice Ghidoni, Giulia Girardengo, Margherita Calcagnino

    Diterbitkan 2015-01-01
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  9. 9
    Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients

    Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients oleh Melania Lippi, Mattia Chiesa, Ciro Ascione, Matteo Pedrazzini, Saima Mushtaq, Davide Rovina, Daniela Riggio, Anna Maria Di Blasio, Maria Luisa Biondi, Giulio Pompilio, Gualtiero I. Colombo, Michela Casella, Valeria Novelli, Elena Sommariva

    Diterbitkan 2022-07-01
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  10. 10
    Genomic adaptations to cereal‐based diets contribute to mitigate metabolic risk in some human populations of East Asian ancestry

    Genomic adaptations to cereal‐based diets contribute to mitigate metabolic risk in some human populations of East Asian ancestry oleh Arianna Landini, Shaobo Yu, Guido Alberto Gnecchi‐Ruscone, Paolo Abondio, Claudia Ojeda‐Granados, Stefania Sarno, Sara De Fanti, Davide Gentilini, Anna Maria Di Blasio, Hanjun Jin, Thanh Tin Nguyen, Giovanni Romeo, Cecilia Prata, Eugenio Bortolini, Donata Luiselli, Davide Pettener, Marco Sazzini

    Diterbitkan 2021-02-01
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  11. 11
    An overview of the genetic structure within the Italian population from genome-wide data.

    An overview of the genetic structure within the Italian population from genome-wide data. oleh Cornelia Di Gaetano, Floriana Voglino, Simonetta Guarrera, Giovanni Fiorito, Fabio Rosa, Anna Maria Di Blasio, Paola Manzini, Irma Dianzani, Marta Betti, Marta Betti, Daniele Cusi, Francesca Frau, Cristina Barlassina, Dario Mirabelli, Corrado Magnani, Nicola Glorioso, Stefano Bonassi, Alberto Piazza, Giuseppe Matullo

    Diterbitkan 2012-01-01
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  12. 12
    Genome-wide DNA promoter methylation and transcriptome analysis in human adipose tissue unravels novel candidate genes for obesity

    Genome-wide DNA promoter methylation and transcriptome analysis in human adipose tissue unravels novel candidate genes for obesity oleh Maria Keller, Lydia Hopp, Xuanshi Liu, Tobias Wohland, Kerstin Rohde, Raffaella Cancello, Matthias Klös, Karl Bacos, Matthias Kern, Fabian Eichelmann, Arne Dietrich, Michael R. Schön, Daniel Gärtner, Tobias Lohmann, Miriam Dreßler, Michael Stumvoll, Peter Kovacs, Anna-Maria DiBlasio, Charlotte Ling, Hans Binder, Matthias Blüher, Yvonne Böttcher

    Diterbitkan 2017-01-01
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  13. 13
    Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.

    Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. oleh Sandosh Padmanabhan, Olle Melander, Toby Johnson, Anna Maria Di Blasio, Wai K Lee, Davide Gentilini, Claire E Hastie, Cristina Menni, Maria Cristina Monti, Christian Delles, Stewart Laing, Barbara Corso, Gerjan Navis, Arjan J Kwakernaak, Pim van der Harst, Murielle Bochud, Marc Maillard, Michel Burnier, Thomas Hedner, Sverre Kjeldsen, Björn Wahlstrand, Marketa Sjögren, Cristiano Fava, Martina Montagnana, Elisa Danese, Ole Torffvit, Bo Hedblad, Harold Snieder, John M C Connell, Morris Brown, Nilesh J Samani, Martin Farrall, Giancarlo Cesana, Giuseppe Mancia, Stefano Signorini, Guido Grassi, Susana Eyheramendy, H Erich Wichmann, Maris Laan, David P Strachan, Peter Sever, Denis Colm Shields, Alice Stanton, Peter Vollenweider, Alexander Teumer, Henry Völzke, Rainer Rettig, Christopher Newton-Cheh, Pankaj Arora, Feng Zhang, Nicole Soranzo, Timothy D Spector, Gavin Lucas, Sekar Kathiresan, David S Siscovick, Jian'an Luan, Ruth J F Loos, Nicholas J Wareham, Brenda W Penninx, Ilja M Nolte, Martin McBride, William H Miller, Stuart A Nicklin, Andrew H Baker, Delyth Graham, Robert A McDonald, Jill P Pell, Naveed Sattar, Paul Welsh, Global BPgen Consortium, Patricia Munroe, Mark J Caulfield, Alberto Zanchetti, Anna F Dominiczak

    Diterbitkan 2010-10-01
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