Hasil Pencarian - Nadia Tinto

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  1. 1
    Cystic Fibrosis-Related Diabetes (CFRD): Overview of Associated Genetic Factors

    Cystic Fibrosis-Related Diabetes (CFRD): Overview of Associated Genetic Factors oleh Fernanda Iafusco, Giovanna Maione, Francesco Maria Rosanio, Enza Mozzillo, Adriana Franzese, Nadia Tinto

    Diterbitkan 2021-03-01
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  2. 2
    High Frequency of Haplotype HLA-DQ7 in Celiac Disease Patients from South Italy: Retrospective Evaluation of 5,535 Subjects at Risk of Celiac Disease.

    High Frequency of Haplotype HLA-DQ7 in Celiac Disease Patients from South Italy: Retrospective Evaluation of 5,535 Subjects at Risk of Celiac Disease. oleh Nadia Tinto, Arturo Cola, Chiara Piscopo, Marina Capuano, Martina Galatola, Luigi Greco, Lucia Sacchetti

    Diterbitkan 2015-01-01
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  3. 3
    The Pathogenic Diagnosis in Pediatric Diabetology: Next Generation Sequencing and Precision Therapy

    The Pathogenic Diagnosis in Pediatric Diabetology: Next Generation Sequencing and Precision Therapy oleh Giovanna Maione, Fernanda Iafusco, Angela Zanfardino, Alessia Piscopo, Gulsum Ozen, Dario Iafusco, Nadia Tinto

    Diterbitkan 2023-02-01
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  4. 4
    NGS Analysis Revealed Digenic Heterozygous <i>GCK</i> and <i>HNF1A</i> Variants in a Child with Mild Hyperglycemia: A Case Report

    NGS Analysis Revealed Digenic Heterozygous <i>GCK</i> and <i>HNF1A</i> Variants in a Child with Mild Hyperglycemia: A Case Report oleh Fernanda Iafusco, Giovanna Maione, Cristina Mazzaccara, Francesca Di Candia, Enza Mozzillo, Adriana Franzese, Nadia Tinto

    Diterbitkan 2021-06-01
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  5. 5
    Molecular Epidemiology of Mitochondrial Cardiomyopathy: A Search Among Mitochondrial and Nuclear Genes

    Molecular Epidemiology of Mitochondrial Cardiomyopathy: A Search Among Mitochondrial and Nuclear Genes oleh Cristina Mazzaccara, Bruno Mirra, Ferdinando Barretta, Martina Caiazza, Barbara Lombardo, Olga Scudiero, Nadia Tinto, Giuseppe Limongelli, Giulia Frisso

    Diterbitkan 2021-05-01
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  6. 6
    The Hidden Fragility in the Heart of the Athletes: A Review of Genetic Biomarkers

    The Hidden Fragility in the Heart of the Athletes: A Review of Genetic Biomarkers oleh Ferdinando Barretta, Bruno Mirra, Emanuele Monda, Martina Caiazza, Barbara Lombardo, Nadia Tinto, Olga Scudiero, Giulia Frisso, Cristina Mazzaccara

    Diterbitkan 2020-09-01
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  7. 7
    Analysis of Corneal Deformation in Paediatric Patients Affected by Maturity Onset Diabetes of the Young Type 2

    Analysis of Corneal Deformation in Paediatric Patients Affected by Maturity Onset Diabetes of the Young Type 2 oleh Michele Lanza, Enza Mozzillo, Rosa Boccia, Ludovica Fedi, Francesca Di Candia, Nadia Tinto, Paolo Melillo, Francesca Simonelli, Adriana Franzese

    Diterbitkan 2023-04-01
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  8. 8
    Correction: MicroRNA-449a Overexpression, Reduced NOTCH1 Signals and Scarce Goblet Cells Characterize the Small Intestine of Celiac Patients.

    Correction: MicroRNA-449a Overexpression, Reduced NOTCH1 Signals and Scarce Goblet Cells Characterize the Small Intestine of Celiac Patients. oleh Marina Capuano, Laura Iaffaldano, Nadia Tinto, Donatella Montanaro, Valentina Capobianco, Valentina Izzo, Francesca Tucci, Giancarlo Troncone, Luigi Greco, Lucia Sacchetti

    Diterbitkan 2012-01-01
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  9. 9
    MicroRNA-449a overexpression, reduced NOTCH1 signals and scarce goblet cells characterize the small intestine of celiac patients.

    MicroRNA-449a overexpression, reduced NOTCH1 signals and scarce goblet cells characterize the small intestine of celiac patients. oleh Marina Capuano, Laura Iaffaldano, Nadia Tinto, Donatella Montanaro, Valentina Capobianco, Valentina Izzo, Francesca Tucci, Giancarlo Troncone, Luigi Greco, Lucia Sacchetti

    Diterbitkan 2011-01-01
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  10. 10
    Glucokinase gene mutations: structural and genotype-phenotype analyses in MODY children from South Italy.

    Glucokinase gene mutations: structural and genotype-phenotype analyses in MODY children from South Italy. oleh Nadia Tinto, Adriana Zagari, Marina Capuano, Alfonso De Simone, Valentina Capobianco, Gerardo Daniele, Michela Giugliano, Raffaella Spadaro, Adriana Franzese, Lucia Sacchetti

    Diterbitkan 2008-01-01
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  11. 11
    Improving the estimation of celiac disease sibling risk by non-HLA genes.

    Improving the estimation of celiac disease sibling risk by non-HLA genes. oleh Valentina Izzo, Michele Pinelli, Nadia Tinto, Maria Valeria Esposito, Arturo Cola, Maria Pia Sperandeo, Francesca Tucci, Sergio Cocozza, Luigi Greco, Lucia Sacchetti

    Diterbitkan 2011-01-01
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  12. 12
    Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother

    Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant a... oleh Elena Longobardi, Francesco Miceli, Agnese Secondo, Rita Cicatiello, Antonella Izzo, Nadia Tinto, Sebastien Moutton, Frédéric Tran Mau-Them, Antonio Vitobello, Maurizio Taglialatela

    Diterbitkan 2021-05-01
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  13. 13
    The Association of Autoimmune Diseases with Type 1 Diabetes Mellitus in Children Depends Also by the Length of Partial Clinical Remission Phase (Honeymoon)

    The Association of Autoimmune Diseases with Type 1 Diabetes Mellitus in Children Depends Also by the Length of Partial Clinical Remission Phase (Honeymoon) oleh Gulsum Ozen, Angela Zanfardino, Santino Confetto, Alessia Piscopo, Francesca Casaburo, Nadia Tinto, Fernanda Iafusco, Gulsah Ozen, Emanuele Miraglia del Giudice, Medine Aysin Tasar, Arzu Yilmaz, Dario Iafusco

    Diterbitkan 2020-01-01
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  14. 14
    Glucokinase (GCK) mutations and their characterization in MODY2 children of southern Italy.

    Glucokinase (GCK) mutations and their characterization in MODY2 children of southern Italy. oleh Marina Capuano, Carmen Maria Garcia-Herrero, Nadia Tinto, Carla Carluccio, Valentina Capobianco, Iolanda Coto, Arturo Cola, Dario Iafusco, Adriana Franzese, Adriana Zagari, Maria Angeles Navas, Lucia Sacchetti

    Diterbitkan 2012-01-01
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  15. 15
    An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment

    An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment oleh Francesca Di Candia, Valentina Di Iorio, Nadia Tinto, Riccardo Bonfanti, Claudio Iovino, Francesco Maria Rosanio, Ludovica Fedi, Fernanda Iafusco, Francesca Arrigoni, Rita Malesci, Francesca Simonelli, Andrea Rigamonti, Adriana Franzese, Enza Mozzillo

    Diterbitkan 2023-11-01
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  16. 16
    Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF).

    Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF). oleh Michele Pinelli, Fabio Acquaviva, Fabrizio Barbetti, Elisabetta Caredda, Sergio Cocozza, Maurizio Delvecchio, Enza Mozzillo, Daniele Pirozzi, Francesco Prisco, Ivana Rabbone, Lucia Sacchetti, Nadia Tinto, Sonia Toni, Stefano Zucchini, Dario Iafusco, Italian Study Group on Diabetes of the Italian Society of Pediatric Endocrinology and Diabetology

    Diterbitkan 2013-01-01
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