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المؤلفون: Maria Teresa Pallotta, Eleonora Panfili, Maria Laura Belladonna, Eva Tirelli, Giada Mondanelli, Carmine Vacca, Francesca Fallarino, Alberta Iacono, Elisa Proietti, Elena Orecchini, Paolo Prontera, Susanna Esposito, Ciriana Orabona, Marco Gargaro, Giulio Frontino, Ursula Grohmann, Paolo Puccetti
المصدر: Human Molecular Genetics
مصطلحات موضوعية: Proband, AcademicSubjects/SCI01140, endocrine system diseases, Wolfram syndrome, medicine.medical_treatment, Inflammation, Biology, medicine.disease_cause, Systemic inflammation, 03 medical and health sciences, Exon, 0302 clinical medicine, Genetics, medicine, Humans, Child, Molecular Biology, Genetics (clinical), 030304 developmental biology, Dominance (genetics), 0303 health sciences, Mutation, nutritional and metabolic diseases, Membrane Proteins, Wolfram Syndrome, General Medicine, Sequence Analysis, DNA, medicine.disease, Cytokine, Gene Expression Regulation, 030220 oncology & carcinogenesis, Immunology, Leukocytes, Mononuclear, Cytokines, Female, General Article, medicine.symptom
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe0b316008de70e613afd7e6ec3223f8Test
https://pubmed.ncbi.nlm.nih.gov/33693650Test -
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المؤلفون: Vilma Mantovani, Alessandro Salina, Sabrina Giglio, Maurizio Delvecchio, Stefano Tumini, Lorenzo Iughetti, Sonia Toni, Fabrizio Barbetti, Giulio Frontino, Valeria Grasso, Valentino Cherubini, Enza Mozzillo, Patrizia Ippolita Patera, Rosa Di Paola, Giulio Maltoni, Marco Marigliano, Giovanna Contreas, Ivana Rabbone, Nadia Tinto, Giuseppe d'Annunzio, Vittoria Cauvin, Dario Iafusco, Giuseppina Salzano
المساهمون: Delvecchio, Maurizio, Mozzillo, Enza, Salzano, Giuseppina, Iafusco, Dario, Frontino, Giulio, Patera, Patrizia I, Rabbone, Ivana, Cherubini, Valentino, Grasso, Valeria, Tinto, Nadia, Giglio, Sabrina, Contreas, Giovanna, Di Paola, Rosa, Salina, Alessandro, Cauvin, Vittoria, Tumini, Stefano, D'Annunzio, Giuseppe, Iughetti, Lorenzo, Mantovani, Vilma, Maltoni, Giulio, Toni, Sonia, Marigliano, Marco, Barbetti, Fabrizio
المصدر: The Journal of Clinical Endocrinology & Metabolism. 102:1826-1834
مصطلحات موضوعية: Male, Potassium Channels, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Type 2 diabetes, Biochemistry, Germinal Center Kinases, 0302 clinical medicine, Endocrinology, Neonatal diabetes mellitus, Hepatocyte Nuclear Factor 1-alpha, 030212 general & internal medicine, Child, Diabetes, Protein-Serine-Threonine Kinases, Prognosis, Adolescent, Autoantibodies, Child, Preschool, Diabetes Complications, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Female, Hepatocyte Nuclear Factor 4, Humans, Infant, Infant, Newborn, Italy, Potassium Channels, Inwardly Rectifying, Retrospective Studies, Biochemistry (medical), Inwardly Rectifying, HNF1A, Diabetes, neonatal diabetes, neonatal diabetes, Type 2, Type 1, medicine.medical_specialty, Genetic counseling, 030209 endocrinology & metabolism, Protein Serine-Threonine Kinases, Non autoimmune diabetes, Maturity onset diabetes of the young, 03 medical and health sciences, Internal medicine, Diabetes mellitus, Diabetes Mellitus, medicine, Preschool, Type 1 diabetes, Clical-Diagnosis, Young Mody, Children, Mutations, Adolescentis, Prevalence, Type-2, Hyperglycemia, Complications, Epidemiology, business.industry, Newborn, medicine.disease, Impaired fasting glucose, Settore MED/03 - Genetica Medica, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7685536f47b63116edbafb7e2d3c1c68Test
https://doi.org/10.1210/jc.2016-2490Test