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Journal Abstract Search

565 related items for PubMed ID: 28012402

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  • 4. Co-inheritance of HNF1a and GCK mutations in a family with maturity-onset diabetes of the young (MODY): implications for genetic testing.
    López-Garrido MP, Herranz-Antolín S, Alija-Merillas MJ, Giralt P, Escribano J.
    Clin Endocrinol (Oxf); 2013 Sep; 79(3):342-7. PubMed ID: 23009393
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  • 6. Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families.
    Santana LS, Caetano LA, Costa-Riquetto AD, Quedas EPS, Nery M, Collett-Solberg P, Boguszewski MCS, Vendramini MF, Crisostomo LG, Floh FO, Zarabia ZI, Kohara SK, Guastapaglia L, Passone CGB, Sewaybricker LE, Jorge AAL, Teles MG.
    Clin Genet; 2017 Oct; 92(4):388-396. PubMed ID: 28170077
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  • 10. A decision algorithm to identify patients with high probability of monogenic diabetes due to HNF1A mutations.
    Szopa M, Klupa T, Kapusta M, Matejko B, Ucieklak D, Glodzik W, Zapala B, Sani CM, Hohendorff J, Malecki MT, Skupien J.
    Endocrine; 2019 Apr; 64(1):75-81. PubMed ID: 30778899
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  • 11. MODY probability calculator for GCK and HNF1A screening in a multiethnic background population.
    Tarantino RM, Abreu GM, Fonseca ACP, Kupfer R, Pereira MFC, Campos Júnior M, Zajdenverg L, Rodacki M.
    Arch Endocrinol Metab; 2020 Feb; 64(1):17-23. PubMed ID: 31576961
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  • 12. Assessment of high-sensitivity C-reactive protein levels as diagnostic discriminator of maturity-onset diabetes of the young due to HNF1A mutations.
    Owen KR, Thanabalasingham G, James TJ, Karpe F, Farmer AJ, McCarthy MI, Gloyn AL.
    Diabetes Care; 2010 Sep; 33(9):1919-24. PubMed ID: 20724646
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  • 15. Intima-media thickness and endothelial dysfunction in GCK and HNF1A-MODY patients.
    Szopa M, Osmenda G, Wilk G, Matejko B, Skupien J, Zapala B, Młynarski W, Guzik T, Malecki MT.
    Eur J Endocrinol; 2015 Mar; 172(3):277-83. PubMed ID: 25501962
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