Novel GLIS3 mutation in patient with neonatal diabetes mellitus and congenital hypothyroidism (NDH-syndrome) by Yu. V. Tikhonovich, L. G. Chernich, I. N. Velikanov, V. M. Polyakova, E. V. Vasilyev, V. M. Petrov, E. V. Shreder, Е. V. Glavatskich, A. N. Tyulpakov

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VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW by I. I. Larina, N. M. Platonova, E. A. Troshina, A. A. Roslyakova, D. G. Belzevich, L. S. Selivanova, M. Yu. Ukina, L. V. Nikankina, N. M. Malysheva, A. N. Tyulpakov, L. D. Kovalevich

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Clinical, hormonal and molecular-genetic characteristics of monogenic diabetes mellitus associated with the mutations in the <i>INS</i> gene by Yu. V. Tikhonovich, E. E. Petryaykina, A. V. Timofeev, N. A. Zubkova, A. A. Kolodkina, E. L. Sorkina, E. V. Vasiliev, V. M. Petrov, E. A. Andrianova, L. I. Zilberman, G. N. Svetlova, A. L. Кalinin, P. M. Rubtsov, S. L. Кiselev, A. V. Panova, E. V. Shreder, T. S. Krasnova, B. P. Kulieva, I. V. Gariaeva, I. G. Rybkina, O. A. Malievskiy, A. N. Tyulpakov

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