Osobennosti metabolizma kostnoy tkanipri sindrome mnozhestvennykh endokrinnykhneoplaziy 1 tipa

Autor: Rozhinskaya L Ya, Kirdyankina N O, Mokrysheva N G, Tyul'pakov A N, Vorontsov A, Rostomyan L G

Publikováno v: Ожирение и метаболизм, Vol 6, Iss 4, Pp 42-46 (2009)

Bone metabolism and changes in bone mineral density (BMD) are very important in patients with multiple endocrine neoplasia (MEN) type 1 syndrome. Case report: we present a clinical case of primary hyperparathyroidism (PHPT) in a patient with a famila

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46bb17aa92234a0007b34f08b9054372
https://www.omet-endojournals.ru/jour/article/view/4878

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[TYPE 1 MULTIPLE ENDOCRINE NEOPLASIA SYNDROME AND FAMILIAL ISOLATED HYPERPARATHYROIDISM].

Autor: Mamedova EO, Pigarova EA, Mokrysheva NG, Kuznetsov SN, Kim IV, Kuznetsov NS, Rozhinskaya LY, Tyul'pakov AN

Publikováno v: Klinicheskaia meditsina [Klin Med (Mosk)] 2015; Vol. 93 (11), pp. 73-7.

[Clinical and molecular genetic verification of Frasers syndrome, false male hermaphroditism and chronic glomerulonephritis (the first description in Russia)].

Autor: Novikova EO; Endocrinology Research Centre., Rubtsov PM; Engelhardt Institute of Molecular Biology of the Russian Academy of Sciences., Sverdlova PS; Engelhardt Institute of Molecular Biology of the Russian Academy of Sciences., Tyul'pakov AN; Endocrinology Research Centre.

Publikováno v: Problemy endokrinologii [Probl Endokrinol (Mosk)] 2009 Apr 15; Vol. 55 (2), pp. 51-53. Date of Electronic Publication: 2009 Apr 15.