Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Elena V. Vislobokova"'
Autor:
Aleksander A. Baranov, Tatiana T. Batysheva, Olga V. Bykova, Nato D. Vashakmadze, Elena V. Vislobokova, Alisa V. Vitebskaya, Elena A. Vishneva, Victoria Yu. Voynova, Natalia V. Zhurkova, Ekaterina Yu. Zakharova, Larisa P. Kisel'nikova, Mikhail M. Kostik, Sergey I. Kutsev, Tea V. Margieva, Leyla S. Namazova-Baranova, Svetlana V. Mikhaylova, Sergey V. Moiseev, Tatyana S. Nagornaya, Liliia R. Selimzyanova, Alla N. Semyachkina, Olga Ya. Smirnova, Marina V. Fedoseenko, Svetlana V. Pishchal'nikova
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 4, Pp 318-336 (2023)
Hypophosphatasia is rare genetic disease caused by tissue-nonspecific alkaline phosphatase deficiency due to the mutation in the ALPL gene. Disease can manifest in utero, in childhood or in adults depending on its form and severity. This article pres
Externí odkaz:
https://doaj.org/article/dd29ce8f7c954e10bb999e43b7ae4d52
Autor:
Dmitriy A. Lezhnev, Elena V. Vislobokova, Larisa P. Kiselnikova, Natalia A. Sholokhova, Margarita V. Smyslenova, Viktor P. Truten
Publikováno v:
International Journal of Biomedicine, Vol 11, Iss 1, Pp 53-57 (2021)
The purpose of the present cohort study was a quantitative assessment of the enamel, dentin, and alveolar bone mineral density (BMD) using Cone Beam Computed Tomography (CBCT) scans in patients with X-linked hypophosphatemic rickets (HLHR) and hypoph
Externí odkaz:
https://doaj.org/article/bacb266f331246d2a55075b4a1fc2397