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Autor:
S. S. Rodionova, A. I. Snetkov, A. D. Akinshina, I. V. Bulycheva, A. N. Torgashin, T. A. Grebennikova, Zh. E. Belaya, Е. M. Agafonova, N. V. Toroptsova, O. A. Nikitinskaya
Publikováno v:
Научно-практическая ревматология, Vol 57, Iss 6, Pp 708-712 (2019)
Tumor-induced hypophosphatemic osteomalacia is a rare disease and its diagnosis presents certain difficulties. This is primarily due to small tumor size and to the absence of local clinical symptoms. Adult-onset newly diagnosed hypophosphatemia concu
Externí odkaz:
https://doaj.org/article/76e817c0e90e40e293169d3236594388