Page last updated: 2024-11-06

thymidine and Hypophosphatemia, Familial

thymidine has been researched along with Hypophosphatemia, Familial in 2 studies

Hypophosphatemia, Familial: An inherited condition of abnormally low serum levels of PHOSPHATES (below 1 mg/liter) which can occur in a number of genetic diseases with defective reabsorption of inorganic phosphorus by the PROXIMAL RENAL TUBULES. This leads to phosphaturia, HYPOPHOSPHATEMIA, and disturbances of cellular and organ functions such as those in X-LINKED HYPOPHOSPHATEMIC RICKETS; OSTEOMALACIA; and FANCONI SYNDROME.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Takeda, E2
Yokota, I1
Ito, M1
Kobashi, H2
Saijo, T2
Kuroda, Y2
Toshima, K1
Naito, E1
Iwakuni, Y1
Miyao, M1

Other Studies

2 other studies available for thymidine and Hypophosphatemia, Familial

ArticleYear
25-Hydroxyvitamin D-24-hydroxylase in phytohemagglutinin-stimulated lymphocytes: intermediate bioresponse to 1,25-dihydroxyvitamin D3 of cells from parents of patients with vitamin D-dependent rickets type II.
    The Journal of clinical endocrinology and metabolism, 1990, Volume: 70, Issue:4

    Topics: 24,25-Dihydroxyvitamin D 3; Calcitriol; Cells, Cultured; Chromatography, High Pressure Liquid; Cytoc

1990
Rapid diagnosis of vitamin D-dependent rickets type II by use of phytohemagglutinin-stimulated lymphocytes.
    Clinica chimica acta; international journal of clinical chemistry, 1986, Mar-28, Volume: 155, Issue:3

    Topics: Calcitriol; Cell Nucleus; Cytosol; Fibroblasts; Humans; Hypophosphatemia, Familial; In Vitro Techniq

1986