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pamidronate and Hypophosphatemia, Familial

pamidronate 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 Excerpts

ExcerptRelevanceReference
"To clarify the relations between reflex sympathetic dystrophy syndrome and moderate phosphate diabetes, we prospectively determined urinary phosphate excretion parameters (clearance, renal tubular reabsorption of phosphate and threshold of tubular reabsorption of phosphate) in 37 patients with reflex sympathetic dystrophy syndrome before and after treatment with 60 mg of pamidronate (n = 23) and in 35 age- and sex-matched controls."7.69Phosphate excretion in reflex sympathetic dystrophy syndrome before and after a single infusion of pamidronate. ( Cantagrel, A; Laroche, M; Mazieres, B; Moulinier, L; Redon-Dumolard, A, 1997)
"To clarify the relations between reflex sympathetic dystrophy syndrome and moderate phosphate diabetes, we prospectively determined urinary phosphate excretion parameters (clearance, renal tubular reabsorption of phosphate and threshold of tubular reabsorption of phosphate) in 37 patients with reflex sympathetic dystrophy syndrome before and after treatment with 60 mg of pamidronate (n = 23) and in 35 age- and sex-matched controls."3.69Phosphate excretion in reflex sympathetic dystrophy syndrome before and after a single infusion of pamidronate. ( Cantagrel, A; Laroche, M; Mazieres, B; Moulinier, L; Redon-Dumolard, A, 1997)
"McCune-Albright syndrome (MAS) is sometimes complicated by hypophosphatemia and abnormally low levels of 1,25(OH)(2)D in the presence of hypophosphatemia."1.33The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune-Albright syndrome. ( Imanishi, Y; Inaba, M; Jüppner, H; Kinoshita, E; Koshiyama, H; Miyauchi, A; Nakagomi, Y; Nishizawa, Y; Ozono, K; Satomura, K; Shimizu, N; Yamamoto, T, 2005)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Yamamoto, T1
Imanishi, Y1
Kinoshita, E1
Nakagomi, Y1
Shimizu, N1
Miyauchi, A1
Satomura, K1
Koshiyama, H1
Inaba, M1
Nishizawa, Y1
Jüppner, H1
Ozono, K1
Laroche, M1
Redon-Dumolard, A1
Moulinier, L1
Cantagrel, A1
Mazieres, B1

Other Studies

2 other studies available for pamidronate and Hypophosphatemia, Familial

ArticleYear
The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune-Albright syndrome.
    Journal of bone and mineral metabolism, 2005, Volume: 23, Issue:3

    Topics: Adolescent; Adult; Calcium; Child; Diphosphonates; Female; Fibroblast Growth Factor-23; Fibroblast G

2005
Phosphate excretion in reflex sympathetic dystrophy syndrome before and after a single infusion of pamidronate.
    Revue du rhumatisme (English ed.), 1997, Volume: 64, Issue:3

    Topics: Adult; Aged; Calcitriol; Calcium; Creatinine; Diphosphonates; Female; Humans; Hypophosphatemia, Fami

1997