melatonin 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.
Excerpt | Relevance | Reference |
---|---|---|
"Melatonin deficiency was proposed to be present in cases of neurofibromatosis 1 and to be an operating factor in progression of spinal deformities." | 1.31 | Hypophosphatemic osteomalacia in neurofibromatosis 1: hypotheses for pathogenesis and higher incidence of spinal deformity. ( Abdel-Wanis, M; Kawahara, N, 2002) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Santamaría, R | 1 |
Díaz-Tocados, JM | 1 |
Pendón-Ruiz de Mier, MV | 1 |
Robles, A | 1 |
Salmerón-Rodríguez, MD | 1 |
Ruiz, E | 1 |
Vergara, N | 1 |
Aguilera-Tejero, E | 1 |
Raya, A | 1 |
Ortega, R | 1 |
Felsenfeld, A | 1 |
Muñoz-Castañeda, JR | 1 |
Martín-Malo, A | 1 |
Aljama, P | 1 |
Rodríguez, M | 1 |
Abdel-Wanis, M | 1 |
Kawahara, N | 1 |
2 other studies available for melatonin and Hypophosphatemia, Familial
Article | Year |
---|---|
Increased Phosphaturia Accelerates The Decline in Renal Function: A Search for Mechanisms.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Animals; Antioxidants; Cell Line; Female; Glomerular Fil | 2018 |
Hypophosphatemic osteomalacia in neurofibromatosis 1: hypotheses for pathogenesis and higher incidence of spinal deformity.
Topics: Hypophosphatemia, Familial; Incidence; Melatonin; Neurofibromatosis 1; Spine | 2002 |