phosphorus has been researched along with Genetic Diseases, X-Chromosome Linked in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (46.15) | 29.6817 |
| 2010's | 7 (53.85) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Boot, AM; Carpenter, TO; Chen, CY; Högler, W; Imel, EA; Kakkis, E; Linglart, A; Mao, M; Padidela, R; Portale, AA; San Martin, J; Skrinar, A; Van't Hoff, W; Whyte, MP | 1 |
| Attri, SV; Dayal, D; Kumar, R; Sharda, S | 1 |
| Avondo, S; Evola, FR; Gioitta Iachino, S; Pavone, V; Sessa, G; Testa, G | 1 |
| Yasuda, T | 1 |
| Choucair, MK; Nabbout, LA; Salti, IS | 1 |
| Carpenter, TO; DiMeglio, LA; Econs, MJ; Hui, SL; Imel, EA | 1 |
| Dietz, W; Kjellberg, H; Lundgren, T; Norén, JG; Rizell, S | 1 |
| Ozono, K | 1 |
| Carpenter, TO; Gundberg, CM; Insogna, KL; Liu, ES; Simpson, CA | 1 |
| Damiani, D; de Castro, LC; de Menezes Filho, H | 1 |
| Clemens, TL; Drezner, MK; Feng, JQ; Kumar, R; Rowe, PS; Takaiwa, M; Xie, Y; Yuan, B | 1 |
| Baum, M; Seikaly, MG; Waber, PG | 1 |
| Endo, I; Fukumoto, S; Inoue, D; Matsumoto, T; Michigami, T; Minagawa, M; Namba, N; Ozono, K; Sugimoto, T; Tanaka, H; Yamauchi, M | 1 |
4 review(s) available for phosphorus and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Hypophosphatemic rickets: etiology, clinical features and treatment.
Topics: Bone and Bones; Familial Hypophosphatemic Rickets; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Gene Expression Regulation; Genetic Diseases, X-Linked; Humans; Mutation; PHEX Phosphate Regulating Neutral Endopeptidase; Phosphorus | 2015 |
[Rickets].
Topics: Animals; Calcitriol; Child; Cholecalciferol; Extracellular Matrix Proteins; Familial Hypophosphatemic Rickets; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Genetic Diseases, X-Linked; Glycoproteins; Humans; Osteocytes; PHEX Phosphate Regulating Neutral Endopeptidase; Phosphoproteins; Phosphorus; Vitamin D Deficiency | 2009 |
[Bone and joint diseases in children. Phosphaturic hormone, FGF23, and bone metabolism].
Topics: Bone and Bones; Child; Familial Hypophosphatemic Rickets; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Genetic Diseases, X-Linked; Humans; Hypophosphatemia; Hypophosphatemia, Familial; Osteomalacia; Phosphorus; Receptors, Fibroblast Growth Factor | 2010 |
Hypophosphatemic rickets and osteomalacia.
Topics: Adolescent; Child; Familial Hypophosphatemic Rickets; Fibroblast Growth Factor-23; Genetic Diseases, X-Linked; Humans; Infant; Osteomalacia; Phosphorus | 2006 |
3 trial(s) available for phosphorus and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Burosumab Therapy in Children with X-Linked Hypophosphatemia.
Topics: Alkaline Phosphatase; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Child; Child, Preschool; Familial Hypophosphatemic Rickets; Female; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Genetic Diseases, X-Linked; Growth; Humans; Kidney Tubules; Knee Joint; Male; Pain Management; Phosphorus; Radiography; Severity of Illness Index | 2018 |
Treatment of X-linked hypophosphatemia with calcitriol and phosphate increases circulating fibroblast growth factor 23 concentrations.
Topics: Adolescent; Adult; Calcitriol; Calcium Channel Agonists; Child; Child, Preschool; Cohort Studies; Familial Hypophosphatemic Rickets; Female; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Follow-Up Studies; Genetic Diseases, X-Linked; Humans; Infant; Phosphates; Phosphorus; Prospective Studies | 2010 |
Urinary prostaglandins and the effect of indomethacin on phosphate excretion in children with hypophosphatemic rickets.
Topics: Adolescent; Anti-Inflammatory Agents, Non-Steroidal; Child; Child, Preschool; Creatinine; Cross-Over Studies; Dinoprostone; Double-Blind Method; Familial Hypophosphatemic Rickets; Female; Genetic Diseases, X-Linked; Humans; Indomethacin; Male; Phosphates; Phosphorus; Prospective Studies; Prostaglandins | 2008 |
6 other study(ies) available for phosphorus and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Hypophosphatemic rickets caused by a novel PHEX gene mutation in an Indian girl.
Topics: Amino Acid Sequence; Amino Acid Substitution; Calcitriol; Child, Preschool; Familial Hypophosphatemic Rickets; Female; Genetic Diseases, X-Linked; Humans; India; PHEX Phosphate Regulating Neutral Endopeptidase; Phosphates; Phosphorus; White People | 2014 |
An unusual case of autonomous hyperparathyroidism in a patient with X-linked hypophosphatemic rickets and Kallmann syndrome.
Topics: Adolescent; Alkaline Phosphatase; Calcium; Familial Hypophosphatemic Rickets; Genetic Diseases, X-Linked; Humans; Hyperparathyroidism, Secondary; Kallmann Syndrome; Male; Parathyroid Hormone; Phosphates; Phosphorus; Time Factors | 2009 |
Altered inorganic composition of dental enamel and dentin in primary teeth from girls with Turner syndrome.
Topics: Amelogenesis; Calcium; Carbon; Chromosomes, Human, X; Dental Enamel; Dentin; Dentinogenesis; Electron Probe Microanalysis; Female; Genetic Diseases, X-Linked; Humans; Karyotyping; Knowledge Bases; Microradiography; Microscopy, Electron, Scanning; Microscopy, Polarization; Minerals; Oxygen; Phosphorus; Tooth Calcification; Tooth, Deciduous; Turner Syndrome | 2010 |
Calcitonin administration in X-linked hypophosphatemia.
Topics: Calcitonin; Case-Control Studies; Dihydroxycholecalciferols; Familial Hypophosphatemic Rickets; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Genetic Diseases, X-Linked; Humans; Phosphorus | 2011 |
Aberrant Phex function in osteoblasts and osteocytes alone underlies murine X-linked hypophosphatemia.
Topics: Animals; Biological Transport; Bone and Bones; Disease Models, Animal; Familial Hypophosphatemic Rickets; Femur; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Genetic Diseases, X-Linked; Kidney; Mice; Mice, Knockout; Osteoblasts; Osteocytes; PHEX Phosphate Regulating Neutral Endopeptidase; Phosphorus; Radiography; Vitamin D | 2008 |
Clinical usefulness of measurement of fibroblast growth factor 23 (FGF23) in hypophosphatemic patients: proposal of diagnostic criteria using FGF23 measurement.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Child; Child, Preschool; Cross-Sectional Studies; Familial Hypophosphatemic Rickets; Female; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Genetic Diseases, X-Linked; Humans; Hypophosphatemia; Infant; Male; Middle Aged; Osteomalacia; Phosphorus | 2008 |