BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 3796683)

  • 1. "Idiopathic" hypercalciuria and hereditary hypophosphatemic rickets. Two phenotypical expressions of a common genetic defect.
    Tieder M; Modai D; Shaked U; Samuel R; Arie R; Halabe A; Maor J; Weissgarten J; Averbukh Z; Cohen N
    N Engl J Med; 1987 Jan; 316(3):125-9. PubMed ID: 3796683
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary hypophosphatemic rickets with hypercalciuria.
    Tieder M; Modai D; Samuel R; Arie R; Halabe A; Bab I; Gabizon D; Liberman UA
    N Engl J Med; 1985 Mar; 312(10):611-7. PubMed ID: 2983203
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Osteomalacia in hereditary hypophosphatemic rickets with hypercalciuria: a correlative clinical-histomorphometric study.
    Gazit D; Tieder M; Liberman UA; Passi-Even L; Bab IA
    J Clin Endocrinol Metab; 1991 Jan; 72(1):229-35. PubMed ID: 1986023
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hypophosphatemic rickets accompanying congenital microvillous atrophy.
    Kagitani K; Yamamoto T; Miki K; Matsumoto S; Shima M; Tajiri H; Harada T; Okada S
    J Bone Miner Res; 1998 Dec; 13(12):1946-52. PubMed ID: 9844114
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: implications for correct diagnosis and treatment.
    Tieder M; Arie R; Bab I; Maor J; Liberman UA
    Nephron; 1992; 62(2):176-81. PubMed ID: 1436310
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary hypophosphatemic rickets with hypercalciuria: case report.
    Areses-Trapote R; López-García JA; Ubetagoyena-Arrieta M; Eizaguirre A; Sáez-Villaverde R
    Nefrologia; 2012 Jul; 32(4):529-34. PubMed ID: 22806288
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hypercalciuria secondary to chronic hypophosphatemia.
    Navarro JF; Teruel JL; Montalban C; Gallego N; Ortuño J
    Miner Electrolyte Metab; 1994; 20(5):255-8. PubMed ID: 7700212
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypercalciuric hypophosphatemic rickets, mineral balance, bone histomorphometry, and therapeutic implications of hypercalciuria.
    Chen C; Carpenter T; Steg N; Baron R; Anast C
    Pediatrics; 1989 Aug; 84(2):276-80. PubMed ID: 2787497
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Updates on rickets and osteomalacia: the role of NaPi-2c/SLC34A3 and hypophosphataemic rickets].
    Segawa H; Shiozaki Y; Minoshima S; Miyamoto K
    Clin Calcium; 2013 Oct; 23(10):1445-50. PubMed ID: 24076642
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Long-term influence of calcitriol (1,25-dihydroxyvitamin D) and supplemental phosphate in X-linked hypophosphatemic rickets.
    Chesney RW; Mazess RB; Rose P; Hamstra AJ; DeLuca HF; Breed AL
    Pediatrics; 1983 Apr; 71(4):559-67. PubMed ID: 6300745
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Healing of bone disease in X-linked hypophosphatemic rickets/osteomalacia. Induction and maintenance with phosphorus and calcitriol.
    Harrell RM; Lyles KW; Harrelson JM; Friedman NE; Drezner MK
    J Clin Invest; 1985 Jun; 75(6):1858-68. PubMed ID: 3839245
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Serum 1,25-dihydroxyvitamin D levels in normal subjects and in patients with hereditary rickets or bone disease.
    Scriver CR; Reade TM; DeLuca HF; Hamstra AJ
    N Engl J Med; 1978 Nov; 299(18):976-9. PubMed ID: 308618
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary hypophosphatemic rickets with hypercalciuria: pathophysiology, clinical presentation, diagnosis and therapy.
    Bergwitz C; Miyamoto KI
    Pflugers Arch; 2019 Jan; 471(1):149-163. PubMed ID: 30109410
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis.
    Bergwitz C; Roslin NM; Tieder M; Loredo-Osti JC; Bastepe M; Abu-Zahra H; Frappier D; Burkett K; Carpenter TO; Anderson D; Garabedian M; Sermet I; Fujiwara TM; Morgan K; Tenenhouse HS; Juppner H
    Am J Hum Genet; 2006 Feb; 78(2):179-92. PubMed ID: 16358214
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria.
    Ichikawa S; Sorenson AH; Imel EA; Friedman NE; Gertner JM; Econs MJ
    J Clin Endocrinol Metab; 2006 Oct; 91(10):4022-7. PubMed ID: 16849419
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune-Albright syndrome.
    Yamamoto T; Imanishi Y; Kinoshita E; Nakagomi Y; Shimizu N; Miyauchi A; Satomura K; Koshiyama H; Inaba M; Nishizawa Y; Jüppner H; Ozono K
    J Bone Miner Metab; 2005; 23(3):231-7. PubMed ID: 15838626
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary hypophosphatemic rickets with hypercalciuria: a study for the phosphate transporter gene type IIc and osteoblastic function.
    Yamamoto T; Michigami T; Aranami F; Segawa H; Yoh K; Nakajima S; Miyamoto K; Ozono K
    J Bone Miner Metab; 2007; 25(6):407-13. PubMed ID: 17968493
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review.
    Dodamani MH; Memon SS; Karlekar M; Lila AR; Khan M; Sarathi V; Arya S; Jamale T; Thakare S; Patil VA; Shah NS; Bergwitz C; Bandgar TR
    Calcif Tissue Int; 2024 Feb; 114(2):137-146. PubMed ID: 37981601
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene.
    Jones AO; Tzenova J; Frappier D; Crumley MJ; Roslin NM; Kos CH; Tieder M; Langman CB; Proesmans W; Carpenter TO; Rice A; Anderson D; Morgan K; Fujiwara TM; Tenenhouse HS
    J Am Soc Nephrol; 2001 Mar; 12(3):507-514. PubMed ID: 11181798
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A compound heterozygous mutation in SLC34A3 causes hereditary hypophosphatemic rickets with hypercalciuria in a Chinese patient.
    Chi Y; Zhao Z; He X; Sun Y; Jiang Y; Li M; Wang O; Xing X; Sun AY; Zhou X; Meng X; Xia W
    Bone; 2014 Feb; 59():114-21. PubMed ID: 24246249
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.