197 related articles for article (PubMed ID: 34561702)
1. X-linked hypophosphataemic rickets: Report of a novel PHEX mutation and cinacalcet as adjuvant therapy in the mineral metabolism control.
Cavaco D; Amaro P; Simões-Pereira J; Pereira MC
Mod Rheumatol Case Rep; 2022 Jan; 6(1):145-149. PubMed ID: 34561702
[TBL] [Abstract][Full Text] [Related]
2. A case of X-linked hypophosphatemic rickets: complications and the therapeutic use of cinacalcet.
Raeder H; Shaw N; Netelenbos C; Bjerknes R
Eur J Endocrinol; 2008 Dec; 159 Suppl 1():S101-5. PubMed ID: 18775977
[TBL] [Abstract][Full Text] [Related]
3. Cinacalcet in hyperparathyroidism secondary to X-linked hypophosphatemic rickets: case report and brief literature review.
Yavropoulou MP; Kotsa K; Gotzamani Psarrakou A; Papazisi A; Tranga T; Ventis S; Yovos JG
Hormones (Athens); 2010; 9(3):274-8. PubMed ID: 20688626
[TBL] [Abstract][Full Text] [Related]
4. A mosaic mutation of phosphate-regulating gene with homologies to endopeptidases on the X chromosome (PHEX) in X-linked hypophosphatemic rickets with mild bone phenotypes.
Asano S; Sako S; Funasaki Y; Takeshita Y; Niida Y; Takamura T
Endocr J; 2021 Sep; 68(9):1135-1141. PubMed ID: 33907069
[TBL] [Abstract][Full Text] [Related]
5. Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets.
Ichikawa S; Traxler EA; Estwick SA; Curry LR; Johnson ML; Sorenson AH; Imel EA; Econs MJ
Bone; 2008 Oct; 43(4):663-6. PubMed ID: 18625346
[TBL] [Abstract][Full Text] [Related]
6. Hypophosphatemic rickets caused by a novel PHEX gene mutation in an Indian girl.
Dayal D; Sharda S; Attri SV; Kumar R
J Pediatr Endocrinol Metab; 2014 Jul; 27(7-8):787-9. PubMed ID: 24756041
[TBL] [Abstract][Full Text] [Related]
7. Genetic analysis of three families with X-linked dominant hypophosphatemic rickets.
Lin X; Zhu Y; Luo J; Huang J
J Pediatr Endocrinol Metab; 2018 Jul; 31(7):789-797. PubMed ID: 29858904
[TBL] [Abstract][Full Text] [Related]
8. Validation of a next-generation sequencing (NGS) panel to improve the diagnosis of X-linked hypophosphataemia (XLH) and other genetic disorders of renal phosphate wasting.
Thiele S; Werner R; Stubbe A; Hiort O; Hoeppner W
Eur J Endocrinol; 2020 Nov; 183(5):497-504. PubMed ID: 33107440
[TBL] [Abstract][Full Text] [Related]
9. Two De Novo Mosaic Variants Within the Same Site of PHEX Gene in a Girl with X-Linked Hypophosphatemic Rickets.
Lin Y; Zhang W; Huang X; Su L; Cai Y; Liang C; Rao M; Liu L; Zeng C
Calcif Tissue Int; 2022 Feb; 110(2):266-271. PubMed ID: 34487203
[TBL] [Abstract][Full Text] [Related]
10. Calcimimetics as an adjuvant treatment for familial hypophosphatemic rickets.
Alon US; Levy-Olomucki R; Moore WV; Stubbs J; Liu S; Quarles LD
Clin J Am Soc Nephrol; 2008 May; 3(3):658-64. PubMed ID: 18256372
[TBL] [Abstract][Full Text] [Related]
11. Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial Disease.
Nielsen SR; Hansen SG; Bistrup C; Brusgaard K; Frederiksen AL
Calcif Tissue Int; 2022 Dec; 111(6):641-645. PubMed ID: 35916905
[TBL] [Abstract][Full Text] [Related]
12. CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH).
Sui T; Yuan L; Liu H; Chen M; Deng J; Wang Y; Li Z; Lai L
Hum Mol Genet; 2016 Jul; 25(13):2661-2671. PubMed ID: 27126636
[TBL] [Abstract][Full Text] [Related]
13. Novel PHEX mutation associated with hypophosphatemic rickets.
Roetzer KM; Varga F; Zwettler E; Nawrot-Wawrzyniak K; Haller J; Forster E; Klaushofer K
Nephron Physiol; 2007; 106(1):p8-12. PubMed ID: 17406123
[TBL] [Abstract][Full Text] [Related]
14. Genotype-phenotype analysis, and assessment of the importance of the zinc-binding site in PHEX in Japanese patients with X-linked hypophosphatemic rickets using 3D structure modeling.
Ishihara Y; Ohata Y; Takeyari S; Kitaoka T; Fujiwara M; Nakano Y; Yamamoto K; Yamada C; Yamamoto K; Michigami T; Mabe H; Yamaguchi T; Matsui K; Tamada I; Namba N; Yamamoto A; Etoh J; Kawaguchi A; Kosugi R; Ozono K; Kubota T
Bone; 2021 Dec; 153():116135. PubMed ID: 34333162
[TBL] [Abstract][Full Text] [Related]
15. [Genetic and clinical analysis of X-linked hypophosphatemic rickets].
Wei LY; Gong CX; Cao BY; Li XQ; Liang XJ; Li WJ; Wu D; Liu M; Su C; Chen JJ
Zhonghua Er Ke Za Zhi; 2021 Aug; 59(8):678-683. PubMed ID: 34333921
[No Abstract] [Full Text] [Related]
16. Novel PHEX gene mutation associated with X linked hypophosphatemic rickets.
Chandran M; Chng CL; Zhao Y; Bee YM; Phua LY; Clarke BL
Nephron Physiol; 2010; 116(3):p17-21. PubMed ID: 20664300
[TBL] [Abstract][Full Text] [Related]
17. Three novel PHEX gene mutations in four Chinese families with X-linked dominant hypophosphatemic rickets.
Kang QL; Xu J; Zhang Z; He JW; Lu LS; Fu WZ; Zhang ZL
Biochem Biophys Res Commun; 2012 Jul; 423(4):793-8. PubMed ID: 22713460
[TBL] [Abstract][Full Text] [Related]
18. PHEX gene mutation in a Chinese family with six cases of X-linked hypophosphatemic rickets.
Yang L; Yang J; Huang X
J Pediatr Endocrinol Metab; 2013; 26(11-12):1179-83. PubMed ID: 23813354
[TBL] [Abstract][Full Text] [Related]
19. The contribution of a novel
Chen X; Cai C; Lun S; Ye Q; Pan W; Chen Y; Wu Y; Feng T; Su F; Ma C; Luo J; Liu M; Ma G
Front Endocrinol (Lausanne); 2023; 14():1251718. PubMed ID: 38116308
[TBL] [Abstract][Full Text] [Related]
20. PHEX 3'-UTR c.*231A>G near the polyadenylation signal is a relatively common, mild, American mutation that masquerades as sporadic or X-linked recessive hypophosphatemic rickets.
Mumm S; Huskey M; Cajic A; Wollberg V; Zhang F; Madson KL; Wenkert D; McAlister WH; Gottesman GS; Whyte MP
J Bone Miner Res; 2015 Jan; 30(1):137-43. PubMed ID: 25042154
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]