BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 24386581)

  • 21. 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]  

  • 22. The functional response to furosemide in a case of de Toni-Debre-Fanconi disease.
    Santos-Atherton D; Frenk S
    Acta Endocrinol Suppl (Copenh); 1986; 279():452-7. PubMed ID: 3022525
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Autosomal Dominant Hypophosphatemic Rickets Presenting in a Phenotypically Normal Adult Female.
    Mualla H; Bae SA; Yaqub A
    Case Rep Endocrinol; 2019; 2019():8917519. PubMed ID: 30949368
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Refractory rickets due to Fanconi's Syndrome secondary to Wilson's disease.
    Selvan C; Thukral A; Chakraborthy PP; Bhattacharya R; Roy A; Goswani S; Meher D; Ghosh S; Mukhopadhyay S; Chowdhury S
    Indian J Endocrinol Metab; 2012 Dec; 16(Suppl 2):S399-401. PubMed ID: 23565442
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Different forms of clinical presentation of an autosomal dominant hypophosphatemic rickets caused by a FGF23 mutation in one family].
    Negri AL; Negrotti T; Alonso G; Pasqualini T
    Medicina (B Aires); 2004; 64(2):103-6. PubMed ID: 15628294
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Debré-De Toni-Fanconi syndrome with glycogenosis of the liver].
    Bauer B
    Klin Wochenschr; 1968 Mar; 46(6):317-28. PubMed ID: 5245557
    [No Abstract]   [Full Text] [Related]  

  • 27. X-Linked Hypophosphatemic Rickets: Multisystemic Disorder in Children Requiring Multidisciplinary Management.
    Baroncelli GI; Mora S
    Front Endocrinol (Lausanne); 2021; 12():688309. PubMed ID: 34421819
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A bedridden young lady with hypophosphatemic rickets treated with denosumab: a case report.
    Al-Sharafi BA; Al-Yousfi NA; Bamashmus SA
    J Med Case Rep; 2021 Feb; 15(1):48. PubMed ID: 33549117
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Hypocalcaemic and hypophosphatemic rickets.
    Lambert AS; Linglart A
    Best Pract Res Clin Endocrinol Metab; 2018 Aug; 32(4):455-476. PubMed ID: 30086869
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hereditary Hypophosphatemic Rickets with Hypercalciuria (HHRH) Presenting with Genu Valgum Deformity: Treatment with Phosphate Supplementation and Surgical Correction.
    Colazo JM; Reasoner SA; Holt G; Faugere MCM; Dahir KM
    Case Rep Endocrinol; 2020; 2020():1047327. PubMed ID: 32695531
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Determination of metabolites of vitamin D in a case of Debré-De Toni-Fanconi syndrome secondary to cystinosis].
    Ottolenghi A; Colussi G; De Chiara A; Gerosa R; Gasparro C; Colacicco B
    Pediatr Med Chir; 1986; 8(2):287-90. PubMed ID: 3491362
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phosphate matters when investigating hypercalcemia: a mutation in SLC34A3 causing HHRH.
    Tang AR; Hinz LE; Khan A; Kline GA
    Endocrinol Diabetes Metab Case Rep; 2019 Jul; 2019(1):1-6. PubMed ID: 31352694
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Evaluation of a role for 1,25-dihydroxyvitamin D3 in the pathogenesis and treatment of X-linked hypophosphatemic rickets and osteomalacia.
    Drezner MK; Lyles KW; Haussler MR; Harrelson JM
    J Clin Invest; 1980 Nov; 66(5):1020-32. PubMed ID: 6253520
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mineralized tissues in hypophosphatemic rickets.
    Robinson ME; AlQuorain H; Murshed M; Rauch F
    Pediatr Nephrol; 2020 Oct; 35(10):1843-1854. PubMed ID: 31392510
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephaly.
    Jackson CB; Bauer MF; Schaller A; Kotzaeridou U; Ferrarini A; Hahn D; Chehade H; Barbey F; Tran C; Gallati S; Haeberli A; Eggimann S; Bonafé L; Nuoffer JM
    Eur J Pediatr; 2016 Apr; 175(4):517-25. PubMed ID: 26563427
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A single case of hypophosphatemic rickets with hypercalciuria.
    Nishiyama S; Inoue F; Matsuda I
    J Pediatr Gastroenterol Nutr; 1986; 5(5):826-9. PubMed ID: 3761117
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Plasma intact fibroblast growth factor 23 level is a useful tool for diagnostic approach of renal hypophosphatemia.
    Giralt M; Chocron S; Ferrer R; Ariceta G
    Pediatr Nephrol; 2021 Apr; 36(4):1025-1028. PubMed ID: 33492457
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hypophosphatemic Rickets with R179W Mutation in FGFR23 Gene - A Rare But Treatable Cause of Refractory Rickets.
    Sandal S; Arora V; Verma IC
    Indian J Pediatr; 2021 Jan; 88(1):61-63. PubMed ID: 32415663
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Homozygous ectonucleotide pyrophosphatase/phosphodiesterase 1 variants in a girl with hypophosphatemic rickets and literature review].
    Liu ZQ; Chen XB; Song FY; Gao K; Qiu MF; Qian Y; Du M
    Zhonghua Er Ke Za Zhi; 2017 Nov; 55(11):858-861. PubMed ID: 29141319
    [No Abstract]   [Full Text] [Related]  

  • 40. Phosphatonins: From Discovery to Therapeutics.
    Kritmetapak K; Kumar R
    Endocr Pract; 2023 Jan; 29(1):69-79. PubMed ID: 36210014
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.