BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 31141481)

  • 1. Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation.
    Bayramoğlu E; Şavaş Erdeve Ş; Shi Y; Keskin M; Çetinkaya S; Kurnaz E; Muratoğlu Şahin N; Aycan Z
    J Pediatr Endocrinol Metab; 2019 Jun; 32(6):647-651. PubMed ID: 31141481
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route.
    Abalı S; Tamura M; Turan S; Atay Z; Isguven P; Güran T; Haliloglu B; Baş S; Isojima T; Kitanaka S; Bereket A
    J Pediatr Endocrinol Metab; 2020 Apr; 33(4):557-562. PubMed ID: 32049653
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Successful intermittent intravenous calcium treatment via the peripheral route in a patient with hereditary vitamin D-resistant rickets and alopecia.
    Ersoy B; Kiremitci S; Isojima T; Kitanaka S
    Horm Res Paediatr; 2015; 83(1):67-72. PubMed ID: 25573344
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation.
    Faiyaz-Ul-Haque M; AlDhalaan W; AlAshwal A; Bin-Abbas BS; AlSagheir A; Alotaiby M; Rafiq Z; Zaidi SHE
    J Pediatr Endocrinol Metab; 2018 Aug; 31(8):861-868. PubMed ID: 29949513
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enteral calcium infusion used successfully as treatment for a patient with hereditary vitamin D resistant rickets (HVDRR) without alopecia: a novel mutation.
    Huang K; Malloy P; Feldman D; Pitukcheewanont P
    Gene; 2013 Jan; 512(2):554-9. PubMed ID: 23026218
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor.
    Malloy PJ; Zhou Y; Wang J; Hiort O; Feldman D
    J Bone Miner Res; 2011 Nov; 26(11):2710-8. PubMed ID: 21812032
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cinacalcet treatment experience in hereditary vitamin D resistant rickets.
    Lucas J; Badia JL; Lucas E; Remon A
    J Pediatr Endocrinol Metab; 2020 Feb; 33(2):313-318. PubMed ID: 31926093
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary vitamin D-resistant rickets presenting as alopecia.
    Casey G; McPherson T; Kini U; Ryan F; Taibjee SM; Moss C; Burge S
    Pediatr Dermatol; 2014; 31(4):519-20. PubMed ID: 24917549
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tooth Development Associated with Mutations in Hereditary Vitamin D-Resistant Rickets.
    Hanna AE; Sanjad S; Andary R; Nemer G; Ghafari JG
    JDR Clin Trans Res; 2018 Jan; 3(1):28-34. PubMed ID: 30938651
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary vitamin D resistant rickets: identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy.
    Ma NS; Malloy PJ; Pitukcheewanont P; Dreimane D; Geffner ME; Feldman D
    Bone; 2009 Oct; 45(4):743-6. PubMed ID: 19523546
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor.
    Malloy PJ; Wang J; Srivastava T; Feldman D
    Mol Genet Metab; 2010 Jan; 99(1):72-9. PubMed ID: 19815438
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets.
    Malloy PJ; Tasic V; Taha D; Tütüncüler F; Ying GS; Yin LK; Wang J; Feldman D
    Mol Genet Metab; 2014 Jan; 111(1):33-40. PubMed ID: 24246681
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel compound heterozygous mutations in the vitamin D receptor gene in a Korean girl with hereditary vitamin D resistant rickets.
    Song JK; Yoon KS; Shim KS; Bae CW
    J Korean Med Sci; 2011 Aug; 26(8):1111-4. PubMed ID: 21860566
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Compound heterozygous mutations in the vitamin D receptor in a patient with hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia.
    Zhou Y; Wang J; Malloy PJ; Dolezel Z; Feldman D
    J Bone Miner Res; 2009 Apr; 24(4):643-51. PubMed ID: 19049339
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Different mechanisms of intestinal calcium absorption at different life stages: therapeutic implications and long-term responses to treatment in patients with hereditary vitamin D-resistant rickets.
    Chaturvedi D; Garabedian M; Carel JC; Léger J
    Horm Res Paediatr; 2012; 78(5-6):326-31. PubMed ID: 22965178
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review.
    Dodamani MH; Lila AR; Memon SS; Sarathi V; Arya S; Rane A; Sehemby MK; Garg R; Bhandare VV; Karlekar M; Patil VA; Kunwar A; Bandgar TR
    Calcif Tissue Int; 2023 Apr; 112(4):483-492. PubMed ID: 36705686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets.
    Ben Ameur S; Silve C; Chabchoub I; Damak F; Kamoun F; Toussaint A; Kmiha S; Sfaihi L; Maaloul I; Kamoun T; Aloulou H; Hachicha M
    Horm Res Paediatr; 2017; 87(1):23-29. PubMed ID: 28013309
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation update and long-term outcome after treatment with active vitamin D
    Chi Y; Sun J; Pang L; Jiajue R; Jiang Y; Wang O; Li M; Xing X; Hu Y; Zhou X; Meng X; Xia W
    Osteoporos Int; 2019 Feb; 30(2):481-489. PubMed ID: 30382318
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary 1,25-dihydroxyvitamin D-resistant rickets due to an opal mutation causing premature termination of the vitamin D receptor.
    Zhu W; Malloy PJ; Delvin E; Chabot G; Feldman D
    J Bone Miner Res; 1998 Feb; 13(2):259-64. PubMed ID: 9495519
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene.
    Mazen I; Ismail S; Amr K; El Gammal M; Abdel-Hamid M
    J Pediatr Endocrinol Metab; 2014 Sep; 27(9-10):873-8. PubMed ID: 24859502
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.