These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 33329754)

  • 1. Molecular Analysis of
    Zou M; Guven A; BinEssa HA; Al-Rijjal RA; Meyer BF; Alzahrani AS; Shi Y
    Front Genet; 2020; 11():607517. PubMed ID: 33329754
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A.
    Demir K; Kattan WE; Zou M; Durmaz E; BinEssa H; Nalbantoğlu Ö; Al-Rijjal RA; Meyer B; Özkan B; Shi Y
    PLoS One; 2015; 10(7):e0131376. PubMed ID: 26132292
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and genetic analysis of patients with vitamin D-dependent rickets type 1A.
    Durmaz E; Zou M; Al-Rijjal RA; Bircan I; Akçurin S; Meyer B; Shi Y
    Clin Endocrinol (Oxf); 2012 Sep; 77(3):363-9. PubMed ID: 22443290
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I.
    Tahir S; Demirbilek H; Ozbek MN; Baran RT; Tanriverdi S; Hussain K
    Horm Res Paediatr; 2016; 85(5):309-17. PubMed ID: 26982175
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A.
    Dursun F; Özgürhan G; Kırmızıbekmez H; Keskin E; Hacıhamdioğlu B
    J Clin Res Pediatr Endocrinol; 2019 Feb; 11(1):34-40. PubMed ID: 30282619
    [TBL] [Abstract][Full Text] [Related]  

  • 6. NOVEL
    Demir K; Zou M; Al-Rijjal RA; BinEssa H; Acar S; Durmaz E; Çatlı G; Al-Enezi AF; Alzahrani AS; Meyer BF; Shi Y
    Endocr Pract; 2020 Jan; 26(1):72-81. PubMed ID: 31557081
    [No Abstract]   [Full Text] [Related]  

  • 7. Vitamin D 1alpha-hydroxylase gene mutations in patients with 1alpha-hydroxylase deficiency.
    Kim CJ; Kaplan LE; Perwad F; Huang N; Sharma A; Choi Y; Miller WL; Portale AA
    J Clin Endocrinol Metab; 2007 Aug; 92(8):3177-82. PubMed ID: 17488797
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel CYP27B1 mutation causes a feline vitamin D-dependent rickets type IA.
    Grahn RA; Ellis MR; Grahn JC; Lyons LA
    J Feline Med Surg; 2012 Aug; 14(8):587-90. PubMed ID: 22553308
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A.
    Hu WW; Ke YH; He JW; Fu WZ; Wang C; Zhang H; Yue H; Gu JM; Zhang ZL
    J Pediatr Endocrinol Metab; 2014 Mar; 27(3-4):335-41. PubMed ID: 24197768
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel pathogenic mutation of the CYP27B1 gene in a patient with vitamin D-dependent rickets type 1: a case report.
    Babiker AM; Al Gadi I; Al-Jurayyan NA; Al Nemri AM; Al Haboob AA; Al Boukai AA; Al Zahrani A; Habib HA
    BMC Res Notes; 2014 Nov; 7():783. PubMed ID: 25371233
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Long-term clinical outcome and the identification of homozygous
    Cho JH; Kang E; Kim GH; Lee BH; Choi JH; Yoo HW
    Ann Pediatr Endocrinol Metab; 2016 Sep; 21(3):169-173. PubMed ID: 27777911
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genetics and clinical manifestations of patients with vitamin D dependent rickets type 1A.
    Ozden A; Doneray H
    J Pediatr Endocrinol Metab; 2021 Jun; 34(6):781-789. PubMed ID: 33823104
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical spectrum and diagnostic challenges of vitamin D dependent rickets type 1A (VDDR1A) caused by
    Aftab S; Khan SA; Malik MI; Imran A; Anjum MN; Saeed A; Qureshi AA; Cheema HA
    J Pediatr Endocrinol Metab; 2023 Feb; 36(2):152-157. PubMed ID: 36524979
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel mutation in hereditary vitamin D resistant rickets causing exon skipping.
    Hawa NS; Cockerill FJ; Vadher S; Hewison M; Rut AR; Pike JW; O'Riordan JL; Farrow SM
    Clin Endocrinol (Oxf); 1996 Jul; 45(1):85-92. PubMed ID: 8796143
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Novel mutations in the 1alpha-hydroxylase (P450c1) gene in three families with pseudovitamin D-deficiency rickets resulting in loss of functional enzyme activity in blood-derived macrophages.
    Smith SJ; Rucka AK; Berry JL; Davies M; Mylchreest S; Paterson CR; Heath DA; Tassabehji M; Read AP; Mee AP; Mawer EB
    J Bone Miner Res; 1999 May; 14(5):730-9. PubMed ID: 10320521
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CYP2R1 mutations causing vitamin D-deficiency rickets.
    Thacher TD; Levine MA
    J Steroid Biochem Mol Biol; 2017 Oct; 173():333-336. PubMed ID: 27473561
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel Homozygous CYP27B1 Gene Mutation in Vitamin D-Dependent Rickets Type 1A (VDDR1A) Disorder: A Case Report.
    Al Homyani DK; Alhemaiani SK
    Front Endocrinol (Lausanne); 2022; 13():862022. PubMed ID: 35663328
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel G102E mutation of CYP27B1 in a large family with vitamin D-dependent rickets type 1.
    Alzahrani AS; Zou M; Baitei EY; Alshaikh OM; Al-Rijjal RA; Meyer BF; Shi Y
    J Clin Endocrinol Metab; 2010 Sep; 95(9):4176-83. PubMed ID: 20534770
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel Compound Heterozygous Mutations in the CYP27B1 Gene Lead to Pseudovitamin D-Deficient Rickets.
    Koek WN; Zillikens MC; van der Eerden BC; van Leeuwen JP
    Calcif Tissue Int; 2016 Sep; 99(3):326-31. PubMed ID: 27364341
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.