155 related articles for article (PubMed ID: 37908980)
1. Vitamin D Hydroxylation-deficient Rickets Type 1A Misdiagnosed as Normocalcemic Primary Hyperparathyroidism.
Rivero-García P; Aguilar-Lugo-Gerez JJ; Kimball TN; Reza-Albarrán AA
JCEM Case Rep; 2023 Jul; 1(4):luad084. PubMed ID: 37908980
[TBL] [Abstract][Full Text] [Related]
2. A case of vitamin D hydroxylation-deficient rickets type 1A caused by 2 novel pathogenic variants in CYP27B1 gene.
Kim YM; Jang YY; Jeong JE; Park HJ; Jang JH; Kim JK
Ann Pediatr Endocrinol Metab; 2019 Jun; 24(2):137-141. PubMed ID: 31261480
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 1alpha(OH)D3 One-alpha-hydroxy-cholecalciferol--an active vitamin D analog. Clinical studies on prophylaxis and treatment of secondary hyperparathyroidism in uremic patients on chronic dialysis.
Brandi L
Dan Med Bull; 2008 Nov; 55(4):186-210. PubMed ID: 19232159
[TBL] [Abstract][Full Text] [Related]
5. Calcitonin is a major regulator for the expression of renal 25-hydroxyvitamin D3-1alpha-hydroxylase gene in normocalcemic rats.
Shinki T; Ueno Y; DeLuca HF; Suda T
Proc Natl Acad Sci U S A; 1999 Jul; 96(14):8253-8. PubMed ID: 10393981
[TBL] [Abstract][Full Text] [Related]
6. 1α,24(S)(OH)2D2 normalizes bone morphology and serum parathyroid hormone without hypercalcemia in 25-hydroxyvitamin D-1-hydroxylase (CYP27B1)-deficient mice, an animal model of vitamin D deficiency with secondary hyperparathyroidism.
St-Arnaud R; Arabian A; Yu VW; Akhouayri O; Knutson JC; Strugnell SA
J Endocrinol Invest; 2008 Aug; 31(8):711-7. PubMed ID: 18852532
[TBL] [Abstract][Full Text] [Related]
7. Targeted ablation of the 25-hydroxyvitamin D 1alpha -hydroxylase enzyme: evidence for skeletal, reproductive, and immune dysfunction.
Panda DK; Miao D; Tremblay ML; Sirois J; Farookhi R; Hendy GN; Goltzman D
Proc Natl Acad Sci U S A; 2001 Jun; 98(13):7498-503. PubMed ID: 11416220
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Correction of the abnormal mineral ion homeostasis with a high-calcium, high-phosphorus, high-lactose diet rescues the PDDR phenotype of mice deficient for the 25-hydroxyvitamin D-1alpha-hydroxylase (CYP27B1).
Dardenne O; Prud'homme J; Hacking SA; Glorieux FH; St-Arnaud R
Bone; 2003 Apr; 32(4):332-40. PubMed ID: 12689675
[TBL] [Abstract][Full Text] [Related]
10. Rescue of the pseudo-vitamin D deficiency rickets phenotype of CYP27B1-deficient mice by treatment with 1,25-dihydroxyvitamin D3: biochemical, histomorphometric, and biomechanical analyses.
Dardenne O; Prudhomme J; Hacking SA; Glorieux FH; St-Arnaud R
J Bone Miner Res; 2003 Apr; 18(4):637-43. PubMed ID: 12674324
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Vitamin D dependent rickets type I.
Kim CJ
Korean J Pediatr; 2011 Feb; 54(2):51-4. PubMed ID: 21503197
[TBL] [Abstract][Full Text] [Related]
14. Genetic disorders of Vitamin D biosynthesis and degradation.
Miller WL
J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):101-108. PubMed ID: 27060335
[TBL] [Abstract][Full Text] [Related]
15. Vitamin D deficiency or resistance and hypophosphatemia.
Sarathi V; Dhananjaya MS; Karlekar M; Lila AR
Best Pract Res Clin Endocrinol Metab; 2024 Mar; 38(2):101876. PubMed ID: 38365463
[TBL] [Abstract][Full Text] [Related]
16. [Primary hyperparathyroidism. Postoperative normocalcemic hyperparathyrinemia after curative parathyroidectomy].
Hermann M
Chirurg; 2010 May; 81(5):447-53. PubMed ID: 19468699
[TBL] [Abstract][Full Text] [Related]
17. Targeted inactivation of the 25-hydroxyvitamin D(3)-1(alpha)-hydroxylase gene (CYP27B1) creates an animal model of pseudovitamin D-deficiency rickets.
Dardenne O; Prud'homme J; Arabian A; Glorieux FH; St-Arnaud R
Endocrinology; 2001 Jul; 142(7):3135-41. PubMed ID: 11416036
[TBL] [Abstract][Full Text] [Related]
18. Vitamin D-Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?
Molin A; Wiedemann A; Demers N; Kaufmann M; Do Cao J; Mainard L; Dousset B; Journeau P; Abeguile G; Coudray N; Mittre H; Richard N; Weryha G; Sorlin A; Jones G; Kottler ML; Feillet F
J Bone Miner Res; 2017 Sep; 32(9):1893-1899. PubMed ID: 28548312
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
