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 *

161 related articles for article (PubMed ID: 31751313)

  • 1. Intractable hypercalcaemia during pregnancy and the postpartum secondary to pathogenic variants in CYP24A1.
    Arnold N; O'Toole V; Huynh T; Smith HC; Luxford C; Clifton-Bligh R; Eastman CJ
    Endocrinol Diabetes Metab Case Rep; 2019 Nov; 2019():. PubMed ID: 31751313
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Persistent hypercalcaemia associated with two pathogenic variants in the
    Leszczyńska D; Szatko A; Latocha J; Kochman M; Duchnowska M; Wójcicka A; Misiorowski W; Zgliczyníski W; Glinicki P
    Front Endocrinol (Lausanne); 2024; 15():1355916. PubMed ID: 38665259
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hypervitaminosis D Secondary to a
    Collins L; Boehm E; Luxford C; Clifton-Bligh R; Grill V
    JBMR Plus; 2023 Sep; 7(9):e10788. PubMed ID: 37701149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Young Woman With Recurrent Gestational Hypercalcemia and Acute Pancreatitis Caused by CYP24A1 Deficiency.
    Woods GN; Saitman A; Gao H; Clarke NJ; Fitzgerald RL; Chi NW
    J Bone Miner Res; 2016 Oct; 31(10):1841-1844. PubMed ID: 27105398
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [CYP24A1 gene defect manifesting with gestational hypercalcemia].
    Györkös A; Tőke J; Sohár G; Kovács M; Goldfinger J; Vajda G; Kalmár T; Tóth M
    Orv Hetil; 2022 Jul; 163(31):1237-1242. PubMed ID: 35908214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Biallelic CYP24A1 variants presenting during pregnancy: clinical and biochemical phenotypes.
    Griffin TP; Joyce CM; Alkanderi S; Blake LM; O'Keeffe DT; Bogdanet D; Islam MN; Dennedy MC; Gillan JE; Morrison JJ; O'Brien T; Sayer JA; Bell M; O'Shea PM
    Endocr Connect; 2020 Jun; 9(6):530-541. PubMed ID: 32375123
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failure.
    Colussi G; Ganon L; Penco S; De Ferrari ME; Ravera F; Querques M; Primignani P; Holtzman EJ; Dinour D
    Nephrol Dial Transplant; 2014 Mar; 29(3):636-43. PubMed ID: 24235083
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Myositis, rhabdomyolysis and severe hypercalcaemia in a body builder.
    Ravindran R; Witczak J; Bahl S; Premawardhana LDKE; Adlan M
    Endocrinol Diabetes Metab Case Rep; 2020 Jul; 2020():. PubMed ID: 32698126
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypercalcemia and CYP24A1 Gene Mutation Diagnosed in the 2nd Trimester of a Twin Pregnancy: A Case Report.
    Romašovs A; Jaunozola L; Berga-Švītiņa E; Daneberga Z; Miklaševičs E; Pīrāgs V
    Am J Case Rep; 2021 Oct; 22():e931116. PubMed ID: 34662328
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two cases of spontaneous remission of primary hyperparathyroidism due to auto-infarction: different management and their outcomes.
    Novodvorsky P; Hussein Z; Arshad MF; Iqbal A; Fernando M; Munir A; Balasubramanian SP
    Endocrinol Diabetes Metab Case Rep; 2019 May; 2019():. PubMed ID: 31063971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Management of primary hyperparathyroidism in pregnancy: a case series.
    McCarthy A; Howarth S; Khoo S; Hale J; Oddy S; Halsall D; Fish B; Mariathasan S; Andrews K; Oyibo SO; Samyraju M; Gajewska-Knapik K; Park SM; Wood D; Moran C; Casey RT
    Endocrinol Diabetes Metab Case Rep; 2019 May; 2019():. PubMed ID: 31096181
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Kidney function and influence of sunlight exposure in patients with impaired 24-hydroxylation of vitamin D due to CYP24A1 mutations.
    Figueres ML; Linglart A; Bienaime F; Allain-Launay E; Roussey-Kessler G; Ryckewaert A; Kottler ML; Hourmant M
    Am J Kidney Dis; 2015 Jan; 65(1):122-6. PubMed ID: 25446019
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Loss-of-function mutations of CYP24A1, the vitamin D 24-hydroxylase gene, cause long-standing hypercalciuric nephrolithiasis and nephrocalcinosis.
    Dinour D; Beckerman P; Ganon L; Tordjman K; Eisenstein Z; Holtzman EJ
    J Urol; 2013 Aug; 190(2):552-7. PubMed ID: 23470222
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CYP24A1 loss of function: Clinical phenotype of monoallelic and biallelic mutations.
    Carpenter TO
    J Steroid Biochem Mol Biol; 2017 Oct; 173():337-340. PubMed ID: 28093352
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Calcium and bone homeostasis in heterozygous carriers of CYP24A1 mutations: A cross-sectional study.
    Cools M; Goemaere S; Baetens D; Raes A; Desloovere A; Kaufman JM; De Schepper J; Jans I; Vanderschueren D; Billen J; De Baere E; Fiers T; Bouillon R
    Bone; 2015 Dec; 81():89-96. PubMed ID: 26117226
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of Nephrolithiasis.
    Nesterova G; Malicdan MC; Yasuda K; Sakaki T; Vilboux T; Ciccone C; Horst R; Huang Y; Golas G; Introne W; Huizing M; Adams D; Boerkoel CF; Collins MT; Gahl WA
    Clin J Am Soc Nephrol; 2013 Apr; 8(4):649-57. PubMed ID: 23293122
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Case report: Two heterozygous pathogenic variants of CYP24A1: A novel cause of hypercalcemia and nephrocalcinosis in adulthood.
    Brunerova L; Remes O; Zoubkova V; Votypka P
    Front Med (Lausanne); 2022; 9():1020096. PubMed ID: 36703897
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gestational hypercalcemia: Prevalence and biochemical profile.
    Schoenmakers I; Piec I; Baban S; Bärebring L; Green D; Washbourne CJ; Tang JCY; Fraser WD; Augustin H
    J Steroid Biochem Mol Biol; 2020 May; 199():105611. PubMed ID: 32007562
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternal Hypercalcemia Due to Failure of 1,25-Dihydroxyvitamin-D3 Catabolism in a Patient With CYP24A1 Mutations.
    Shah AD; Hsiao EC; O'Donnell B; Salmeen K; Nussbaum R; Krebs M; Baumgartner-Parzer S; Kaufmann M; Jones G; Bikle DD; Wang Y; Mathew AS; Shoback D; Block-Kurbisch I
    J Clin Endocrinol Metab; 2015 Aug; 100(8):2832-6. PubMed ID: 26097993
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Milk-alkali syndrome: a 'quick ease' or a 'long-lasting problem'.
    Wang M; Cho C; Gray C; Chai TY; Daud R; Luttrell M
    Endocrinol Diabetes Metab Case Rep; 2020 May; 2020():. PubMed ID: 32408269
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.