120 related articles for article (PubMed ID: 21414629)
1. Mild infantile hypercalcemia: diagnostic tests and outcomes.
Koltin D; Rachmiel M; Wong BY; Cole DE; Harvey E; Sochett E
J Pediatr; 2011 Aug; 159(2):215-21.e1. PubMed ID: 21414629
[TBL] [Abstract][Full Text] [Related]
2. Idiopathic infantile hypercalcemia: rapid response to treatment with calcitonin.
Alon U; Berkowitz D; Berant M
Child Nephrol Urol; 1992; 12(1):47-50. PubMed ID: 1606583
[TBL] [Abstract][Full Text] [Related]
3. Linear growth in relation to the circulating concentrations of insulin-like growth factor I, parathyroid hormone, and 25-hydroxy vitamin D in children with nutritional rickets before and after treatment: endocrine adaptation to vitamin D deficiency.
Soliman AT; Al Khalaf F; Alhemaidi N; Al Ali M; Al Zyoud M; Yakoot K
Metabolism; 2008 Jan; 57(1):95-102. PubMed ID: 18078865
[TBL] [Abstract][Full Text] [Related]
4. Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic Findings.
Lenherr-Taube N; Young EJ; Furman M; Elia Y; Assor E; Chitayat D; Uster T; Kirwin S; Robbins K; Vinette KMB; Daneman A; Marshall CR; Collins C; Thummel K; Sochett E; Levine MA
J Clin Endocrinol Metab; 2021 Sep; 106(10):2915-2937. PubMed ID: 34125233
[TBL] [Abstract][Full Text] [Related]
5. [Familial hypocalciuric hypercalcemia: a new mutation].
Ubetagoyena Arrieta M; Castaño González L; Pérez de Nanclares Leal G; Arruebarrena Lizarraga D; Imaz Murguiondo M; Areses Trapote R
An Pediatr (Barc); 2011 Jan; 74(1):47-50. PubMed ID: 21185797
[TBL] [Abstract][Full Text] [Related]
6. Hypocalciuric hypercalcemia presenting as neonatal rib fractures: a newly described mutation of the calcium-sensing receptor gene.
Nyweide K; Feldman KW; Gunther DF; Done S; Lewis C; Van Eenwyk C
Pediatr Emerg Care; 2006 Nov; 22(11):722-4. PubMed ID: 17110864
[TBL] [Abstract][Full Text] [Related]
7. [Hypocalciuric hypercalcemia due to de novo mutation of the calcium sensing receptor].
Sarli M; Fradinger E; Zanchetta J
Medicina (B Aires); 2004; 64(4):337-9. PubMed ID: 15338977
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Prenatal hyperechogenic kidneys in three cases of infantile hypercalcemia associated with SLC34A1 mutations.
Hureaux M; Molin A; Jay N; Saliou AH; Spaggiari E; Salomon R; Benachi A; Vargas-Poussou R; Heidet L
Pediatr Nephrol; 2018 Oct; 33(10):1723-1729. PubMed ID: 29959532
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Mild Idiopathic Infantile Hypercalcemia-Part 2: A Longitudinal Observational Study.
Lenherr-Taube N; Furman M; Assor E; Elia Y; Collins C; Thummel K; Levine MA; Sochett E
J Clin Endocrinol Metab; 2021 Sep; 106(10):2938-2948. PubMed ID: 34139759
[TBL] [Abstract][Full Text] [Related]
12. Childhood Sustained Hypercalcemia: A Diagnostic Challenge.
Çullas İlarslan NE; Şıklar Z; Berberoğlu M
J Clin Res Pediatr Endocrinol; 2017 Dec; 9(4):315-322. PubMed ID: 28443817
[TBL] [Abstract][Full Text] [Related]
13. Skeletal consequences of familial hypocalciuric hypercalcaemia vs. primary hyperparathyroidism.
Christensen SE; Nissen PH; Vestergaard P; Heickendorff L; Rejnmark L; Brixen K; Mosekilde L
Clin Endocrinol (Oxf); 2009 Dec; 71(6):798-807. PubMed ID: 19250271
[TBL] [Abstract][Full Text] [Related]
14. A novel mutation (L174R) in the Ca2+-sensing receptor gene associated with familial hypocalciuric hypercalcemia.
Ward BK; Stuckey BG; Gutteridge DH; Laing NG; Pullan PT; Ratajczak T
Hum Mutat; 1997; 10(3):233-5. PubMed ID: 9298824
[No Abstract] [Full Text] [Related]
15. Familial hypocalciuric hypercalcemia caused by an R648stop mutation in the calcium-sensing receptor gene.
Yamauchi M; Sugimoto T; Yamaguchi T; Yano S; Wang J; Bai M; Brown EM; Chihara K
J Bone Miner Res; 2002 Dec; 17(12):2174-82. PubMed ID: 12469911
[TBL] [Abstract][Full Text] [Related]
16. Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey.
Raue F; Pichl J; Dörr HG; Schnabel D; Heidemann P; Hammersen G; Jaursch-Hancke C; Santen R; Schöfl C; Wabitsch M; Haag C; Schulze E; Frank-Raue K
Clin Endocrinol (Oxf); 2011 Dec; 75(6):760-5. PubMed ID: 21645025
[TBL] [Abstract][Full Text] [Related]
17. Self-limited neonatal familial hyperparathyroidism associated with hypercalciuria and renal tubular acidosis in three siblings.
Nishiyama S; Tomoeda S; Inoue F; Ohta T; Matsuda I
Pediatrics; 1990 Sep; 86(3):421-7. PubMed ID: 2167460
[TBL] [Abstract][Full Text] [Related]
18. Clinical evaluation of calcium metabolism in adult T-cell leukemia/lymphoma.
Fukumoto S; Matsumoto T; Ikeda K; Yamashita T; Watanabe T; Yamaguchi K; Kiyokawa T; Takatsuki K; Shibuya N; Ogata E
Arch Intern Med; 1988 Apr; 148(4):921-5. PubMed ID: 2895617
[TBL] [Abstract][Full Text] [Related]
19. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor.
Pearce SH; Williamson C; Kifor O; Bai M; Coulthard MG; Davies M; Lewis-Barned N; McCredie D; Powell H; Kendall-Taylor P; Brown EM; Thakker RV
N Engl J Med; 1996 Oct; 335(15):1115-22. PubMed ID: 8813042
[TBL] [Abstract][Full Text] [Related]
20. Increased cardiovascular mortality and normalized serum calcium in patients with mild hypercalcemia followed up for 25 years.
Lundgren E; Lind L; Palmér M; Jakobsson S; Ljunghall S; Rastad J
Surgery; 2001 Dec; 130(6):978-85. PubMed ID: 11742326
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
