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 *

113 related articles for article (PubMed ID: 2506251)

  • 1. Ultrasound demonstration of nephrocalcinosis in William's syndrome.
    Jantarasami T; Larew M; Kao SC; Smith W
    J Clin Ultrasound; 1989 Sep; 17(7):533-4. PubMed ID: 2506251
    [No Abstract]   [Full Text] [Related]  

  • 2. Uncommon cribfellows: an infant with hypercalcemia, nephrocalcinosis, and acidosis: Answers.
    Ehlayel AM; Copelovitch L
    Pediatr Nephrol; 2018 Oct; 33(10):1697-1699. PubMed ID: 29460158
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With Nephrocalcinosis.
    Jobst-Schwan T; Pannes A; Schlingmann KP; Eckardt KU; Beck BB; Wiesener MS
    Kidney Blood Press Res; 2015; 40(5):443-51. PubMed ID: 26304832
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Idiopathic Infantile Hypercalcemia, Presenting in Adulthood--No Longer Idiopathic Nor Infantile: Two Case Reports and Review.
    Tray KA; Laut J; Saidi A
    Conn Med; 2015; 79(10):593-7. PubMed ID: 26731879
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nephrocalcinosis in Bartter's syndrome. Demonstration by ultrasonography.
    Cumming WA; Ohlsson A
    Pediatr Radiol; 1984; 14(2):125-6. PubMed ID: 6728537
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Uncommon cribfellows: an infant with hypercalcemia, nephrocalcinosis, and acidosis: Questions.
    Ehlayel AM; Copelovitch L
    Pediatr Nephrol; 2018 Oct; 33(10):1695. PubMed ID: 29460157
    [No Abstract]   [Full Text] [Related]  

  • 8. SHORT syndrome in a two-year-old girl - case report.
    Klatka M; Rysz I; Kozyra K; Polak A; Kołłątaj W
    Ital J Pediatr; 2017 May; 43(1):44. PubMed ID: 28472977
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel SLC12A1 gene mutation associated with hyperparathyroidism, hypercalcemia, nephrogenic diabetes insipidus, and nephrocalcinosis in four patients.
    Wongsaengsak S; Vidmar AP; Addala A; Kamil ES; Sequeira P; Fass B; Pitukcheewanont P
    Bone; 2017 Apr; 97():121-125. PubMed ID: 28095294
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A New Homozygous IGF1R Variant Defines a Clinically Recognizable Incomplete Dominant form of SHORT Syndrome.
    Prontera P; Micale L; Verrotti A; Napolioni V; Stangoni G; Merla G
    Hum Mutat; 2015 Nov; 36(11):1043-7. PubMed ID: 26252249
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ultrasound demonstration of diffuse cortical nephrocalcinosis in a case of primary hyperoxaluria.
    Wilson DA; Wenzl JE; Altshuler GP
    AJR Am J Roentgenol; 1979 Apr; 132(4):659-61. PubMed ID: 106704
    [No Abstract]   [Full Text] [Related]  

  • 12. [William's syndrome: a phenotypic diagnosis].
    Moreno R; Lacassie Y
    Rev Chil Pediatr; 1982; 53(2):156-61. PubMed ID: 7178565
    [No Abstract]   [Full Text] [Related]  

  • 13. Increased renal medullary echogenicity in patients with Williams syndrome.
    Cote G; Jequier S; Kaplan P
    Pediatr Radiol; 1989; 19(6-7):481-3. PubMed ID: 2671904
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gray-scale ultrasonic demonstration of nephrocalcinosis.
    Cacciarelli AA; Young N; Levine AJ
    Radiology; 1978 Aug; 128(2):459-60. PubMed ID: 663260
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Echocardiographic and Doppler findings in the Williams syndrome.
    Brand A; Keren A; Reifen RM; Gross-Kieselstein E; Armir N
    Am J Cardiol; 1989 Mar; 63(9):633-5. PubMed ID: 2645763
    [No Abstract]   [Full Text] [Related]  

  • 16. Ultrasound diagnosis of nephrocalcinosis in preterm infants.
    Woolfield N; Haslam R; Le Quesne G; Chambers HM; Hogg R; Jureidini K
    Arch Dis Child; 1988 Jan; 63(1):86-8. PubMed ID: 3279919
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome.
    Baştuğ F; Nalçacıoğlu H; Baş VN; Tekatlı-Çelik B; Çetinkaya H; Yel S
    Turk J Pediatr; 2018; 60(2):210-215. PubMed ID: 30325132
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in PIK3R1 can lead to APDS2, SHORT syndrome or a combination of the two.
    Bravo García-Morato M; García-Miñaúr S; Molina Garicano J; Santos Simarro F; Del Pino Molina L; López-Granados E; Ferreira Cerdán A; Rodríguez Pena R
    Clin Immunol; 2017 Jun; 179():77-80. PubMed ID: 28302518
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Nephrocalcinosis: sonographic detection in Cushing syndrome.
    Foley LC; Luisiri A; Graviss ER; Campbell JB
    AJR Am J Roentgenol; 1982 Sep; 139(3):610-2. PubMed ID: 6981334
    [No Abstract]   [Full Text] [Related]  

  • 20. EXPANSION OF THE SHORT SYNDROME PHENOTYPE IN AN ADULT PATIENT WITH UNILATERAL BASAL GANGLIA CALCIFICATION.
    Salinas-Torres VM; De La O-Expinoza EA; Salinas-Torres RA
    Genet Couns; 2016; 27(4):479-483. PubMed ID: 30226966
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.