BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

320 related articles for article (PubMed ID: 29753922)

  • 1. Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe.
    Barisic I; Boban L; Akhmedzhanova D; Bergman JEH; Cavero-Carbonell C; Grinfelde I; Materna-Kiryluk A; Latos-Bieleńska A; Randrianaivo H; Zymak-Zakutnya N; Sansovic I; Lanzoni M; Morris JK
    Eur J Med Genet; 2018 Sep; 61(9):499-507. PubMed ID: 29753922
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Beckwith-Wiedemann syndrome: What do you search in prenatal diagnosis? About 14 cases].
    Le Vaillant C; Beneteau C; Chan-Leconte N; David A; Riteau AS
    Gynecol Obstet Fertil; 2015 Nov; 43(11):705-11. PubMed ID: 26542939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies.
    Wilkins-Haug L; Porter A; Hawley P; Benson CB
    Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):58-62. PubMed ID: 19107956
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal sonographic diagnosis of Beckwith-Wiedemann syndrome in association with a single umbilical artery.
    Hamada H; Fujiki Y; Obata-Yasuoka M; Watanabe H; Yamada N; Kubo T
    J Clin Ultrasound; 2001; 29(9):535-8. PubMed ID: 11745867
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Prenatal diagnosis of Beckwith-Wiedemann syndrome in third trimester].
    Włoch A; Czuba B; Borowski D; Włoch S; Wojciechowska E; Wielgos M; Sodowski K
    Ginekol Pol; 2006 Feb; 77(2):103-9. PubMed ID: 16736967
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Intrauterine growth and ultrasound findings in fetuses with Beckwith-Wiedemann syndrome.
    Ranzini AC; Day-Salvatore D; Turner T; Smulian JC; Vintzileos AM
    Obstet Gynecol; 1997 Apr; 89(4):538-42. PubMed ID: 9083309
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fetal intracardiac rhabdomyoma in beckwith-wiedemann syndrome.
    Longardt AC; Nonnenmacher A; Graul-Neumann L; Opgen-Rhein B; Henrich W; Bührer C; Hüseman D
    J Clin Ultrasound; 2014; 42(9):569-73. PubMed ID: 24752985
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Wiedemann-Beckwith syndrome: clinical and epidemiological analysis of a consecutive series of cases in Spain].
    Arroyo Carrera I; Martínez-Frías ML; Egüés Jimeno J; García Martínez MJ; Eloína Cimadevilla Sánchez C; Bermejo Sánchez E
    An Esp Pediatr; 1999 Feb; 50(2):161-5. PubMed ID: 10199027
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984-2007.
    Boyle B; McConkey R; Garne E; Loane M; Addor MC; Bakker MK; Boyd PA; Gatt M; Greenlees R; Haeusler M; Klungsøyr K; Latos-Bielenska A; Lelong N; McDonnell R; Métneki J; Mullaney C; Nelen V; O'Mahony M; Pierini A; Rankin J; Rissmann A; Tucker D; Wellesley D; Dolk H
    BJOG; 2013 May; 120(6):707-16. PubMed ID: 23384325
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of Beckwith-Wiedemann syndrome.
    Williams DH; Gauthier DW; Maizels M
    Prenat Diagn; 2005 Oct; 25(10):879-84. PubMed ID: 16193463
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.
    Colvin J; Bower C; Dickinson JE; Sokol J
    Pediatrics; 2005 Sep; 116(3):e356-63. PubMed ID: 16140678
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of severe structural congenital malformations in Europe.
    Garne E; Loane M; Dolk H; De Vigan C; Scarano G; Tucker D; Stoll C; Gener B; Pierini A; Nelen V; Rösch C; Gillerot Y; Feijoo M; Tincheva R; Queisser-Luft A; Addor MC; Mosquera C; Gatt M; Barisic I
    Ultrasound Obstet Gynecol; 2005 Jan; 25(1):6-11. PubMed ID: 15619321
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions.
    Pedersen RN; Calzolari E; Husby S; Garne E;
    Arch Dis Child; 2012 Mar; 97(3):227-32. PubMed ID: 22247246
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith-Wiedemann syndrome.
    Abbasi N; Moore A; Chiu P; Ryan G; Weksberg R; Shuman C; Steele L; Chitayat D
    Prenat Diagn; 2021 Jun; 41(7):798-816. PubMed ID: 33687072
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Prevalence of selected congenital anomalies in the Czech Republic: renal and cardiac anomalies and congenital chromosomal aberrations].
    Šípek A; Gregor V; Horáček J; Šípek A; Langhammer P
    Epidemiol Mikrobiol Imunol; 2013 Sep; 62(3):112-28. PubMed ID: 24116699
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The prenatal diagnosis of Beckwith-Wiedemann syndrome using ultrasound and magnetic resonance imaging.
    Storm DW; Hirselj DA; Rink B; O'Shaughnessy R; Alpert SA
    Urology; 2011 Jan; 77(1):208-10. PubMed ID: 20573391
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal detection of a congenital pancreatic cyst and Beckwith-Wiedemann syndrome.
    Fremond B; Poulain P; Odent S; Milon J; Treguier C; Babut JM
    Prenat Diagn; 1997 Mar; 17(3):276-80. PubMed ID: 9110373
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal imaging throughout gestation in Beckwith-Wiedemann syndrome.
    Shieh HF; Estroff JA; Barnewolt CE; Zurakowski D; Tan WH; Buchmiller TL
    Prenat Diagn; 2019 Aug; 39(9):792-795. PubMed ID: 30784096
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epidemiology of orofacial clefts in a Danish county over 35 years - Before and after implementation of a prenatal screening programme for congenital anomalies.
    Paaske EB; Garne E
    Eur J Med Genet; 2018 Sep; 61(9):489-492. PubMed ID: 29753919
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Holt Oram syndrome: a registry-based study in Europe.
    Barisic I; Boban L; Greenlees R; Garne E; Wellesley D; Calzolari E; Addor MC; Arriola L; Bergman JE; Braz P; Budd JL; Gatt M; Haeusler M; Khoshnood B; Klungsoyr K; McDonnell B; Nelen V; Pierini A; Queisser-Wahrendorf A; Rankin J; Rissmann A; Rounding C; Tucker D; Verellen-Dumoulin C; Dolk H
    Orphanet J Rare Dis; 2014 Oct; 9():156. PubMed ID: 25344219
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.