BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 18216702)

  • 1. Isolated facial hemihyperplasia: manifestation of Beckwith-Wiedemann syndrome.
    Sathienkijkanchai A; Prucka SK; Grant JH; Robin NH
    J Craniofac Surg; 2008 Jan; 19(1):279-83. PubMed ID: 18216702
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Malignant melanoma and Wiedemann-Beckwith syndrome in childhood.
    Livingstone E; Caliebe A; Egberts F; Proksch E; Buiting K; Schubert C; Claviez A; Siebert R; Hauschild A
    Klin Padiatr; 2010 Nov; 222(6):388-90. PubMed ID: 21058226
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in Iceland].
    Pálsson GI; Finnsdóttir V; Jóhannsson JH; Ingvarsson S
    Laeknabladid; 2005 Nov; 91(11):837-40. PubMed ID: 16264244
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth.
    Cohen MM
    Am J Med Genet; 1994 Aug; 52(2):233-4. PubMed ID: 7802016
    [No Abstract]   [Full Text] [Related]  

  • 5. Beckwith-Wiedemann syndrome.
    Weksberg R; Shuman C; Smith AC
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of the Beckwith-Wiedemann syndrome.
    Winter SC; Curry CJ; Smith JC; Kassel S; Miller L; Andrea J
    Am J Med Genet; 1986 May; 24(1):137-41. PubMed ID: 3518454
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case of familial isolated hemihyperplasia.
    Heilstedt HA; Bacino CA
    BMC Med Genet; 2004 Feb; 5():1. PubMed ID: 15040809
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Beckwith Wiedemann syndrome: presentation of a case report.
    Narea Matamala G; Fernández Toro Mde L; Villalabeitía Ugarte E; Landaeta Mendoza M
    Med Oral Patol Oral Cir Bucal; 2008 Oct; 13(10):E640-3. PubMed ID: 18830172
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frequency of Wiedemann-Beckwith syndrome in Germany; rate of hemihyperplasia and of tumours in affected children.
    Wiedemann HR
    Eur J Pediatr; 1997 Mar; 156(3):251. PubMed ID: 9083776
    [No Abstract]   [Full Text] [Related]  

  • 10. Recognition and management of the infant with Beckwith-Wiedemann Syndrome.
    Spivey PS; Bradshaw WT
    Adv Neonatal Care; 2009 Dec; 9(6):279-84; quiz 285. PubMed ID: 20010144
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
    Eggermann T
    Horm Res; 2009 Apr; 71 Suppl 2():30-5. PubMed ID: 19407494
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome.
    Itoh N; Becroft DM; Reeve AE; Morison IM
    Am J Med Genet; 2000 May; 92(2):111-6. PubMed ID: 10797434
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
    Enklaar T; Zabel BU; Prawitt D
    Expert Rev Mol Med; 2006 Jul; 8(17):1-19. PubMed ID: 16842655
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Beckwith-Wiedemann Syndrome (BWS): a case report and literature review.
    Ogundiran TO; Aghahowa ME; Brown BJ; Irabor DO
    West Afr J Med; 2003; 22(1):101-2. PubMed ID: 12769320
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Urological Findings in Beckwith-Wiedemann Syndrome With Chromosomal Duplications of 11p15.5: Evaluation and Management.
    Tong CC; Duffy KA; Chu DI; Weiss DA; Srinivasan AK; Canning DA; Kalish JM
    Urology; 2017 Feb; 100():224-227. PubMed ID: 27614119
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor.
    MacFarland SP; Duffy KA; Bhatti TR; Bagatell R; Balamuth NJ; Brodeur GM; Ganguly A; Mattei PA; Surrey LF; Balis FM; Kalish JM
    Pediatr Blood Cancer; 2018 Oct; 65(10):e27296. PubMed ID: 29932284
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.
    Cooper WN; Curley R; Macdonald F; Maher ER
    Genomics; 2007 May; 89(5):613-7. PubMed ID: 17337339
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.
    Bliek J; Maas S; Alders M; Merks JH; Mannens M
    J Pediatr; 2008 Jul; 153(1):95-100. PubMed ID: 18571544
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M; Pelosse B; Laroche L; Vazquez MP
    J Fr Ophtalmol; 2001 May; 24(5):479-81. PubMed ID: 11397983
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.