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 *

346 related articles for article (PubMed ID: 22702363)

  • 1. Epigenetic and genetic diagnosis of Silver-Russell syndrome.
    Eggermann T; Spengler S; Gogiel M; Begemann M; Elbracht M
    Expert Rev Mol Diagn; 2012 Jun; 12(5):459-71. PubMed ID: 22702363
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Broad clinical spectrum in Silver-Russell syndrome and consequences for genetic testing in growth retardation.
    Eggermann T; Gonzalez D; Spengler S; Arslan-Kirchner M; Binder G; Schönherr N
    Pediatrics; 2009 May; 123(5):e929-31. PubMed ID: 19364767
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Russell-Silver syndrome.
    Eggermann T
    Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):355-64. PubMed ID: 20803658
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome.
    Spengler S; Schönherr N; Binder G; Wollmann HA; Fricke-Otto S; Mühlenberg R; Denecke B; Baudis M; Eggermann T
    J Med Genet; 2010 May; 47(5):356-60. PubMed ID: 19762329
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Silver-Russell syndrome.
    Wakeling EL
    Arch Dis Child; 2011 Dec; 96(12):1156-61. PubMed ID: 21349887
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New developments in Silver-Russell syndrome and implications for clinical practice.
    Ishida M
    Epigenomics; 2016 Apr; 8(4):563-80. PubMed ID: 27066913
    [TBL] [Abstract][Full Text] [Related]  

  • 7. (Epi)mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation?
    Schönherr N; Meyer E; Eggermann K; Ranke MB; Wollmann HA; Eggermann T
    Eur J Med Genet; 2006; 49(5):414-8. PubMed ID: 16603426
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Silver-Russell syndrome: genetic basis and molecular genetic testing.
    Eggermann T; Begemann M; Binder G; Spengler S
    Orphanet J Rare Dis; 2010 Jun; 5():19. PubMed ID: 20573229
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic and epigenetic findings in Silver-Russell syndrome.
    Eggermann T; Begemann M; Spengler S; Schröder C; Kordass U; Binder G
    Pediatr Endocrinol Rev; 2010 Dec; 8(2):86-93. PubMed ID: 21150838
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.
    Bullman H; Lever M; Robinson DO; Mackay DJ; Holder SE; Wakeling EL
    J Med Genet; 2008 Jun; 45(6):396-9. PubMed ID: 18474587
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome.
    Eggermann T; Schönherr N; Eggermann K; Buiting K; Ranke MB; Wollmann HA; Binder G
    Clin Genet; 2008 Jan; 73(1):79-84. PubMed ID: 18070127
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.
    Lee BH; Kim GH; Oh TJ; Kim JH; Lee JJ; Choi SH; Lee JY; Kim JM; Choi IH; Kim YM; Choi JH; Yoo HW
    J Hum Genet; 2013 Sep; 58(9):604-10. PubMed ID: 23803580
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.
    Gicquel C; Rossignol S; Cabrol S; Houang M; Steunou V; Barbu V; Danton F; Thibaud N; Le Merrer M; Burglen L; Bertrand AM; Netchine I; Le Bouc Y
    Nat Genet; 2005 Sep; 37(9):1003-7. PubMed ID: 16086014
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Epigenetic regulation of growth: lessons from Silver-Russell syndrome.
    Eggermann T
    Endocr Dev; 2009; 14():10-9. PubMed ID: 19293571
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
    Inoue T; Nakamura A; Iwahashi-Odano M; Tanase-Nakao K; Matsubara K; Nishioka J; Maruo Y; Hasegawa Y; Suzumura H; Sato S; Kobayashi Y; Murakami N; Nakabayashi K; Yamazawa K; Fuke T; Narumi S; Oka A; Ogata T; Fukami M; Kagami M
    Clin Epigenetics; 2020 Jun; 12(1):86. PubMed ID: 32546215
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Testing of buccal swab DNA does not increase the detection rate for imprinting control region 1 hypomethylation in Silver-Russell syndrome.
    Spengler S; Begemann M; Binder G; Eggermann T
    Genet Test Mol Biomarkers; 2011 Oct; 15(10):725-6. PubMed ID: 21612428
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Silver-Russell syndrome.
    Binder G; Begemann M; Eggermann T; Kannenberg K
    Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):153-60. PubMed ID: 21396582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
    Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
    Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epigenetics in Silver-Russell syndrome.
    Rossignol S; Netchine I; Le Bouc Y; Gicquel C
    Best Pract Res Clin Endocrinol Metab; 2008 Jun; 22(3):403-14. PubMed ID: 18538282
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.