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 *

55 related articles for article (PubMed ID: 23812911)

  • 1. 11p13 microduplication: a differential diagnosis of Silver-Russell syndrome?
    Amin AK; Krause J; Eggermann T
    Mol Cytogenet; 2024 Mar; 17(1):5. PubMed ID: 38486332
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Approach to the Patient With Suspected Silver-Russell Syndrome.
    Kurup U; Lim DBN; Palau H; Maharaj AV; Ishida M; Davies JH; Storr HL
    J Clin Endocrinol Metab; 2024 Sep; 109(10):e1889-e1901. PubMed ID: 38888172
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome.
    Maharaj AV; Cottrell E; Thanasupawat T; Joustra SD; Triggs-Raine B; Fujimoto M; Kant SG; van der Kaay D; Clement-de Boers A; Brooks AS; Aguirre GA; Martín Del Estal I; Castilla de Cortázar Larrea MI; Massoud A; van Duyvenvoorde HA; De Bruin C; Hwa V; Klonisch T; Hombach-Klonisch S; Storr HL
    JCI Insight; 2024 Feb; 9(6):. PubMed ID: 38516887
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Orthodontic management of patient with Silver-Russell Syndrome (SRS). A case report.
    Paglia M; Braiotta F; Quinzi V
    Eur J Paediatr Dent; 2024 Mar; 25(1):69-71. PubMed ID: 38357754
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome.
    Kvernebo Sunnergren K; Ankarberg-Lindgren C; Dahlgren J
    Front Endocrinol (Lausanne); 2019; 10():829. PubMed ID: 31920957
    [No Abstract]   [Full Text] [Related]  

  • 6. Hyperestrogenism Affects Adult Height Outcome in Growth Hormone Treated Boys With Silver-Russell Syndrome.
    Kvernebo-Sunnergren K; Ankarberg-Lindgren C; Åkesson K; Andersson MX; Samuelsson L; Lovmar L; Dahlgren J
    Front Endocrinol (Lausanne); 2018; 9():780. PubMed ID: 30622515
    [No Abstract]   [Full Text] [Related]  

  • 7. Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction.
    Abi Habib W; Brioude F; Edouard T; Bennett JT; Lienhardt-Roussie A; Tixier F; Salem J; Yuen T; Azzi S; Le Bouc Y; Harbison MD; Netchine I
    Genet Med; 2018 Feb; 20(2):250-258. PubMed ID: 28796236
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects.
    Inoue T; Nakamura A; Fuke T; Yamazawa K; Sano S; Matsubara K; Mizuno S; Matsukura Y; Harashima C; Hasegawa T; Nakajima H; Tsumura K; Kizaki Z; Oka A; Ogata T; Fukami M; Kagami M
    Clin Epigenetics; 2017; 9():52. PubMed ID: 28515796
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology.
    Õunap K
    Mol Syndromol; 2016 Jul; 7(3):110-21. PubMed ID: 27587987
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Diagnosis and management of Silver-Russell syndrome: first international consensus statement.
    Wakeling EL; Brioude F; Lokulo-Sodipe O; O'Connell SM; Salem J; Bliek J; Canton AP; Chrzanowska KH; Davies JH; Dias RP; Dubern B; Elbracht M; Giabicani E; Grimberg A; Grønskov K; Hokken-Koelega AC; Jorge AA; Kagami M; Linglart A; Maghnie M; Mohnike K; Monk D; Moore GE; Murray PG; Ogata T; Petit IO; Russo S; Said E; Toumba M; Tümer Z; Binder G; Eggermann T; Harbison MD; Temple IK; Mackay DJ; Netchine I
    Nat Rev Endocrinol; 2017 Feb; 13(2):105-124. PubMed ID: 27585961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome.
    Vals MA; Yakoreva M; Kahre T; Mee P; Muru K; Joost K; Teek R; Soellner L; Eggermann T; Õunap K
    Genet Test Mol Biomarkers; 2015 Dec; 19(12):684-91. PubMed ID: 26505556
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome.
    Azzi S; Salem J; Thibaud N; Chantot-Bastaraud S; Lieber E; Netchine I; Harbison MD
    J Med Genet; 2015 Jul; 52(7):446-53. PubMed ID: 25951829
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing.
    Eggermann T; Heilsberg AK; Bens S; Siebert R; Beygo J; Buiting K; Begemann M; Soellner L
    J Mol Med (Berl); 2014 Jul; 92(7):769-77. PubMed ID: 24658748
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing.
    Dias RP; Nightingale P; Hardy C; Kirby G; Tee L; Price S; Macdonald F; Barrett TG; Maher ER
    J Med Genet; 2013 Sep; 50(9):635-9. PubMed ID: 23812911
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.
    Kagami M; Mizuno S; Matsubara K; Nakabayashi K; Sano S; Fuke T; Fukami M; Ogata T
    Eur J Hum Genet; 2015 Aug; 23(8):1062-7. PubMed ID: 25351781
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology.
    Inoue T; Yagasaki H; Nishioka J; Nakamura A; Matsubara K; Narumi S; Nakabayashi K; Yamazawa K; Fuke T; Oka A; Ogata T; Fukami M; Kagami M
    J Med Genet; 2019 Jun; 56(6):413-418. PubMed ID: 30242100
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.