BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 19724992)

  • 1. Imaging of SHOX-associated anomalies.
    Gahunia HK; Babyn PS; Kirsch S; Mendoza-Londono R
    Semin Musculoskelet Radiol; 2009 Sep; 13(3):236-54. PubMed ID: 19724992
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The SHOX gene and the short stature. Roundtable on diagnosis and treatment of short stature due to SHOX haploinsufficiency: how genetics, radiology and anthropometry can help the pediatrician in the diagnostic process Padova (April 20th, 2011).
    De Sanctis V; Tosetto I; Iughetti L; Antoniazzi F; Clementi M; Toffolutti T; Facchin P; Monti E; Pisanello L; Tonini G; Greggio NA
    Pediatr Endocrinol Rev; 2012 Aug; 9(4):727-33. PubMed ID: 23304810
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Auxology is a valuable instrument for the clinical diagnosis of SHOX haploinsufficiency in school-age children with unexplained short stature.
    Binder G; Ranke MB; Martin DD
    J Clin Endocrinol Metab; 2003 Oct; 88(10):4891-6. PubMed ID: 14557470
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of short stature caused by SHOX defects and therapeutic effect of recombinant human growth hormone.
    Binder G; Schwarze CP; Ranke MB
    J Clin Endocrinol Metab; 2000 Jan; 85(1):245-9. PubMed ID: 10634394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Short stature caused by isolated SHOX gene haploinsufficiency: update on the diagnosis and treatment.
    Jorge AA; Funari MF; Nishi MY; Mendonca BB
    Pediatr Endocrinol Rev; 2010 Dec; 8(2):79-85. PubMed ID: 21150837
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study].
    Dávid A; Butz H; Halász Z; Török D; Nyirő G; Muzsnai Á; Csákváry V; Luczay A; Sallai Á; Hosszú É; Felszeghy E; Tar A; Szántó Z; Fekete GL; Kun I; Patócs A; Bertalan R
    Orv Hetil; 2017 Aug; 158(34):1351-1356. PubMed ID: 28823207
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SHOX in short stature syndromes.
    Blaschke RJ; Rappold GA
    Horm Res; 2001; 55 Suppl 1():21-3. PubMed ID: 11408757
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.
    Rappold GA; Fukami M; Niesler B; Schiller S; Zumkeller W; Bettendorf M; Heinrich U; Vlachopapadoupoulou E; Reinehr T; Onigata K; Ogata T
    J Clin Endocrinol Metab; 2002 Mar; 87(3):1402-6. PubMed ID: 11889216
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency.
    Rappold G; Blum WF; Shavrikova EP; Crowe BJ; Roeth R; Quigley CA; Ross JL; Niesler B
    J Med Genet; 2007 May; 44(5):306-13. PubMed ID: 17182655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SHOX: growth, Léri-Weill and Turner syndromes.
    Blaschke RJ; Rappold GA
    Trends Endocrinol Metab; 2000 Aug; 11(6):227-30. PubMed ID: 10878753
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and Genetic Characteristics of 23 Korean Patients with Haploinsufficiency of the Short-stature Homeobox-containing Gene.
    Lee JS; Kim HY; Lee YA; Lee SY; Cho TJ; Ko JM
    Exp Clin Endocrinol Diabetes; 2021 Aug; 129(8):611-620. PubMed ID: 32932528
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.
    Binder G; Renz A; Martinez A; Keselman A; Hesse V; Riedl SW; Häusler G; Fricke-Otto S; Frisch H; Heinrich JJ; Ranke MB
    J Clin Endocrinol Metab; 2004 Sep; 89(9):4403-8. PubMed ID: 15356038
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Short stature due to SHOX deficiency: genotype, phenotype, and therapy.
    Binder G
    Horm Res Paediatr; 2011 Feb; 75(2):81-9. PubMed ID: 21325865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Short stature caused by SHOX gene haploinsufficiency: from diagnosis to treatment].
    Jorge AA; Nishi MY; Funari MF; Souza SC; Arnhold IJ; Mendonça BB
    Arq Bras Endocrinol Metabol; 2008 Jul; 52(5):765-73. PubMed ID: 18797583
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SHOX at a glance: from gene to protein.
    Marchini A; Rappold G; Schneider KU
    Arch Physiol Biochem; 2007 Jun; 113(3):116-23. PubMed ID: 17922307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and radiological characteristics of 22 children with SHOX anomalies and familial short stature suggestive of Léri-Weill Dyschondrosteosis.
    Salmon-Musial AS; Rosilio M; David M; Huber C; Pichot E; Cormier-Daire V; Nicolino M
    Horm Res Paediatr; 2011; 76(3):178-85. PubMed ID: 21912078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unique deletion in exon 5 of SHOX gene in a patient with idiopathic short stature.
    Shanske AL; Puri M; Marshall B; Saenger P
    Horm Res; 2007; 67(2):61-6. PubMed ID: 17028440
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SHOX haploinsufficiency and its modifying factors.
    Ogata T
    J Pediatr Endocrinol Metab; 2002 Dec; 15 Suppl 5():1289-94. PubMed ID: 12510982
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Langer's mesomelic dysplasia: a case report.
    Aggarwal V; Aggarwal N; Venkat B
    J Pediatr Orthop B; 2014 Mar; 23(2):200-2. PubMed ID: 23863349
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of
    Gürsoy S; Hazan F; Aykut A; Nalbantoğlu Ö; Korkmaz HA; Demir K; Özkan B; Çoğulu Ö
    J Clin Res Pediatr Endocrinol; 2020 Nov; 12(4):358-365. PubMed ID: 32295321
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.