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.
152 related articles for article (PubMed ID: 29211059)
1. Improving clinical diagnosis in SHOX deficiency: the importance of growth velocity. Genoni G; Monzani A; Castagno M; Ricotti R; Rapa A; Petri A; Babu D; Giordano M; Prodam F; Bona G; Bellone S Pediatr Res; 2018 Feb; 83(2):438-444. PubMed ID: 29211059 [TBL] [Abstract][Full Text] [Related]
2. Prevalence of SHOX haploinsufficiency among short statured children. Marstrand-Joergensen MR; Jensen RB; Aksglaede L; Duno M; Juul A Pediatr Res; 2017 Feb; 81(2):335-341. PubMed ID: 27814343 [TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. SHOX deficiency in short Taiwanese children: A single-center experience. Tung YC; Lee NC; Hwu WL; Liu SY; Lee CT; Chien YH; Tsai WY J Formos Med Assoc; 2018 Oct; 117(10):909-914. PubMed ID: 29254682 [TBL] [Abstract][Full Text] [Related]
6. SHOX gene deletion screening by FISH in children with short stature and Madelung deformity and their characteristics. Kurnaz E; Savaş-Erdeve Ş; Çetinkaya S; Aycan Z J Pediatr Endocrinol Metab; 2018 Nov; 31(11):1273-1278. PubMed ID: 30332396 [TBL] [Abstract][Full Text] [Related]
7. Growth response to growth hormone treatment in patients with SHOX deficiency can be predicted by the Cologne prediction model. Hoyer-Kuhn H; Franklin J; Jones C; Blum WF; Schoenau E J Pediatr Endocrinol Metab; 2018 Jan; 31(1):25-31. PubMed ID: 29197219 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Novel Clinical Criteria Allow Detection of Short Stature Homeobox-Containing Gene Haploinsufficiency Caused by Either Gene or Enhancer Region Defects. Joustra SD; Kamp GA; Stalman SE; Donze SH; Losekoot M; Kant SG; de Bruin C; Oostdijk W; Wit JM Horm Res Paediatr; 2019; 92(6):372-381. PubMed ID: 32344414 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Short stature homeobox-containing gene duplications in 3.7% of girls with tall stature and normal karyotypes. Upners EN; Jensen RB; Rajpert-De Meyts E; Dunø M; Aksglaede L; Juul A Acta Paediatr; 2017 Oct; 106(10):1651-1657. PubMed ID: 28667773 [TBL] [Abstract][Full Text] [Related]
13. Pathogenic/likely pathogenic variants in the SHOX, GHR and IGFALS genes among Indian children with idiopathic short stature. Kumar A; Jain V; Chowdhury MR; Kumar M; Kaur P; Kabra M J Pediatr Endocrinol Metab; 2020 Jan; 33(1):79-88. PubMed ID: 31834863 [TBL] [Abstract][Full Text] [Related]
14. Height outcome of the recombinant human growth hormone treatment in patients with SHOX gene haploinsufficiency: a meta-analysis. Massart F; Bizzi M; Baggiani A; Miccoli M Pharmacogenomics; 2013 Apr; 14(6):607-12. PubMed ID: 23570464 [TBL] [Abstract][Full Text] [Related]
15. SHOX haploinsufficiency presenting with isolated short long bones in the second and third trimester. Ramachandrappa S; Kulkarni A; Gandhi H; Ellis C; Hutt R; Roberts L; Hamid R; Papageorghiou A; Mansour S Eur J Hum Genet; 2018 Mar; 26(3):350-358. PubMed ID: 29330548 [TBL] [Abstract][Full Text] [Related]
16. GH successful treatment in a female with a de novo 46,XX,add(X)(p36),t(X;Y)(p36.3;p11.2), growth impairment and SHOX-haploinsufficiency. Maggio MC; Corsello G Ital J Pediatr; 2019 Aug; 45(1):100. PubMed ID: 31412912 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Effect of 24 months of recombinant growth hormone on height and body proportions in SHOX haploinsufficiency. Munns CF; Berry M; Vickers D; Rappold GA; Hyland VJ; Glass IA; Batch JA J Pediatr Endocrinol Metab; 2003 Sep; 16(7):997-1004. PubMed ID: 14513876 [TBL] [Abstract][Full Text] [Related]
19. Short stature before puberty: which children should be screened for SHOX deficiency? Wolters B; Lass N; Wunsch R; Böckmann B; Austrup F; Reinehr T Horm Res Paediatr; 2013; 80(4):273-80. PubMed ID: 24051572 [TBL] [Abstract][Full Text] [Related]
20. Familial growth and skeletal features associated with SHOX haploinsufficiency. Munns CF; Glass IA; Flanagan S; Hayes M; Williams B; Berry M; Vickers D; O'Rourke P; Rao E; Rappold GA; Hyland VJ; Batch JA J Pediatr Endocrinol Metab; 2003 Sep; 16(7):987-96. PubMed ID: 14513875 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]