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Results: 18

1.

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome).

Belin V, Cusin V, Viot G, Girlich D, Toutain A, Moncla A, Vekemans M, Le Merrer M, Munnich A, Cormier-Daire V.

Nat Genet. 1998 May;19(1):67-9.

PMID:
9590292
[PubMed - indexed for MEDLINE]
2.

[From gene to disease; from SHOX to Lèri-Weill dyschondrosteosis, Turner syndrome and idiopathic short stature].

Kant SG, Drop SL.

Ned Tijdschr Geneeskd. 2001 Jul 28;145(30):1456-9. Review. Dutch.

PMID:
11503314
[PubMed - indexed for MEDLINE]
3.

SHOX: pseudoautosomal homeobox containing gene for short stature and dyschondrosteosis.

Ogata T.

Growth Horm IGF Res. 1999 Jun;9 Suppl B:53-7; discussion 57-8. Review.

PMID:
10549307
[PubMed - indexed for MEDLINE]
4.

Short stature and dysmorphology associated with defects in the SHOX gene.

Leka SK, Kitsiou-Tzeli S, Kalpini-Mavrou A, Kanavakis E.

Hormones (Athens). 2006 Apr-Jun;5(2):107-18. Review.

PMID:
16807223
[PubMed - indexed for MEDLINE]
Free Article
5.

SHOX: growth, Léri-Weill and Turner syndromes.

Blaschke RJ, Rappold GA.

Trends Endocrinol Metab. 2000 Aug;11(6):227-30. Review.

PMID:
10878753
[PubMed - indexed for MEDLINE]
6.
7.

SHOX at a glance: from gene to protein.

Marchini A, Rappold G, Schneider KU.

Arch Physiol Biochem. 2007 Jun;113(3):116-23. Review.

PMID:
17922307
[PubMed - indexed for MEDLINE]
8.

[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. Review. Portuguese.

PMID:
18797583
[PubMed - indexed for MEDLINE]
Free Article
9.

SHOX in short stature syndromes.

Blaschke RJ, Rappold GA.

Horm Res. 2001;55 Suppl 1:21-3. Review.

PMID:
11408757
[PubMed - indexed for MEDLINE]
10.

Short stature due to SHOX deficiency: genotype, phenotype, and therapy.

Binder G.

Horm Res Paediatr. 2011 Feb;75(2):81-9. doi: 10.1159/000324105. Epub 2011 Feb 4. Review.

PMID:
21325865
[PubMed - indexed for MEDLINE]
Free Article
11.

SHOX haploinsufficiency and its modifying factors.

Ogata T.

J Pediatr Endocrinol Metab. 2002 Dec;15 Suppl 5:1289-94. Review.

PMID:
12510982
[PubMed - indexed for MEDLINE]
12.

SHOX gene in Leri-Weill syndrome and in idiopathic short stature.

Bernasconi S, Mariani S, Falcinelli C, Milioli S, Iughetti L, Forabosco A.

J Endocrinol Invest. 2001 Oct;24(9):737-41. Review. No abstract available.

PMID:
11716161
[PubMed - indexed for MEDLINE]
13.

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. Review.

PMID:
21150837
[PubMed - indexed for MEDLINE]
14.

Imaging of SHOX-associated anomalies.

Gahunia HK, Babyn PS, Kirsch S, Mendoza-Londono R.

Semin Musculoskelet Radiol. 2009 Sep;13(3):236-54. doi: 10.1055/s-0029-1237691. Epub 2009 Sep 1. Review.

PMID:
19724992
[PubMed - indexed for MEDLINE]
15.

Genetic studies in idiopathic short stature.

Attie KM.

Curr Opin Pediatr. 2000 Aug;12(4):400-4. Review.

PMID:
10943824
[PubMed - indexed for MEDLINE]
16.

The role of the SHOX gene in the pathophysiology of Turner syndrome.

Oliveira CS, Alves C.

Endocrinol Nutr. 2011 Oct;58(8):433-42. doi: 10.1016/j.endonu.2011.06.005. Epub 2011 Sep 16. Review.

PMID:
21925981
[PubMed - indexed for MEDLINE]
17.

[SHOX haploinsufficiency].

Ogata T.

Nihon Rinsho. 2006 May 28;Suppl 1:105-10. Review. Japanese. No abstract available.

PMID:
16776105
[PubMed - indexed for MEDLINE]
18.

[Leri-Weill syndrome].

Ogata T, Fukami M.

Nihon Rinsho. 2006 Sep 28;Suppl 3:427-32. Review. Japanese. No abstract available.

PMID:
17022580
[PubMed - indexed for MEDLINE]

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