Owen C - Search Results

1

Testosterone Treatment of Pubertal Delay in Duchenne Muscular Dystrophy.

Wood CL, Cheetham TD, Guglieri M, Bushby K, Owen C, Johnstone H, Straub V. Wood CL, et al. Among authors: owen c. Neuropediatrics. 2015 Dec;46(6):371-6. doi: 10.1055/s-0035-1563696. Epub 2015 Sep 26. Neuropediatrics. 2015. PMID: 26408798

2

Prophylactic oral bisphosphonate therapy in duchenne muscular dystrophy.

Srinivasan R, Rawlings D, Wood CL, Cheetham T, Moreno AC, Mayhew A, Eagle M, Guglieri M, Straub V, Owen C, Bushby K, Sarkozy A. Srinivasan R, et al. Among authors: owen c. Muscle Nerve. 2016 Jun;54(1):79-85. doi: 10.1002/mus.24991. Epub 2016 Apr 27. Muscle Nerve. 2016. PMID: 26599341

3

Diagnosis and management of polyendocrinopathy syndromes.

Owen CJ, Cheetham TD. Owen CJ, et al. Endocrinol Metab Clin North Am. 2009 Jun;38(2):419-36, x. doi: 10.1016/j.ecl.2009.01.007. Endocrinol Metab Clin North Am. 2009. PMID: 19328420 Review.

4

Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.

Owen CJ, Jennings CE, Imrie H, Lachaux A, Bridges NA, Cheetham TD, Pearce SH. Owen CJ, et al. J Clin Endocrinol Metab. 2003 Dec;88(12):6034-9. doi: 10.1210/jc.2003-031080. J Clin Endocrinol Metab. 2003. PMID: 14671208

5

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.

Owen CJ, Eden JA, Jennings CE, Wilson V, Cheetham TD, Pearce SH. Owen CJ, et al. J Mol Endocrinol. 2006 Aug;37(1):97-104. doi: 10.1677/jme.1.02072. J Mol Endocrinol. 2006. PMID: 16901927

6

Discordance for X-linked hypophosphataemic rickets in identical twin girls.

Owen CJ, Habeb A, Pearce SH, Wright M, Ichikawa S, Sorenson AH, Econs MJ, Cheetham TD. Owen CJ, et al. Horm Res. 2009;71(4):237-44. doi: 10.1159/000201113. Epub 2009 Mar 4. Horm Res. 2009. PMID: 19258716

7

[No title available]

[No authors listed] [No authors listed] PMID: 32978144

8

Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.

Sutherland A, Davies J, Owen CJ, Vaikkakara S, Walker C, Cheetham TD, James RA, Perros P, Donaldson PT, Cordell HJ, Quinton R, Pearce SH. Sutherland A, et al. Among authors: owen cj. J Clin Endocrinol Metab. 2007 Aug;92(8):3338-41. doi: 10.1210/jc.2007-0173. Epub 2007 May 29. J Clin Endocrinol Metab. 2007. PMID: 17535987 Free PMC article.

9

Role of the CD40 locus in Graves' disease.

Houston FA, Wilson V, Jennings CE, Owen CJ, Donaldson P, Perros P, Pearce SH. Houston FA, et al. Thyroid. 2004 Jul;14(7):506-9. doi: 10.1089/1050725041517039. Thyroid. 2004. PMID: 15307939

10

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, Donaldson PT, Ball SG, James RA, Quinton R, Perros P, Pearce SH. Velaga MR, et al. Among authors: owen cj. J Clin Endocrinol Metab. 2004 Nov;89(11):5862-5. doi: 10.1210/jc.2004-1108. J Clin Endocrinol Metab. 2004. PMID: 15531553

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