Shaw NJ - Search Results

1

TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis.

Cangul H, Aycan Z, Saglam H, Forman JR, Cetinkaya S, Tarim O, Bober E, Cesur Y, Kurtoglu S, Darendeliler F, Bas V, Eren E, Demir K, Kiraz A, Aydin BK, Karthikeyan A, Kendall M, Boelaert K, Shaw NJ, Kirk J, Högler W, Barrett TG, Maher ER. Cangul H, et al. Among authors: shaw nj. J Pediatr Endocrinol Metab. 2012;25(5-6):419-26. doi: 10.1515/jpem-2012-0053. J Pediatr Endocrinol Metab. 2012. PMID: 22876533

2

Clinical characteristics and treatment requirements of children with autosomal recessive pseudohypoaldosteronism.

Bandhakavi M, Wanaguru A, Ayuk L, Kirk JM, Barrett TG, Kershaw M, Högler W, Shaw NJ. Bandhakavi M, et al. Among authors: shaw nj. Eur J Endocrinol. 2021 May;184(5):K15-K20. doi: 10.1530/EJE-20-0152. Eur J Endocrinol. 2021. PMID: 33690157

3

Childhood growth hormone deficiency, bone density, structures and fractures: scrutinizing the evidence.

Högler W, Shaw N. Högler W, et al. Clin Endocrinol (Oxf). 2010 Mar;72(3):281-9. doi: 10.1111/j.1365-2265.2009.03686.x. Epub 2009 Aug 29. Clin Endocrinol (Oxf). 2010. PMID: 19719765 Review.

4

Relationship between serum 25-hydroxyvitamin D and parathyroid hormone in the search for a biochemical definition of vitamin D deficiency in children.

Atapattu N, Shaw N, Högler W. Atapattu N, et al. Pediatr Res. 2013 Nov;74(5):552-6. doi: 10.1038/pr.2013.139. Epub 2013 Sep 2. Pediatr Res. 2013. PMID: 23999068

5

Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.

Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, Kirk JM. Rainbow LA, et al. Among authors: shaw nj. Clin Endocrinol (Oxf). 2005 Feb;62(2):163-8. doi: 10.1111/j.1365-2265.2004.02189.x. Clin Endocrinol (Oxf). 2005. PMID: 15670191

6

Clinical characteristics and management of cranial diabetes insipidus in infants.

Karthikeyan A, Abid N, Sundaram PC, Shaw NJ, Barrett TG, Högler W, Kirk JM. Karthikeyan A, et al. Among authors: shaw nj. J Pediatr Endocrinol Metab. 2013;26(11-12):1041-6. doi: 10.1515/jpem-2013-0026. J Pediatr Endocrinol Metab. 2013. PMID: 23751384

7

Estradiol: micrograms or milligrams.

Kirk JM, Wickramasuriya N, Shaw NJ. Kirk JM, et al. Among authors: shaw nj. Endocrinol Diabetes Metab Case Rep. 2016;2016:150096. doi: 10.1530/EDM-15-0096. Epub 2016 Jan 6. Endocrinol Diabetes Metab Case Rep. 2016. PMID: 26843960 Free PMC article.

8

Causes, patterns and severity of androgen excess in 487 consecutively recruited pre- and post-pubertal children.

Idkowiak J, Elhassan YS, Mannion P, Smith K, Webster R, Saraff V, Barrett TG, Shaw NJ, Krone N, Dias RP, Kershaw M, Kirk JM, Högler W, Krone RE, O'Reilly MW, Arlt W. Idkowiak J, et al. Among authors: shaw nj. Eur J Endocrinol. 2019 Mar 1;180(3):213-221. doi: 10.1530/EJE-18-0854. Eur J Endocrinol. 2019. PMID: 30566905 Free PMC article.

9

Ethnic differences in insulin resistance and body composition in United Kingdom adolescents.

Ehtisham S, Crabtree N, Clark P, Shaw N, Barrett T. Ehtisham S, et al. J Clin Endocrinol Metab. 2005 Jul;90(7):3963-9. doi: 10.1210/jc.2004-2001. Epub 2005 Apr 19. J Clin Endocrinol Metab. 2005. PMID: 15840754

10

Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature.

Iyer S, Korada M, Rainbow L, Kirk J, Brown RM, Shaw N, Barrett TG. Iyer S, et al. Acta Paediatr. 2004 Sep;93(9):1195-201. Acta Paediatr. 2004. PMID: 15384883 Review.

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