Shaw N - Search Results

1

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. Among authors: shaw n. Acta Paediatr. 2004 Sep;93(9):1195-201. Acta Paediatr. 2004. PMID: 15384883 Review.

2

Investigation and outcome of neonatal hepatitis in infants with hypopituitarism.

Spray CH, Mckiernan P, Waldron KE, Shaw N, Kirk J, Kelly DA. Spray CH, et al. Among authors: shaw n. Acta Paediatr. 2000 Aug;89(8):951-4. doi: 10.1080/080352500750043413. Acta Paediatr. 2000. PMID: 10976837

3

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

4

Diabetic ketoacidosis in Asian children.

Alvi NS, Davies P, Kirk JM, Shaw NJ. Alvi NS, et al. Among authors: shaw nj. Arch Dis Child. 2001 Jul;85(1):60-1. doi: 10.1136/adc.85.1.60. Arch Dis Child. 2001. PMID: 11420205 Free PMC article.

5

Type 2 diabetes mellitus in UK children--an emerging problem.

Ehtisham S, Barrett TG, Shaw NJ. Ehtisham S, et al. Among authors: shaw nj. Diabet Med. 2000 Dec;17(12):867-71. doi: 10.1046/j.1464-5491.2000.00409.x. Diabet Med. 2000. PMID: 11168330

6

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. Eur J Endocrinol. 2021 May;184(5):K15-K20. doi: 10.1530/EJE-20-0152. Eur J Endocrinol. 2021. PMID: 33690157

7

Factors determining patient choice of device for GH therapy.

Wickramasuriya BP, Casey A, Akhtar S, Zia R, Ehtisham S, Barrett TG, Shaw NJ, Kirk JM. Wickramasuriya BP, et al. Among authors: shaw nj. Horm Res. 2006;65(1):18-22. doi: 10.1159/000090375. Epub 2005 Dec 16. Horm Res. 2006. PMID: 16357486

8

Asian MODY: are we missing an important diagnosis?

Porter JR, Rangasami JJ, Ellard S, Gloyn AL, Shields BM, Edwards J, Anderson JM, Shaw NJ, Hattersley AT, Frayling TM, Plunkett M, Barrett TG. Porter JR, et al. Among authors: shaw nj. Diabet Med. 2006 Nov;23(11):1257-60. doi: 10.1111/j.1464-5491.2006.01958.x. Diabet Med. 2006. PMID: 17054605

9

Permanent neonatal diabetes in an Asian infant.

Porter JR, Shaw NJ, Barrett TG, Hattersley AT, Ellard S, Gloyn AL. Porter JR, et al. Among authors: shaw nj. J Pediatr. 2005 Jan;146(1):131-3. doi: 10.1016/j.jpeds.2004.09.008. J Pediatr. 2005. PMID: 15644838 Review.

10

Hypopituitarism in children with cerebral palsy.

Uday S, Shaw N, Krone R, Kirk J. Uday S, et al. Among authors: shaw n. Arch Dis Child. 2017 Jun;102(6):559-561. doi: 10.1136/archdischild-2016-311012. Epub 2016 Oct 27. Arch Dis Child. 2017. PMID: 27789461

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