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Items: 16

1.

Difficulties in selecting an appropriate neonatal thyroid stimulating hormone (TSH) screening threshold.

Korada SM, Pearce M, Ward Platt MP, Avis E, Turner S, Wastell H, Cheetham T.

Arch Dis Child. 2010 Mar;95(3):169-73. doi: 10.1136/adc.2008.147884. Epub 2009 Aug 12.

PMID:
19679574
2.

Second trimester maternal serum ADAM12 levels in Down's syndrome pregnancies.

Donalson K, Turner S, Wastell H, Cuckle H.

Prenat Diagn. 2008 Oct;28(10):904-7. doi: 10.1002/pd.2043.

PMID:
18785180
3.

Repeat testing for congenital hypothyroidism in preterm infants is unnecessary with an appropriate thyroid stimulating hormone threshold.

Korada M, Pearce MS, Ward Platt MP, Avis E, Turner S, Wastell H, Cheetham T.

Arch Dis Child Fetal Neonatal Ed. 2008 Jul;93(4):F286-8. doi: 10.1136/adc.2007.134999. Epub 2008 Feb 5.

PMID:
18252816
4.

A study to determine the minimum volume of blood necessary to be discarded from a central venous catheter before a valid sample is obtained in children with cancer.

Cole M, Price L, Parry A, Picton S, Waters F, Marshall S, Goran C, Parnham A, Wastell H, Reid MM, Pearson AD, Boddy AV, Veal GJ.

Pediatr Blood Cancer. 2007 Jun 15;48(7):687-95.

PMID:
16676305
5.

An investigation into the need for supplementary steroids in organ transplant patients undergoing gingival surgery. A double-blind, split-mouth, cross-over study.

Thomason JM, Girdler NM, Kendall-Taylor P, Wastell H, Weddel A, Seymour RA.

J Clin Periodontol. 1999 Sep;26(9):577-82.

PMID:
10487307
6.
7.

CSF and plasma amino acid levels in motor neuron disease: elevation of CSF glutamate in a subset of patients.

Shaw PJ, Forrest V, Ince PG, Richardson JP, Wastell HJ.

Neurodegeneration. 1995 Jun;4(2):209-16.

PMID:
7583686
8.

Biotinidase deficiency: a survey of 10 cases.

Wastell HJ, Bartlett K, Dale G, Shein A.

Arch Dis Child. 1988 Oct;63(10):1244-9.

9.

Hormone studies in a case of virilisation due to ovarian tumour.

Fleetwood JA, Watson MJ, Wastell HJ, Weddell A.

Ann Clin Biochem. 1985 Sep;22 ( Pt 5):498-501.

PMID:
2998262
10.

Enzyme studies in combined carboxylase deficiency.

Bartlett K, Ghneim HK, Stirk JH, Wastell HJ, Sherratt HS, Leonard JV.

Ann N Y Acad Sci. 1985 Jun;447(1):235-51. doi: 10.1111/j.1749-6632.1985.tb18442.x. No abstract available.

PMID:
25572128
11.

Enzyme studies in biotin-responsive disorders.

Bartlett K, Ghneim HK, Stirk HJ, Wastell H.

J Inherit Metab Dis. 1985;8 Suppl 1:46-52. Review.

PMID:
2864473
12.

Enzyme studies in combined carboxylase deficiency.

Bartlett K, Ghneim HK, Stirk JH, Wastell HJ, Sherratt HS, Leonard JV.

Ann N Y Acad Sci. 1985;447:235-51. No abstract available.

PMID:
2861780
13.
15.

Transferrin variants in the Indian subcontinent.

Papiha SS, Wastell HJ.

Humangenetik. 1974 Jan 22;21(1):69-73. No abstract available.

PMID:
4837514
16.

Mr. Wastell's Case of Thoracic Suppuration.

Wastell H.

Med Phys J. 1803 May 1;9(51):426-433. No abstract available.

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