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Items: 1 to 20 of 27

1.

Reclassification of diabetes etiology in a family with multiple diabetes phenotypes.

Kavvoura FK, Raimondo A, Thanabalasingham G, Barrett A, Webster AL, Shears D, Mann NP, Ellard S, Gloyn AL, Owen KR.

J Clin Endocrinol Metab. 2014 Jun;99(6):E1067-71. doi: 10.1210/jc.2013-3641. Epub 2014 Feb 27.

2.

De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic cases.

Turan S, Ignatius J, Moilanen JS, Kuismin O, Stewart H, Mann NP, Linglart A, Bastepe M, Jüppner H.

J Clin Endocrinol Metab. 2012 Dec;97(12):E2314-9. doi: 10.1210/jc.2012-2920. Epub 2012 Oct 18.

3.

Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency.

Meimaridou E, Kowalczyk J, Guasti L, Hughes CR, Wagner F, Frommolt P, Nürnberg P, Mann NP, Banerjee R, Saka HN, Chapple JP, King PJ, Clark AJ, Metherell LA.

Nat Genet. 2012 May 27;44(7):740-2. doi: 10.1038/ng.2299.

4.

A patient with polyuria and hydronephrosis: question.

Jaureguiberry G, Van't Hoff W, Mushtaq I, Desai D, Mann NP, Kleta R, Bichet DG, Bockenhauer D.

Pediatr Nephrol. 2011 Nov;26(11):1977-8, 1979-80. doi: 10.1007/s00467-011-1780-6. Epub 2011 Feb 8. No abstract available.

PMID:
21301887
5.

How has research in the past 5 years changed my clinical practice?

Mann NP.

Arch Dis Child. 2008 Apr;93(4):327-30. Epub 2007 Sep 5. Review. No abstract available.

PMID:
17804593
6.

Cycle helmets.

Lee AJ, Mann NP.

Arch Dis Child. 2003 Jun;88(6):465-6. No abstract available.

7.

Current methods of transfer of young people with Type 1 diabetes to adult services.

Kipps S, Bahu T, Ong K, Ackland FM, Brown RS, Fox CT, Griffin NK, Knight AH, Mann NP, Neil HA, Simpson H, Edge JA, Dunger DB.

Diabet Med. 2002 Aug;19(8):649-54.

PMID:
12147145
9.

Serpentine fibula syndrome: expansion of the phenotype with three affected siblings.

Rosser EM, Mann NP, Hall CM, Winter RM.

Clin Dysmorphol. 1996 Apr;5(2):105-13. Review.

PMID:
8723560
10.

Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic mother.

Barnes PR, Kanabar DJ, Brueton L, Newsom-Davis J, Huson SM, Mann NP, Hilton-Jones D.

Neuromuscul Disord. 1995 Jan;5(1):59-65.

PMID:
7719143
11.

Gangrenous cholecystitis due to hepatitis A infection.

Black MM, Mann NP.

J Trop Med Hyg. 1992 Feb;95(1):73-4.

PMID:
1740824
12.

Organ donation.

Rutter N, Mann NP, Watson AR.

Arch Dis Child. 1989 Jun;64(6):875-8. No abstract available.

13.

Seasonal variation of haemoglobin A1 in children with insulin-dependent diabetes mellitus.

Hinde FR, Standen PJ, Mann NP, Johnston DI.

Eur J Pediatr. 1989 Jun;148(7):597-9.

PMID:
2629718
14.

Transient intracranial hypertension of infancy.

Mann NP, McLellan NJ, Cartlidge PH.

Arch Dis Child. 1988 Aug;63(8):966-8.

15.

Preoperative stabilisation in congenital diaphragmatic hernia.

Cartlidge PH, Mann NP, Kapila L.

Arch Dis Child. 1986 Dec;61(12):1226-8.

16.

Effect of night and day on preterm infants in a newborn nursery: randomised trial.

Mann NP, Haddow R, Stokes L, Goodley S, Rutter N.

Br Med J (Clin Res Ed). 1986 Nov 15;293(6557):1265-7.

17.

Improvement in metabolic control in diabetic adolescents by the use of increased insulin dose.

Mann NP, Johnston DI.

Diabetes Care. 1984 Sep-Oct;7(5):460-4.

PMID:
6389059
18.

A prospective study to evaluate the benefits of long-term self-monitoring of blood glucose in diabetic children.

Mann NP, Noronha JL, Johnston DI.

Diabetes Care. 1984 Jul-Aug;7(4):322-6.

PMID:
6381004
19.

A fifteen-month double-blind cross-over study of the efficacy and antigenicity of human and pork insulins.

Home PD, Mann NP, Hutchison AS, Park R, Walford S, Murphy M, Reeves WG.

Diabet Med. 1984 Jul;1(2):93-8.

PMID:
6086002
20.

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