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Items: 11

1.

White matter integrity and processing speed in sickle cell anemia.

Stotesbury H, Kirkham FJ, Kölbel M, Balfour P, Clayden JD, Sahota S, Sakaria S, Saunders DE, Howard J, Kesse-Adu R, Inusa B, Pelidis M, Chakravorty S, Rees DC, Awogbade M, Wilkey O, Layton M, Clark CA, Kawadler JM.

Neurology. 2018 May 11. pii: 10.1212/WNL.0000000000005644. doi: 10.1212/WNL.0000000000005644. [Epub ahead of print]

PMID:
29752305
2.

Refractory severe immune thrombocytopenia in a twin pregnancy.

Harrington P, Nelson-Piercy C, Williamson C, Cooper N, Kesse-Adu R, Robinson S.

Obstet Med. 2018 Mar;11(1):35-38. doi: 10.1177/1753495X17709188. Epub 2017 Jul 10.

PMID:
29636813
3.

g(HbF): a genetic model of fetal hemoglobin in sickle cell disease.

Gardner K, Fulford T, Silver N, Rooks H, Angelis N, Allman M, Nkya S, Makani J, Howard J, Kesse-Adu R, Rees DC, Stuart-Smith S, Yeghen T, Awogbade M, Sangeda RZ, Mgaya J, Patel H, Newhouse S, Menzel S, Thein SL.

Blood Adv. 2018 Feb 13;2(3):235-239. doi: 10.1182/bloodadvances.2017009811.

4.

A descriptive study of the characteristics of older adults with sickle cell disease.

Khan AB, Kesse-Adu R, Breen C, Murphy PB, Chambers J, Holmes P, Howard J.

Am J Hematol. 2018 Feb;93(2):E38-E40. doi: 10.1002/ajh.24961. Epub 2017 Nov 20. No abstract available.

PMID:
29098717
5.

The utility of thromboelastography and thrombin generation in assessing the prothrombotic state of adults with sickle cell disease.

Wijnberge M, Parmar K, Kesse-Adu R, Howard J, Cohen AT, Hunt BJ.

Thromb Res. 2017 Oct;158:113-120. doi: 10.1016/j.thromres.2017.08.020. Epub 2017 Sep 6.

PMID:
28888622
6.

Effect of N-acetylcysteine on pain in daily life in patients with sickle cell disease: a randomised clinical trial.

Sins JWR, Fijnvandraat K, Rijneveld AW, Boom MB, Kerkhoffs JH, van Meurs AH, de Groot MR, Heijboer H, Dresse MF, Lê PQ, Hermans P, Vanderfaeillie A, Van Den Neste EW, Benghiat FS, Kesse-Adu R, Delannoy A, Efira A, Azerad MA, de Borgie CA, Biemond BJ.

Br J Haematol. 2017 Jun 23. doi: 10.1111/bjh.14809. [Epub ahead of print] No abstract available.

PMID:
28643376
7.

Intracranial Aneurysms in Sickle-Cell Disease Are Associated With the Hemoglobin SS Genotype But Not With Moyamoya Syndrome.

Birkeland P, Gardner K, Kesse-Adu R, Davies J, Lauritsen J, Rom Poulsen F, Tolias CM, Thein SL.

Stroke. 2016 Jul;47(7):1710-3. doi: 10.1161/STROKEAHA.116.012664. Epub 2016 Jun 14.

8.

Cementless total hip replacements in sickle cell disease.

Jack CM, Howard J, Aziz ES, Kesse-Adu R, Bankes MJ.

Hip Int. 2016 Mar-Apr;26(2):186-92. doi: 10.5301/hipint.5000317. Epub 2015 Dec 14.

PMID:
26692246
9.

Immune reconstitution inflammatory syndrome in a patient with HIV presenting as severe mixed haemolytic anaemia.

Mwirigi A, Stockwell S, Radia D, Kulasegaram R, Kesse-Adu R.

Int J STD AIDS. 2016 Oct;27(11):1019-22. doi: 10.1177/0956462415611521. Epub 2015 Oct 13.

PMID:
26468273
10.

Low flow nocturnal oxygen therapy does not suppress haemoglobin levels or increase painful crises in sickle cell disease.

Ip H, Kesse-Adu R, Howard J, Hart N.

Br J Haematol. 2013 May;161(3):455-6. doi: 10.1111/bjh.12254. Epub 2013 Feb 19. No abstract available.

PMID:
23419066
11.

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