Almeida A - Search Results

1

Unusual presentation of factor XIII deficiency.

Almeida A, Khair K, Hann I, Liesner R. Almeida A, et al. Haemophilia. 2002 Sep;8(5):703-5. doi: 10.1046/j.1365-2516.2002.00658.x. Haemophilia. 2002. PMID: 12199683

2

The use of recombinant factor VIIa in children with inherited platelet function disorders.

Almeida AM, Khair K, Hann I, Liesner R. Almeida AM, et al. Br J Haematol. 2003 May;121(3):477-81. doi: 10.1046/j.1365-2141.2003.04286.x. Br J Haematol. 2003. PMID: 12716372 Free article.

3

Targeted therapy for inherited GPI deficiency.

Almeida AM, Murakami Y, Baker A, Maeda Y, Roberts IA, Kinoshita T, Layton DM, Karadimitris A. Almeida AM, et al. N Engl J Med. 2007 Apr 19;356(16):1641-7. doi: 10.1056/NEJMoa063369. N Engl J Med. 2007. PMID: 17442906 Free article.

4

Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency.

Almeida AM, Murakami Y, Layton DM, Hillmen P, Sellick GS, Maeda Y, Richards S, Patterson S, Kotsianidis I, Mollica L, Crawford DH, Baker A, Ferguson M, Roberts I, Houlston R, Kinoshita T, Karadimitris A. Almeida AM, et al. Nat Med. 2006 Jul;12(7):846-51. doi: 10.1038/nm1410. Epub 2006 Jun 11. Nat Med. 2006. PMID: 16767100

5

Thromboprophylaxis with unmonitored intermediate-dose low molecular weight heparin in pregnancies with a previous arterial or venous thrombotic event.

Hunt BJ, Gattens M, Khamashta M, Nelson-Piercy C, Almeida A. Hunt BJ, et al. Among authors: almeida a. Blood Coagul Fibrinolysis. 2003 Dec;14(8):735-9. doi: 10.1097/00001721-200312000-00007. Blood Coagul Fibrinolysis. 2003. PMID: 14614352 Clinical Trial.

6

Therapeutic challenges in childhood sickle cell disease. Part 1: current and future treatment options.

Amrolia PJ, Almeida A, Halsey C, Roberts IA, Davies SC. Amrolia PJ, et al. Among authors: almeida a. Br J Haematol. 2003 Mar;120(5):725-36. doi: 10.1046/j.1365-2141.2003.04143.x. Br J Haematol. 2003. PMID: 12614202 Free article. Review. No abstract available.

7

Therapeutic challenges in childhood sickle cell disease. Part 2: a problem-orientated approach.

Amrolia PJ, Almeida A, Davies SC, Roberts IA. Amrolia PJ, et al. Among authors: almeida a. Br J Haematol. 2003 Mar;120(5):737-43. doi: 10.1046/j.1365-2141.2003.04144.x. Br J Haematol. 2003. PMID: 12614203 Free article. Review. No abstract available.

8

Neonatal screening for haemoglobinopathies: the results of a 10-year programme in an English Health Region.

Almeida AM, Henthorn JS, Davies SC. Almeida AM, et al. Br J Haematol. 2001 Jan;112(1):32-5. doi: 10.1046/j.1365-2141.2001.02512.x. Br J Haematol. 2001. PMID: 11167779 Free article.

9

Cell-type-specific transcriptional regulation of PIGM underpins the divergent hematologic phenotype in inherited GPl deficiency.

Costa JR, Caputo VS, Makarona K, Layton DM, Roberts IA, Almeida AM, Karadimitris A. Costa JR, et al. Among authors: almeida am. Blood. 2014 Nov 13;124(20):3151-4. doi: 10.1182/blood-2014-09-598813. Epub 2014 Oct 7. Blood. 2014. PMID: 25293775 Free PMC article.

10

Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformation.

McCloy M, Almeida A, Daly P, Vulliamy T, Roberts IA, Dokal I. McCloy M, et al. Among authors: almeida a. Br J Haematol. 2001 Feb;112(2):427-9. doi: 10.1046/j.1365-2141.2001.02585.x. Br J Haematol. 2001. PMID: 11167843 Free article.

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