Wu JK - Search Results

1

Congenital thrombotic thrombocytopenic purpura (cTTP) with two novel mutations.

Prestidge TD, Rurali E, Wadsworth L, Wu JK, Moore JC, Bresin E. Prestidge TD, et al. Among authors: wu jk. Pediatr Blood Cancer. 2012 Dec 15;59(7):1296-8. doi: 10.1002/pbc.24159. Epub 2012 Apr 5. Pediatr Blood Cancer. 2012. PMID: 22488907

2

An assessment of published pediatric dosage guidelines for enoxaparin: a retrospective review.

Ho SH, Wu JK, Hamilton DP, Dix DB, Wadsworth LD. Ho SH, et al. Among authors: wu jk. J Pediatr Hematol Oncol. 2004 Sep;26(9):561-6. doi: 10.1097/01.mph.0000139453.22338.d9. J Pediatr Hematol Oncol. 2004. PMID: 15342982

3

Case 2: A pale infant - not a typical case of iron deficiency.

Wong MP, Wadsworth L, Wu JK, Dix D. Wong MP, et al. Among authors: wu jk. Paediatr Child Health. 2008 Jul;13(6):507-11. doi: 10.1093/pch/13.6.507a. Paediatr Child Health. 2008. PMID: 19436421 Free PMC article. No abstract available.

4

Hyperuricemia and reticulocytopenia in association with autoimmune hemolytic anemia in two children.

Jastaniah WA, Pritchard SL, Wu JK, Wadsworth LD. Jastaniah WA, et al. Among authors: wu jk. Am J Clin Pathol. 2004 Dec;122(6):849-54. doi: 10.1309/8DXD-VJT9-UN60-YACT. Am J Clin Pathol. 2004. PMID: 15539377

5

In Utero diagnosis and management of a fetus with homozygous α-Thalassemia in the second trimester: a case report and literature review.

Dwinnell SJ, Coad S, Butler B, Albersheim S, Wadsworth LD, Wu JK, Delisle MF. Dwinnell SJ, et al. Among authors: wu jk. J Pediatr Hematol Oncol. 2011 Dec;33(8):e358-60. doi: 10.1097/MPH.0b013e31821b368c. J Pediatr Hematol Oncol. 2011. PMID: 22042285 Review.

6

Utility of anti-xa monitoring in children receiving enoxaparin for therapeutic anticoagulation.

Leung M, Ho SH, Hamilton DP, Wu JK, Dix DB, Wadsworth LD, Ensom MH. Leung M, et al. Among authors: wu jk. J Pediatr Pharmacol Ther. 2005 Jan;10(1):43-50. doi: 10.5863/1551-6776-10.1.43. J Pediatr Pharmacol Ther. 2005. PMID: 23118625 Free PMC article.

7

Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion.

Hewitt J, Ballard JN, Nelson TN, Smith VC, Griffiths TA, Pritchard S, Wu JK, Wadsworth LD, Casey B, MacGillivray RT. Hewitt J, et al. Among authors: wu jk. Br J Haematol. 2005 Feb;128(3):380-5. doi: 10.1111/j.1365-2141.2004.05296.x. Br J Haematol. 2005. PMID: 15667541 Free article.

8

Molecular determination of the breakpoints of a 161 556 bp deletion at chromosome 13q34 that presented as severe factor VII deficiency in a neonate.

Hewitt J, Craven SJ, Brown LA, Bleackley MR, Ballard JN, Smith VC, Ofosu FA, Huntsman DG, Wadsworth LD, Wu JK, Macgillivray RT. Hewitt J, et al. Among authors: wu jk. Br J Haematol. 2008 Mar;140(5):589-92. doi: 10.1111/j.1365-2141.2007.06957.x. Epub 2007 Dec 19. Br J Haematol. 2008. PMID: 18162117 Free article. No abstract available.

9

A new method for characterization and epitope determination of a lupus anticoagulant-associated neutralizing antiprothrombin antibody.

Côté HC, Huntsman DG, Wu J, Wadsworth LD, MacGillivray RT. Côté HC, et al. Am J Clin Pathol. 1997 Feb;107(2):197-205. doi: 10.1093/ajcp/107.2.197. Am J Clin Pathol. 1997. PMID: 9024068

10

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.

Glogowska E, Schneider ER, Maksimova Y, Schulz VP, Lezon-Geyda K, Wu J, Radhakrishnan K, Keel SB, Mahoney D, Freidmann AM, Altura RA, Gracheva EO, Bagriantsev SN, Kalfa TA, Gallagher PG. Glogowska E, et al. Blood. 2017 Oct 19;130(16):1845-1856. doi: 10.1182/blood-2017-05-786004. Epub 2017 Jul 17. Blood. 2017. PMID: 28716860 Free PMC article.

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