Old J - Search Results

1

Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing.

Haywood A, Dreau H, Timbs A, Schuh A, Old J, Henderson S. Haywood A, et al. Among authors: old j. Ann Hematol. 2010 Dec;89(12):1215-21. doi: 10.1007/s00277-010-1013-2. Epub 2010 Jun 22. Ann Hematol. 2010. PMID: 20567827

2

Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotyping.

Timbs AT, Rugless MJ, Gallienne AE, Haywood AM, Henderson SJ, Old JM. Timbs AT, et al. Among authors: old jm. Hemoglobin. 2012;36(2):144-50. doi: 10.3109/03630269.2011.647998. Epub 2012 Jan 12. Hemoglobin. 2012. PMID: 22239406

3

Haemoglobin (Hb) G-Philadelphia, Hb Stanleyville-II, Hb G-Norfolk, Hb Matsue-Oki and Hb Mizushi can form a panel of α-chain variants that overlap in their phenotype: the novel use of StyI to screen for Hb G-Philadelphia.

Khalil MS, Timbs A, Henderson S, Schuh A, Hussein MR, Old J. Khalil MS, et al. Among authors: old j. Int J Lab Hematol. 2011 Jun;33(3):318-25. doi: 10.1111/j.1751-553X.2010.01289.x. Epub 2011 Jan 26. Int J Lab Hematol. 2011. PMID: 21266019

4

Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.

Moradkhani K, Préhu C, Old J, Henderson S, Balamitsa V, Luo HY, Poon MC, Chui DH, Wajcman H, Patrinos GP. Moradkhani K, et al. Among authors: old j. Ann Hematol. 2009 Jun;88(6):535-43. doi: 10.1007/s00277-008-0624-3. Epub 2008 Oct 16. Ann Hematol. 2009. PMID: 18923834 Free PMC article.

5

Molecular diagnostics for haemoglobinopathies.

Old J, Henderson S. Old J, et al. Expert Opin Med Diagn. 2010 May;4(3):225-40. doi: 10.1517/17530051003709729. Epub 2010 Mar 15. Expert Opin Med Diagn. 2010. PMID: 23488532

6

Incidence of haemoglobinopathies in various populations - the impact of immigration.

Henderson S, Timbs A, McCarthy J, Gallienne A, Van Mourik M, Masters G, May A, Khalil MS, Schuh A, Old J. Henderson S, et al. Among authors: old j. Clin Biochem. 2009 Dec;42(18):1745-56. doi: 10.1016/j.clinbiochem.2009.05.012. Epub 2009 Jun 1. Clin Biochem. 2009. PMID: 19497317

7

A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2.

Khalil MS, Marouf S, Element D, Timbs A, Gallienne A, Schuh A, Old JM, Henderson S. Khalil MS, et al. Hemoglobin. 2014;38(3):201-6. doi: 10.3109/03630269.2014.885908. Epub 2014 Mar 6. Hemoglobin. 2014. PMID: 24601842

8

Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.

Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM. Henderson SJ, et al. Among authors: old jm. Hemoglobin. 2016;40(2):75-84. doi: 10.3109/03630269.2015.1113990. Epub 2015 Dec 4. Hemoglobin. 2016. PMID: 26635043 Review.

9

A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK.

Khalil MSM, Timbs AT, Henderson SJ, Schuh A, El-Khawanky MM, Old JM. Khalil MSM, et al. Among authors: old jm. Hemoglobin. 2020 May;44(3):195-200. doi: 10.1080/03630269.2020.1783288. Epub 2020 Jun 29. Hemoglobin. 2020. PMID: 32597250

10

Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or HBA1: c.-24C>G (or HBA2) Variants.

Khalil MSM, Timbs AT, Henderson SJ, Schuh A, Old JM. Khalil MSM, et al. Among authors: old jm. Hemoglobin. 2020 Sep;44(5):364-367. doi: 10.1080/03630269.2020.1817755. Epub 2020 Sep 14. Hemoglobin. 2020. PMID: 32924661

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