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Neutropenia in Barth syndrome: characteristics, risks, and management.
Curr Opin Hematol. 2019 Jan;26(1):6-15. doi: 10.1097/MOH.0000000000000472.
Curr Opin Hematol. 2019.
PMID: 30451719
Free PMC article.
Clinical Trial.
Barth syndrome.
Clarke SL, Bowron A, Gonzalez IL, Groves SJ, Newbury-Ecob R, Clayton N, Martin RP, Tsai-Goodman B, Garratt V, Ashworth M, Bowen VM, McCurdy KR, Damin MK, Spencer CT, Toth MJ, Kelley RI, Steward CG.
Clarke SL, et al. Among authors: mccurdy kr.
Orphanet J Rare Dis. 2013 Feb 12;8:23. doi: 10.1186/1750-1172-8-23.
Orphanet J Rare Dis. 2013.
PMID: 23398819
Free PMC article.
Review.
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Barth Syndrome Foundation: From humble beginnings to becoming an integral partner.
Lontok E, Milligan E, Bowen VM, McCurdy KR.
Lontok E, et al. Among authors: mccurdy kr.
J Inherit Metab Dis. 2022 Jan;45(1):3-6. doi: 10.1002/jimd.12432. Epub 2021 Sep 16.
J Inherit Metab Dis. 2022.
PMID: 34480756
No abstract available.
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Gastritis Cystica Profunda: A Deeper Problem.
McCurdy KR, Parmar K, de Melo SW.
McCurdy KR, et al.
ACG Case Rep J. 2016 Sep 14;3(4):e125. doi: 10.14309/crj.2016.98. eCollection 2016 Aug.
ACG Case Rep J. 2016.
PMID: 27807577
Free PMC article.
No abstract available.
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Creating a global rare disease patient registry linked to a rare diseases biorepository database: Rare Disease-HUB (RD-HUB).
Rubinstein YR, Groft SC, Bartek R, Brown K, Christensen RA, Collier E, Farber A, Farmer J, Ferguson JH, Forrest CB, Lockhart NC, McCurdy KR, Moore H, Pollen GB, Richesson R, Miller VR, Hull S, Vaught J.
Rubinstein YR, et al. Among authors: mccurdy kr.
Contemp Clin Trials. 2010 Sep;31(5):394-404. doi: 10.1016/j.cct.2010.06.007. Epub 2010 Jul 8.
Contemp Clin Trials. 2010.
PMID: 20609392
Free PMC article.
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