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Frequency of congenital dyserythropoietic anemias in Europe.
Heimpel H, Matuschek A, Ahmed M, Bader-Meunier B, Colita A, Delaunay J, Garcon L, Gilsanz F, Goede J, Högel J, Kohne E, Leichtle R, Munoz J, Perrotta S, Piscopo C, Renella R, Schwarz K, Smolenska-Sym G, Wickramasinghe S, Zanella A, Iolascon A. Heimpel H, et al. Among authors: ahmed m. Eur J Haematol. 2010 Jul;85(1):20-5. Eur J Haematol. 2010. PMID: 20665989
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.
Babbs C, Roberts NA, Sanchez-Pulido L, McGowan SJ, Ahmed MR, Brown JM, Sabry MA; WGS500 Consortium; Bentley DR, McVean GA, Donnelly P, Gileadi O, Ponting CP, Higgs DR, Buckle VJ. Babbs C, et al. Among authors: ahmed mr. Haematologica. 2013 Sep;98(9):1383-7. doi: 10.3324/haematol.2013.089490. Epub 2013 May 28. Haematologica. 2013. PMID: 23716552 Free PMC article.
'Popeye' Sign: A Visual Vignette.
Swarnakar R, Saha A, Sarkar A, Ahmed M. Swarnakar R, et al. Among authors: ahmed m. Am J Phys Med Rehabil. 2024 Dec 9. doi: 10.1097/PHM.0000000000002679. Online ahead of print. Am J Phys Med Rehabil. 2024. PMID: 39787340 No abstract available.
Biomarkers.
Sillau SH, Coughlan CM, Ahmed MM, Nair KV, Araya P, Galbraith MD, Bettcher BM, Espinosa JM, Chial HJ, Epperson N, Boyd TD, Potter H. Sillau SH, et al. Among authors: ahmed mm. Alzheimers Dement. 2024 Dec;20 Suppl 2(Suppl 2):e092726. doi: 10.1002/alz.092726. Alzheimers Dement. 2024. PMID: 39785257 Free PMC article.
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