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Clinical quiz.
Abolghasemi H, Kavehmanesh Z, Matinzadeh ZK, Amid A, Ahmadi M. Abolghasemi H, et al. J Pediatr Gastroenterol Nutr. 2005 Feb;40(2):229, 243. doi: 10.1097/00005176-200502000-00029. J Pediatr Gastroenterol Nutr. 2005. PMID: 15711419 No abstract available.
Factor XIII deficiency in south-east Iran.
Eshghi P, Abolghasemi H, Sanei-Moghaddam E, Anwar R, Jazebi M, Amid A, Ala FA. Eshghi P, et al. Among authors: abolghasemi h. Haemophilia. 2004 Sep;10(5):470-2. doi: 10.1111/j.1365-2516.2004.00951.x. Haemophilia. 2004. PMID: 15357772 No abstract available.
Thalassemia in Iran: epidemiology, prevention, and management.
Abolghasemi H, Amid A, Zeinali S, Radfar MH, Eshghi P, Rahiminejad MS, Ehsani MA, Najmabadi H, Akbari MT, Afrasiabi A, Akhavan-Niaki H, Hoorfar H. Abolghasemi H, et al. J Pediatr Hematol Oncol. 2007 Apr;29(4):233-8. doi: 10.1097/MPH.0b013e3180437e02. J Pediatr Hematol Oncol. 2007. PMID: 17414565
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence.
Barco S, Sollfrank S, Trinchero A, Adenaeuer A, Abolghasemi H, Conti L, Häuser F, Kremer Hovinga JA, Lackner KJ, Loewecke F, Miloni E, Vazifeh Shiran N, Tomao L, Wuillemin WA, Zieger B, Lämmle B, Rossmann H. Barco S, et al. Among authors: abolghasemi h. J Thromb Haemost. 2020 Jul;18(7):1598-1617. doi: 10.1111/jth.14805. Epub 2020 May 15. J Thromb Haemost. 2020. PMID: 32202057 Free article.
Clinical and genetic characteristics of hemoglobin H disease in Iran.
Abolghasemi H, Kamfar S, Azarkeivan A, Karimi M, Keikhaei B, Abolghasemi F, Radfar MH, Eshghi P, Alavi S. Abolghasemi H, et al. Pediatr Hematol Oncol. 2022 Sep;39(6):489-499. doi: 10.1080/08880018.2021.2017529. Epub 2021 Dec 24. Pediatr Hematol Oncol. 2022. PMID: 34951342
94 results