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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 2
1986 1
1989 3
1993 2
1994 3
1995 1
1996 2
1997 1
2000 2
2001 1
2002 4
2003 2
2004 4
2005 2
2006 6
2007 3
2008 2
2009 3
2010 2
2011 5
2012 7
2013 7
2014 3
2015 5
2016 9
2017 6
2018 5
2019 3
2020 3
2021 4
2022 6
2023 3
2024 2

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101 results

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Page 1
A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia.
Cappellini MD, Viprakasit V, Taher AT, Georgiev P, Kuo KHM, Coates T, Voskaridou E, Liew HK, Pazgal-Kobrowski I, Forni GL, Perrotta S, Khelif A, Lal A, Kattamis A, Vlachaki E, Origa R, Aydinok Y, Bejaoui M, Ho PJ, Chew LP, Bee PC, Lim SM, Lu MY, Tantiworawit A, Ganeva P, Gercheva L, Shah F, Neufeld EJ, Thompson A, Laadem A, Shetty JK, Zou J, Zhang J, Miteva D, Zinger T, Linde PG, Sherman ML, Hermine O, Porter J, Piga A; BELIEVE Investigators. Cappellini MD, et al. Among authors: khelif a. N Engl J Med. 2020 Mar 26;382(13):1219-1231. doi: 10.1056/NEJMoa1910182. N Engl J Med. 2020. PMID: 32212518 Clinical Trial.
REACH: A programme for improving care in haemophilia.
Goga Y, Boukari R, Bensadok M, El Khorassani M, Khelif A, Al Rawas A, Alkasim F, Shaheen NM, Negrier C. Goga Y, et al. Among authors: khelif a. Haemophilia. 2019 May;25(3):e211-e215. doi: 10.1111/hae.13726. Epub 2019 Mar 19. Haemophilia. 2019. PMID: 30888109 No abstract available.
Evidence of a broadband gap in a phononic crystal strip.
Coffy E, Euphrasie S, Addouche M, Vairac P, Khelif A. Coffy E, et al. Among authors: khelif a. Ultrasonics. 2017 Jul;78:51-56. doi: 10.1016/j.ultras.2017.03.003. Epub 2017 Mar 6. Ultrasonics. 2017. PMID: 28319820
Multiple myeloma following essential thrombocythemia.
Ben Youssef Y, Gmidène A, Bouabid Z, Bouallegui S, Sriha B, Zaier M, Sennana H, Khelif A. Ben Youssef Y, et al. Among authors: khelif a. Ann Biol Clin (Paris). 2013 Jul-Aug;71(4):457-60. doi: 10.1684/abc.2013.0856. Ann Biol Clin (Paris). 2013. PMID: 23906574 Free article. Review.
Molecular genetic diagnosis of Tunisian Glanzmann thrombasthenia patients reveals a common nonsense mutation in the ITGA2B gene that seems to be specific for the studied population.
Aloui C, Chakroun T, Granados V, Jemni-Yacoub S, Fagan J, Khelif A, Kahloul N, Hammami S, Chkioua L, Barlier C, Cognasse F, Laradi S, Garraud O. Aloui C, et al. Among authors: khelif a. Blood Coagul Fibrinolysis. 2018 Dec;29(8):689-696. doi: 10.1097/MBC.0000000000000779. Blood Coagul Fibrinolysis. 2018. PMID: 30325339
101 results