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[Use of recombinant factor VII in Glanzmann thrombasthenia: a case report].
Chabchoub Ben Abdallah R, Trabelsi L, Ben Ameur S, Kammoun F, Boukédi A, Ben Salah M, Ben Hlima N, Mahfoudh A. Chabchoub Ben Abdallah R, et al. Among authors: kammoun f. Arch Pediatr. 2010 Jul;17(7):1062-4. doi: 10.1016/j.arcped.2010.04.006. Epub 2010 Jun 8. Arch Pediatr. 2010. PMID: 20570498 French.
[Multiple cerebral cavernomatosis in a 1-year-old child].
Chabbchoub Ben Abdallah R, Kammoun F, Ayedi M, Trabelsi L, Ben Salah M, Ben Hlima N, Mahfoudh A. Chabbchoub Ben Abdallah R, et al. Among authors: kammoun f. Arch Pediatr. 2010 Aug;17(8):1156-8. doi: 10.1016/j.arcped.2010.05.002. Epub 2010 Jun 9. Arch Pediatr. 2010. PMID: 20542671 French.
8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects.
Ben Ayed I, Bouzid A, Kammoun F, Souissi A, Jallouli O, Mallouli S, Guidara S, Loukil S, Aloulou H, Jbeli F, Aouichaoui S, Abid D, Abdelhedi F, Triki C, Kamoun H, Masmoudi S. Ben Ayed I, et al. Among authors: kammoun f. Mol Genet Genomic Med. 2021 Nov;9(11):e1811. doi: 10.1002/mgg3.1811. Epub 2021 Sep 22. Mol Genet Genomic Med. 2021. PMID: 34549899 Free PMC article.
29 results