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

Year Number of Results
1993 1
1995 1
2004 2
2009 2
2010 6
2011 4
2012 1
2013 1
2015 2
2016 1
2017 1
2019 1
2020 1
2021 4
2022 1
2023 3

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27 results

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Page 1
SRD5A3-CDG: 3D structure modeling, clinical spectrum, and computer-based dysmorphic facial recognition.
Ben Ayed I, Ouarda W, Frikha F, Kammoun F, Souissi A, Ben Said M, Bouzid A, Elloumi I, Hamdani TM, Gharbi N, Baklouti N, Guirat M, Mejdoub F, Kharrat N, Boujelbene I, Abdelhedi F, Belguith N, Keskes L, Gibriel AA, Kamoun H, Triki C, Alimi AM, Masmoudi S. Ben Ayed I, et al. Among authors: kammoun f. Am J Med Genet A. 2021 Apr;185(4):1081-1090. doi: 10.1002/ajmg.a.62065. Epub 2021 Jan 6. Am J Med Genet A. 2021. PMID: 33403770
[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.
A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome.
Fendri-Kriaa N, Boujilbene S, Kammoun F, Mkaouar-Rebai E, Ben Mahmoud A, Hsairi I, Rebai A, Triki C, Fakhfakh F. Fendri-Kriaa N, et al. Among authors: kammoun f. Biochem Biophys Res Commun. 2011 May 20;408(4):654-7. doi: 10.1016/j.bbrc.2011.04.079. Epub 2011 Apr 21. Biochem Biophys Res Commun. 2011. PMID: 21531204
27 results