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Year Number of Results
2005 2
2006 1
2011 1
2012 5
2013 3
2014 3
2015 1
2016 4
2017 2
2018 2
2019 1
2020 1
2021 3
2022 3
2023 3
2024 2

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31 results

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Page 1
[Hematologic abnormalities in infantile visceral leishmaniasis].
Chouchene S, Braham N, Bouatay A, Hizem S, Berriri S, Eljemai A, Boughamoura L, Kortas M. Chouchene S, et al. Among authors: hizem s. Arch Pediatr. 2015 Nov;22(11):1107-11. doi: 10.1016/j.arcped.2015.08.012. Arch Pediatr. 2015. PMID: 26433577 French.
[Platelet satellitism during cutaneous leishmaniasis].
Chouchene S, Braham N, Hizem S, Bouatay A, Abidi B, Dakhli M, Denguezli M, Mahjoub T, Kortas M. Chouchene S, et al. Among authors: hizem s. Ann Biol Clin (Paris). 2014 Nov-Dec;72(6):743-6. doi: 10.1684/abc.2014.1017. Ann Biol Clin (Paris). 2014. PMID: 25486672 Free article. French.
Beckwith-Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature.
Sassi H, Elaribi Y, Jilani H, Rejeb I, Hizem S, Sebai M, Kasdallah N, Bouthour H, Hannachi S, Beygo J, Saad A, Buiting K, H'mida Ben-Brahim D, BenJemaa L. Sassi H, et al. Among authors: hizem s. Mol Genet Genomic Med. 2021 Oct;9(10):e1796. doi: 10.1002/mgg3.1796. Epub 2021 Sep 12. Mol Genet Genomic Med. 2021. PMID: 34510813 Free PMC article. Review.
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities.
Al Kaissi A, Ryabykh S, Nassib N, Bouchoucha S, Benjemaa L, Rejeb I, Hizem S, Kenis V, Grill F, Kircher SG, Shboul M, Ben Chehida F. Al Kaissi A, et al. Among authors: hizem s. Diagnostics (Basel). 2022 Sep 30;12(10):2375. doi: 10.3390/diagnostics12102375. Diagnostics (Basel). 2022. PMID: 36292064 Free PMC article.
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).
Essaddam L, Zitouni O, Kraoua L, Trabelsi M, Sassi H, Kmiha S, Charfi F, El Guiche D, Kebaïli R, Jaballah N, Rjeb M, Zouari N, El Aribi Y, Hizem S, Wannes S, Fkih Romdhane I, Sfar MT, Ben Hamouda H, Hadj Salem R, Khlayfia Z, Khmiss T, Monastiri K, Siala N, Chouchane S, Souaa H, Khochtali I, Mahjoub B, Sfar H, Ben Jemâa L, Abroug S, Boughamoura L, Kamoun I, Kamoun T, Mrad R, Ben Becher S. Essaddam L, et al. Among authors: hizem s. J Pediatr Endocrinol Metab. 2023 Apr 21;36(6):577-583. doi: 10.1515/jpem-2022-0360. Print 2023 Jun 27. J Pediatr Endocrinol Metab. 2023. PMID: 37084413
Genome Tunisia Project: paving the way for precision medicine in North Africa.
Hamdi Y, Trabelsi M, Ghedira K, Boujemaa M, Ben Ayed I, Charfeddine C, Souissi A, Rejeb I, Kammoun Rebai W, Hkimi C, Neifar F, Jandoubi N, Mkaouar R, Chaouch M, Bennour A, Kamoun S, Chaker Masmoudi H, Abid N, Mezghani Khemakhem M; GTCA Consortium; Masmoudi S, Saad A, BenJemaa L, BenKahla A, Boubaker S, Mrad R, Kamoun H, Abdelhak S, Gribaa M, Belguith N, Kharrat N, Hmida D, Rebai A. Hamdi Y, et al. Genome Med. 2024 Aug 27;16(1):104. doi: 10.1186/s13073-024-01365-w. Genome Med. 2024. PMID: 39187811 Free PMC article.
31 results