Khelifa H - Search Results

1

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development.

Rjiba K, Mougou-Zerelli S, Hamida IH, Saad G, Khadija B, Jelloul A, Slimani W, Hasni Y, Dimassi S, Khelifa HB, Sallem A, Kammoun M, Abdallah HH, Gribaa M, Bignon-Topalovic J, Chelly S, Khairi H, Bibi M, Kacem M, Saad A, Bashamboo A, McElreavey K. Rjiba K, et al. Among authors: khelifa hb. Reprod Biol Endocrinol. 2023 Jan 11;21(1):2. doi: 10.1186/s12958-022-01045-7. Reprod Biol Endocrinol. 2023. PMID: 36631813 Free PMC article.

2

Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis.

Rjiba K, Slimani W, Gaddas M, Hassine IH, Jelloul A, Khelifa HB, El Amri F, Zaouali M, Mcelreavey K, Saad A, Mougou-Zerelli S. Rjiba K, et al. Among authors: khelifa hb. J Clin Res Pediatr Endocrinol. 2023 Feb 27;15(1):25-34. doi: 10.4274/jcrpe.galenos.2022.2022-3-15. Epub 2022 Aug 19. J Clin Res Pediatr Endocrinol. 2023. PMID: 35984215 Free PMC article.

3

Effect of Conducting, Semi-Conducting and Insulating Nanoparticles on AC Breakdown Voltage and Partial Discharge Activity of Synthetic Ester: A Statistical Analysis.

Khelifa H, Beroual A, Vagnon E. Khelifa H, et al. Nanomaterials (Basel). 2022 Jun 19;12(12):2105. doi: 10.3390/nano12122105. Nanomaterials (Basel). 2022. PMID: 35745444 Free PMC article.

4

Healing of Diabetic Neuroischemic Foot Wounds With vs Without Wound-Targeted Revascularization: Preliminary Observations From an 8-Year Prospective Dual-Center Registry.

Alexandrescu VA, Brochier S, Limgba A, Balthazar S, Khelifa H, De Vreese P, Azdad K, Nodit M, Pottier M, Van Espen D, Sinatra T. Alexandrescu VA, et al. Among authors: khelifa h. J Endovasc Ther. 2020 Feb;27(1):20-30. doi: 10.1177/1526602819885131. Epub 2019 Nov 11. J Endovasc Ther. 2020. PMID: 31709886

5

Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization.

Slimani W, Ben Khelifa H, Dimassi S, Chioukh FZ, Jelloul A, Kammoun M, Hannachi H, Bouslah S, Jammali N, Sanlaville D, Saad A, Mougou-Zerelli S. Slimani W, et al. Among authors: ben khelifa h. Mol Cytogenet. 2019 Feb 8;12:5. doi: 10.1186/s13039-019-0414-8. eCollection 2019. Mol Cytogenet. 2019. PMID: 30774715 Free PMC article.

6

Genomic Microarray in Intellectual Disability: The Usefulness of Existing Systems in the Interpretation of Copy Number Variation.

Ben Khelifa H, Soyah N, Labalme A, Guilbert H, Sanlaville D, Saad A, Mougou-Zerelli S. Ben Khelifa H, et al. J Pediatr Genet. 2017 Jun;6(2):84-91. doi: 10.1055/s-0036-1588027. Epub 2016 Sep 8. J Pediatr Genet. 2017. PMID: 28496995 Free PMC article.

7

Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

Khelifa HB, Kammoun M, Hannachi H, Soyah N, Hammami S, Elghezal H, Sanlaville D, Saad A, Mougou-Zerelli S. Khelifa HB, et al. J Pediatr Genet. 2015 Dec;4(4):187-93. doi: 10.1055/s-0035-1565269. Epub 2015 Oct 14. J Pediatr Genet. 2015. PMID: 27617130 Free PMC article.

8

[When diagnostic imaging is misleading: a case of subacute liver failure].

Khelifa H, Seivert M, Colard A, Brichant JF, Boveroux P. Khelifa H, et al. Rev Med Liege. 2015 Jul-Aug;70(7-8):374-7. Rev Med Liege. 2015. PMID: 26376564 Free article. French.

9

Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.

Jellouli NK, Hadj Salem I, Ellouz E, Kamoun Z, kamoun F, tlili A, Kaabachi N, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation study. Jellouli NK, et al. J Hum Genet. 2014 Apr;59(4):216-22. doi: 10.1038/jhg.2014.4. Epub 2014 Feb 27. J Hum Genet. 2014. PMID: 24573090

10

Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation.

Ben Khelifa H, Soyah N, Ben-Abdallah-Bouhjar I, Gritly R, Sanlaville D, Elghezal H, Saad A, Mougou-Zerelli S. Ben Khelifa H, et al. Gene. 2013 Sep 25;527(2):578-83. doi: 10.1016/j.gene.2013.06.018. Epub 2013 Jun 18. Gene. 2013. PMID: 23791652

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