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

Year Number of Results
1988 1
1989 2
1990 1
1995 1
1998 1
2003 2
2004 1
2006 2
2007 2
2008 5
2009 9
2010 2
2011 9
2012 7
2013 6
2014 1
2015 12
2016 10
2017 3
2018 7
2019 7
2020 8
2021 6
2022 1
2023 2
2024 2

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97 results

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Page 1
[Richner-Hanhart syndrome].
Zribi H, Souissi A, Azzouz H, Tebib N, Mokni M. Zribi H, et al. Among authors: tebib n. Presse Med. 2016 Feb;45(2):264-5. doi: 10.1016/j.lpm.2015.03.016. Epub 2016 Feb 12. Presse Med. 2016. PMID: 26880079 French. No abstract available.
Une triste histoire qui se répète….
Tebib N. Tebib N. Rev Med Suisse. 2021 Jun 30;17(744-2):1284. Rev Med Suisse. 2021. PMID: 34219427 French. No abstract available.
Souvenons-nous de Gaza.
Tebib N. Tebib N. Rev Med Suisse. 2024 May 22;20(875):1052. doi: 10.53738/REVMED.2024.20.875.1052. Rev Med Suisse. 2024. PMID: 38783678 French. No abstract available.
Distinctive findings in a boy with Simpson-Golabi-Behmel syndrome.
Halayem S, Hamza M, Maazoul F, Ben Turkia H, Touati M, Tebib N, Mrad R, Bouden A. Halayem S, et al. Among authors: tebib n. Am J Med Genet A. 2016 Apr;170A(4):1035-9. doi: 10.1002/ajmg.a.37518. Epub 2015 Dec 22. Am J Med Genet A. 2016. PMID: 26692054 Review.
Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012).
Mellouli F, Mustapha IB, Khaled MB, Besbes H, Ouederni M, Mekki N, Ali MB, Larguèche B, Hachicha M, Sfar T, Gueddiche N, Barsaoui S, Sammoud A, Boussetta K, Becher SB, Meherzi A, Guandoura N, Boughammoura L, Harbi A, Amri F, Bayoudh F, Jaballah NB, Tebib N, Bouaziz A, Mahfoudh A, Aloulou H, Mansour LB, Chabchoub I, Boussoffara R, Chemli J, Bouguila J, Hassayoun S, Hammami S, Habboul Z, Hamzaoui A, Ammar J, Barbouche MR, Bejaoui M. Mellouli F, et al. Among authors: tebib n. J Clin Immunol. 2015 Nov;35(8):745-53. doi: 10.1007/s10875-015-0206-9. Epub 2015 Oct 13. J Clin Immunol. 2015. PMID: 26464197 Review.
Morning specimen is not representative of metabolic control in Tunisian children with phenylketonuria: a repeated cross-sectional study.
Ben Abdelaziz R, Tangour N, Ben Chehida A, Haj Taieb S, Feki M, Azzouz H, Tebib N. Ben Abdelaziz R, et al. Among authors: tebib n. J Pediatr Endocrinol Metab. 2020 Jul 11:/j/jpem.ahead-of-print/jpem-2020-0025/jpem-2020-0025.xml. doi: 10.1515/jpem-2020-0025. Online ahead of print. J Pediatr Endocrinol Metab. 2020. PMID: 32653876 Review.
Consanguinity, endogamy, and genetic disorders in Tunisia.
Ben Halim N, Ben Alaya Bouafif N, Romdhane L, Kefi Ben Atig R, Chouchane I, Bouyacoub Y, Arfa I, Cherif W, Nouira S, Talmoudi F, Lasram K, Hsouna S, Ghazouani W, Azaiez H, El Matri L, Abid A, Tebib N, Ben Dridi MF, Kachboura S, Amouri A, Mokni M, Ben Arab S, Dellagi K, Abdelhak S. Ben Halim N, et al. Among authors: tebib n. J Community Genet. 2013 Apr;4(2):273-84. doi: 10.1007/s12687-012-0128-7. Epub 2012 Dec 4. J Community Genet. 2013. PMID: 23208456 Free PMC article. No abstract available.
97 results