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

Year Number of Results
1982 1
1988 2
1989 3
1990 4
1991 3
1992 5
1993 3
1994 2
1997 2
1998 2
1999 2
2000 1
2001 1
2004 2
2005 1
2006 1
2007 2
2008 7
2009 3
2010 2
2011 3
2013 1
2016 3
2017 3
2018 2
2019 4
2020 1
2021 2
2023 1
2024 1

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69 results

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Page 1
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Motta M, Fasano G, Gredy S, Brinkmann J, Bonnard AA, Simsek-Kiper PO, Gulec EY, Essaddam L, Utine GE, Guarnetti Prandi I, Venditti M, Pantaleoni F, Radio FC, Ciolfi A, Petrini S, Consoli F, Vignal C, Hepbasli D, Ullrich M, de Boer E, Vissers LELM, Gritli S, Rossi C, De Luca A, Ben Becher S, Gelb BD, Dallapiccola B, Lauri A, Chillemi G, Schuh K, Cavé H, Zenker M, Tartaglia M. Motta M, et al. Among authors: ben becher s. Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8. Am J Hum Genet. 2021. PMID: 34626534 Free PMC article.
Inherited bisalbuminemia with growth hormone deficiency.
Dabboubi R, Amri Y, Sahli C, Fredj SH, Essaddam L, Zoghlami A, Ben Becher S, Messaoud T. Dabboubi R, et al. Among authors: ben becher s. Clin Chem Lab Med. 2019 Aug 27;57(9):e226-e229. doi: 10.1515/cclm-2018-1133. Clin Chem Lab Med. 2019. PMID: 30763259 No abstract available.
Ben Becher S, Zaafouri M, Bardi I, Ben Jaballah N, Besbes M, Kilani T, Boudhina T. Ben Becher S, et al. Arch Fr Pediatr. 1992 Feb;49(2):109-12. Arch Fr Pediatr. 1992. PMID: 1316109 Review. French.
A rare cause of cyanosis: Congenital methemoglobinemia.
Guedri R, Missaoui N, Essaddam L, Ben Becher S. Guedri R, et al. Among authors: ben becher s. Clin Case Rep. 2021 Jul 10;9(7):e04422. doi: 10.1002/ccr3.4422. eCollection 2021 Jul. Clin Case Rep. 2021. PMID: 34267908 Free PMC article.
Abdominal tuberculosis in children.
Tinsa F, Essaddam L, Fitouri Z, Brini I, Douira W, Ben Becher S, Boussetta K, Bousnina S. Tinsa F, et al. Among authors: ben becher s. J Pediatr Gastroenterol Nutr. 2010 Jun;50(6):634-8. doi: 10.1097/MPG.0b013e3181b6a57b. J Pediatr Gastroenterol Nutr. 2010. PMID: 20386326
[Sydenham's chorea in children].
Ghram N, Allani C, Oudali B, Fitouri Z, Ben Becher S. Ghram N, et al. Among authors: ben becher s. Arch Pediatr. 1999 Oct;6(10):1048-52. doi: 10.1016/s0929-693x(00)86977-8. Arch Pediatr. 1999. PMID: 10544778 French.
[Gaucher's disease in Tunisia (multicenter study)].
Chaabouni M, Aoulou H, Tebib N, Hachicha M, Ben Becher S, Monastiri K, Yacoub M, Sfar T, Elloumi M, Chakroun N, Miled M, Ben Dridi MF. Chaabouni M, et al. Among authors: ben becher s. Rev Med Interne. 2004 Feb;25(2):104-10. doi: 10.1016/s0248-8663(03)00267-4. Rev Med Interne. 2004. PMID: 14744639 French.
[Pediatric Crohn's disease in Tunisia].
Siala N, Benzarti A, Boukthir S, Brini I, Sammoud A, Bousnina S, Ben Becher S, Lakhoua R, Fethi B, Harbi A, Gueddiche N, Sfar T, Hachicha M, Ben Hariz M, Maherzi A. Siala N, et al. Among authors: ben becher s. Tunis Med. 2013 Dec;91(12):715-23. Tunis Med. 2013. PMID: 24458675 French.
Central system nervous tuberculosis in infants.
Tinsa F, Essaddam L, Fitouri Z, Boussetta K, Ben Becher S, Bousnina S. Tinsa F, et al. Among authors: ben becher s. J Child Neurol. 2010 Jan;25(1):102-6. doi: 10.1177/0883073809336129. J Child Neurol. 2010. PMID: 20032518
[The re-emergence of pertussis in Tunisia].
Zouari A, Smaoui H, Njamkepo E, Mnif K, Ben Jaballah N, Bousnina S, Barsaoui S, Sammoud A, Ben Becher S, Guiso N, Kechrid A. Zouari A, et al. Among authors: ben becher s. Med Mal Infect. 2011 Feb;41(2):97-101. doi: 10.1016/j.medmal.2010.11.008. Epub 2011 Jan 6. Med Mal Infect. 2011. PMID: 21215539 French.
69 results