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Myoclonus status revealing COVID 19 infection.
Seizure. 2023 Jan;104:12-14. doi: 10.1016/j.seizure.2022.11.010. Epub 2022 Nov 22.
Seizure. 2023.
PMID: 36446232
Free PMC article.
External validations of the ABCD2 score in prediction of stroke risk after transient ischemic attack. A Tunisian hospital-based cohort study.
Nizar D, Amine MM, Aissi M, Machraoui R, Adel S, Khaoula BHA, Blel S, Younes S, Boukef R, Henteti F, Nouira S, Hamdi B, Frih M.
Nizar D, et al. Among authors: blel s.
Int J Neurosci. 2023 Dec;133(11):1218-1223. doi: 10.1080/00207454.2020.1835897. Epub 2023 Jul 19.
Int J Neurosci. 2023.
PMID: 33059508
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[Health insurance in Tunisia, current context and future perspectives].
Blel S.
Blel S.
Tunis Med. 2001 May;79(5):278-84.
Tunis Med. 2001.
PMID: 11515469
French.
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Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C).
Ben Othmane K, Speer MC, Stauffer J, Blel S, Middleton L, Ben Hamida C, Etribi A, Loeb D, Hentati F, Roses AD, et al.
Ben Othmane K, et al. Among authors: blel s.
Am J Hum Genet. 1995 Sep;57(3):732-4.
Am J Hum Genet. 1995.
PMID: 7668303
Free PMC article.
No abstract available.
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Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.
Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM.
Ben Othmane K, et al. Among authors: blel s.
Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625.
Hum Mol Genet. 1993.
PMID: 8268915
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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD, et al.
Ben Othmane K, et al. Among authors: blel s.
Nat Genet. 1992 Dec;2(4):315-7. doi: 10.1038/ng1292-315.
Nat Genet. 1992.
PMID: 1303286
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