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

Year Number of Results
1987 1
1991 1
1992 1
1994 3
1995 1
1998 4
1999 1
2001 1
2002 1
2010 1
2013 1
2014 2
2022 0
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17 results
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Page 1
Evolution of muscle specific proteins in Werdnig-Hoffman's disease.
Soussi-Yanicostas N, Ben Hamida C, Bejaoui K, Hentati F, Ben Hamida M, Butler-Browne GS. Soussi-Yanicostas N, et al. Among authors: bejaoui k. J Neurol Sci. 1992 May;109(1):111-20. doi: 10.1016/0022-510x(92)90103-r. J Neurol Sci. 1992. PMID: 1387678
Niemann Pick C: first case in a Canadian Nakoda Nation child.
Khan A, Curtis C, Sarnat HB, Pinto-Rojas A, Bejaoui K, Wei XC, Casey R. Khan A, et al. Among authors: bejaoui k. Can J Neurol Sci. 2014 Jul;41(4):518-21. doi: 10.1017/s0317167100018606. Can J Neurol Sci. 2014. PMID: 24878481 No abstract available.
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy.
Liu J, Aoki M, Illa I, Wu C, Fardeau M, Angelini C, Serrano C, Urtizberea JA, Hentati F, Hamida MB, Bohlega S, Culper EJ, Amato AA, Bossie K, Oeltjen J, Bejaoui K, McKenna-Yasek D, Hosler BA, Schurr E, Arahata K, de Jong PJ, Brown RH Jr. Liu J, et al. Among authors: bejaoui k. Nat Genet. 1998 Sep;20(1):31-6. doi: 10.1038/1682. Nat Genet. 1998. PMID: 9731526
17 results