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

Year Number of Results
1976 1
1981 1
1982 1
1983 1
1984 1
1985 1
1992 1
1995 2
1996 1
1997 3
1998 1
1999 3
2000 1
2001 1
2002 1
2006 1
2007 1
2008 1
2009 3
2010 4
2011 1
2012 2
2013 3
2014 1
2015 1
2016 1
2021 1
2024 0

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39 results

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Page 1
Nocturnal epilepsies in adults.
Yaqub BA, Waheed G, Kabiraj MM. Yaqub BA, et al. Among authors: kabiraj mm. Seizure. 1997 Apr;6(2):145-9. doi: 10.1016/s1059-1311(97)80069-6. Seizure. 1997. PMID: 9153728 Free article.
C19orf12 mutation leads to a pallido-pyramidal syndrome.
Kruer MC, Salih MA, Mooney C, Alzahrani J, Elmalik SA, Kabiraj MM, Khan AO, Paudel R, Houlden H, Azzedine H, Alkuraya F. Kruer MC, et al. Among authors: kabiraj mm. Gene. 2014 Mar 10;537(2):352-6. doi: 10.1016/j.gene.2013.11.039. Epub 2013 Dec 17. Gene. 2014. PMID: 24361204 Free PMC article.
Neurosciences quiz. Eyelid fluttering artifact.
Kabiraj M, Al-Salamah A, Al-Janoubi N. Kabiraj M, et al. Neurosciences (Riyadh). 2010 Apr;15(2):134-5. Neurosciences (Riyadh). 2010. PMID: 20672507 No abstract available.
SLC25A22 is a novel gene for migrating partial seizures in infancy.
Poduri A, Heinzen EL, Chitsazzadeh V, Lasorsa FM, Elhosary PC, LaCoursiere CM, Martin E, Yuskaitis CJ, Hill RS, Atabay KD, Barry B, Partlow JN, Bashiri FA, Zeidan RM, Elmalik SA, Kabiraj MM, Kothare S, Stödberg T, McTague A, Kurian MA, Scheffer IE, Barkovich AJ, Palmieri F, Salih MA, Walsh CA. Poduri A, et al. Among authors: kabiraj mm. Ann Neurol. 2013 Dec;74(6):873-82. doi: 10.1002/ana.23998. Ann Neurol. 2013. PMID: 24596948 Free PMC article.
Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.
Tesson C, Nawara M, Salih MA, Rossignol R, Zaki MS, Al Balwi M, Schule R, Mignot C, Obre E, Bouhouche A, Santorelli FM, Durand CM, Oteyza AC, El-Hachimi KH, Al Drees A, Bouslam N, Lamari F, Elmalik SA, Kabiraj MM, Seidahmed MZ, Esteves T, Gaussen M, Monin ML, Gyapay G, Lechner D, Gonzalez M, Depienne C, Mochel F, Lavie J, Schols L, Lacombe D, Yahyaoui M, Al Abdulkareem I, Zuchner S, Yamashita A, Benomar A, Goizet C, Durr A, Gleeson JG, Darios F, Brice A, Stevanin G. Tesson C, et al. Among authors: kabiraj mm. Am J Hum Genet. 2012 Dec 7;91(6):1051-64. doi: 10.1016/j.ajhg.2012.11.001. Epub 2012 Nov 21. Am J Hum Genet. 2012. PMID: 23176821 Free PMC article.
Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes.
Mihaylova V, Müller JS, Vilchez JJ, Salih MA, Kabiraj MM, D'Amico A, Bertini E, Wölfle J, Schreiner F, Kurlemann G, Rasic VM, Siskova D, Colomer J, Herczegfalvi A, Fabriciova K, Weschke B, Scola R, Hoellen F, Schara U, Abicht A, Lochmüller H. Mihaylova V, et al. Among authors: kabiraj mm. Brain. 2008 Mar;131(Pt 3):747-59. doi: 10.1093/brain/awm325. Epub 2008 Jan 7. Brain. 2008. PMID: 18180250
39 results