Khalaf-Nazzal R - Search Results

1

Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice.

Khalaf-Nazzal R, Bruel-Jungerman E, Rio JP, Bureau J, Irinopoulou T, Sumia I, Roumegous A, Martin E, Olaso R, Parras C, Cifuentes-Diaz C, Francis F. Khalaf-Nazzal R, et al. PLoS One. 2013 Sep 2;8(9):e72622. doi: 10.1371/journal.pone.0072622. eCollection 2013. PLoS One. 2013. PMID: 24023755 Free PMC article.

2

Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells.

Stouffer MA, Khalaf-Nazzal R, Cifuentes-Diaz C, Albertini G, Bandet E, Grannec G, Lavilla V, Deleuze JF, Olaso R, Nosten-Bertrand M, Francis F. Stouffer MA, et al. Among authors: khalaf nazzal r. Neurobiol Dis. 2022 Jun 15;168:105702. doi: 10.1016/j.nbd.2022.105702. Epub 2022 Mar 24. Neurobiol Dis. 2022. PMID: 35339680 Free article.

3

Early born neurons are abnormally positioned in the doublecortin knockout hippocampus.

Khalaf-Nazzal R, Stouffer MA, Olaso R, Muresan L, Roumegous A, Lavilla V, Carpentier W, Moutkine I, Dumont S, Albaud B, Cagnard N, Roest Crollius H, Francis F. Khalaf-Nazzal R, et al. Hum Mol Genet. 2017 Jan 1;26(1):90-108. doi: 10.1093/hmg/ddw370. Hum Mol Genet. 2017. PMID: 28007902

4

Hippocampal development - old and new findings.

Khalaf-Nazzal R, Francis F. Khalaf-Nazzal R, et al. Neuroscience. 2013 Sep 17;248:225-42. doi: 10.1016/j.neuroscience.2013.05.061. Epub 2013 Jun 10. Neuroscience. 2013. PMID: 23756184 Review.

5

Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse.

Hamelin S, Pouyatos B, Khalaf-Nazzal R, Chabrol T, Francis F, David O, Depaulis A. Hamelin S, et al. Neurobiol Dis. 2014 Sep;69:156-68. doi: 10.1016/j.nbd.2014.05.025. Epub 2014 May 27. Neurobiol Dis. 2014. PMID: 24874545

6

New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.

Bahi-Buisson N, Souville I, Fourniol FJ, Toussaint A, Moores CA, Houdusse A, Lemaitre JY, Poirier K, Khalaf-Nazzal R, Hully M, Leger PL, Elie C, Boddaert N, Beldjord C, Chelly J, Francis F; SBH-LIS European Consortium. Bahi-Buisson N, et al. Brain. 2013 Jan;136(Pt 1):223-44. doi: 10.1093/brain/aws323. Brain. 2013. PMID: 23365099 Free PMC article.

7

Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families.

Khalaf-Nazzal R, Dweikat I, Maree M, Alawneh M, Barahmeh M, Doulani RT, Qrareya M, Qadi M, Dudin A. Khalaf-Nazzal R, et al. Brain Dev. 2022 Aug;44(7):454-461. doi: 10.1016/j.braindev.2022.03.009. Epub 2022 Apr 16. Brain Dev. 2022. PMID: 35440380

8

Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia.

Khalaf-Nazzal R, Fasham J, Ubeyratna N, Evans DJ, Leslie JS, Warner TT, Al-Hijawi F, Alshaer S, Baker W, Turnpenny PD, Baple EL, Crosby AH. Khalaf-Nazzal R, et al. Brain Sci. 2021 May 11;11(5):614. doi: 10.3390/brainsci11050614. Brain Sci. 2021. PMID: 34064836 Free PMC article.

9

Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency.

Lin S, Fasham J, Al-Hijawi F, Qutob N, Gunning A, Leslie JS, McGavin L, Ubeyratna N, Baker W, Zeid R, Turnpenny PD, Crosby AH, Baple EL, Khalaf-Nazzal R. Lin S, et al. Among authors: khalaf nazzal r. Eur J Hum Genet. 2021 Oct;29(10):1570-1576. doi: 10.1038/s41431-021-00887-w. Epub 2021 May 20. Eur J Hum Genet. 2021. PMID: 34012134 Free PMC article.

10

TECPR2-related hereditary sensory and autonomic neuropathy in two siblings from Palestine.

Khalaf-Nazzal R, Dweikat I, Ubeyratna N, Fasham J, Alawneh M, Leslie J, Maree M, Gunning A, Zayed DZ, Voutsina N, McGavin L, Sawafta R, Owens M, Baker W, Turnpenny P, Al-Hijawi F, Baple EL, Crosby AH, Rawlins LE. Khalaf-Nazzal R, et al. Am J Med Genet A. 2024 Jul;194(7):e63579. doi: 10.1002/ajmg.a.63579. Epub 2024 Mar 4. Am J Med Genet A. 2024. PMID: 38436550

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