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Reham Khalaf-Nazzal
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Hippocampal development–Old and new findings
R Khalaf-Nazzal, F Francis
Neuroscience 248, 225-242, 2013
1212013
New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum
N Bahi-Buisson, I Souville, FJ Fourniol, A Toussaint, CA Moores, ...
Brain 136 (1), 223-244, 2013
1172013
Structural Basis of the Oncogenic Interaction of Phosphatase PRL-1 with the Magnesium Transporter CNNM2*♦
P Giménez-Mascarell, I Oyenarte, S Hardy, T Breiderhoff, M Stuiver, ...
Journal of Biological Chemistry 292 (3), 786-801, 2017
642017
Early born neurons are abnormally positioned in the doublecortin knockout hippocampus
R Khalaf-Nazzal, MA Stouffer, R Olaso, L Muresan, A Roumegous, ...
Human molecular genetics 26 (1), 90-108, 2017
142017
Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse
S Hamelin, B Pouyatos, R Khalaf-Nazzal, T Chabrol, F Francis, O David, ...
Neurobiology of Disease 69, 156-168, 2014
122014
Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice
R Khalaf-Nazzal, E Bruel-Jungerman, JP Rio, J Bureau, T Irinopoulou, ...
PloS one 8 (9), e72622, 2013
102013
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission
J Fasham, AK Huebner, L Liebmann, R Khalaf-Nazzal, R Maroofian, ...
Brain 146 (11), 4547-4561, 2023
52023
Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency
ELBRKN Siying Lin, James Fasham, Fida’ Al-Hijawi, Nouar Qutob, Adam Gunning ...
European Journal of Human Genetics, 2021
52021
Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia
R Khalaf-Nazzal, J Fasham, N Ubeyratna, DJ Evans, JS Leslie, TT Warner, ...
Brain Sciences 11 (5), 614, 2021
52021
Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene
I Dweikat, R Khalaf-Nazzal
Frontiers in Genetics 13, 1004598, 2022
42022
Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder
R Khalaf-Nazzal, J Fasham, KA Inskeep, LE Blizzard, JS Leslie, ...
The American Journal of Human Genetics 109 (11), 2068-2079, 2022
42022
Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families
R Khalaf-Nazzal, I Dweikat, M Maree, M Alawneh, M Barahmeh, ...
Brain and Development 44 (7), 454-461, 2022
32022
Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells
MA Stouffer, R Khalaf-Nazzal, C Cifuentes-Diaz, G Albertini, E Bandet, ...
Neurobiology of Disease 168, 105702, 2022
22022
Phenotypic and Genetic Heterogeneity Linked to the Magnesium Transport Mediator CNNM2
PGHLMTMC Dweikat, Imad & Khalaf, Reham & Giménez, Paula & IM, Dweikat ...
Conference: 2nd International Conference on Educational Neuroscience, 5 Mar …, 2017
2017
Structural Basis of the Oncogenic Interaction of Phosphatase PRL-1 with the Magnesium Transporter CNNM2
AL Pey, J Ereño-Orbea, R Khalaf-Nazzal, D Müller, ML Tremblay, ...
2017
cDepartment of Pediatric Nephrology, Charité Universitäts medizin, Berlin, 13353 Berlin, Germany.
P Giménez-Mascarella, I Oyenartea, S Hardyb, T Breiderhoffc, M Stuivere, ...
2016
A distinct phenotype of childhood leukodystrophy presenting as absence seizure
IM Dweikat, N Damsah, R Khalaf
Journal of Pediatric Neurosciences 9 (1), 63-65, 2014
2014
Organelle and Cellular Abnormalities Associated with Hippocampal
R Khalaf-Nazzal, E Bruel-Jungerman, JP Rio, J Bureau, T Irinopoulou
2013
HMG Advance Access published October 30, 2013
Y Saillour, L Broix, E Bruel-Jungerman, N Lebrun, G Muraca, J Rucci, ...
2013
Ultrastructural, morphological and molecular characterization of heterotopic cells in the hippocampus in epileptic Dcx knockout (KO) mice
R Khalaf-Nazzal
Université Pierre et Marie Curie-Paris VI, 2012
2012
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Articles 1–20