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1.
Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder.
Am J Hum Genet
; 109(11): 2068-2079, 2022 11 03.
Article
in English
| MEDLINE | ID: mdl-36283405
2.
TECPR2-related hereditary sensory and autonomic neuropathy in two siblings from Palestine.
Am J Med Genet A
; 194(7): e63579, 2024 Jul.
Article
in English
| MEDLINE | ID: mdl-38436550
3.
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission.
Brain
; 146(11): 4547-4561, 2023 11 02.
Article
in English
| MEDLINE | ID: mdl-37459438
4.
Early born neurons are abnormally positioned in the doublecortin knockout hippocampus.
Hum Mol Genet
; 26(1): 90-108, 2017 01 01.
Article
in English
| MEDLINE | ID: mdl-28007902
5.
Structural Basis of the Oncogenic Interaction of Phosphatase PRL-1 with the Magnesium Transporter CNNM2.
J Biol Chem
; 292(3): 786-801, 2017 01 20.
Article
in English
| MEDLINE | ID: mdl-27899452
6.
Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse.
Neurobiol Dis
; 69: 156-68, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24874545
7.
New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.
Brain
; 136(Pt 1): 223-44, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-23365099
8.
Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene.
Front Genet
; 13: 1004598, 2022.
Article
in English
| MEDLINE | ID: mdl-36506307
9.
Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families.
Brain Dev
; 44(7): 454-461, 2022 Aug.
Article
in English
| MEDLINE | ID: mdl-35440380
10.
Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia.
Brain Sci
; 11(5)2021 May 11.
Article
in English
| MEDLINE | ID: mdl-34064836
11.
Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency.
Eur J Hum Genet
; 29(10): 1570-1576, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34012134
12.
Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice.
PLoS One
; 8(9): e72622, 2013.
Article
in English
| MEDLINE | ID: mdl-24023755
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