Kalthoum Graiess-Tlili
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 8 publications
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: November 01, 2020
Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly.
Journal: Journal of medical genetics
Published: June 11, 2020
Neuroimaging manifestations and genetic heterogeneity of Walker-Warburg syndrome in Saudi patients.
Journal: Brain & development
Published: May 26, 2020
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.
Journal: American journal of human genetics
Published: June 04, 2019
Distinct neuroimaging features of DDHD2 gene-related spastic paraplegia, a mimicker of cerebral palsy.
Journal: Archives of disease in childhood
Published: December 26, 2018
Neuroregression, coarse features, and oligosaccharides in urines.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: October 24, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026