H. Al-Dhalaan

发表

Novel Mitochondrial DNA Transversion Mutation in Transfer Ribonucleic Acid for Leucine 2 (CUN) in a Patient With the Clinical Features of MELAS

K. Abu-Amero, P. Ozand, H. Al-Dhalaan, 2006, Journal of child neurology.

Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.

Olfat Al-Harazi, N. Kaya, D. Çolak, 2020, Omics : a journal of integrative biology.

Seizure outcomes after hemispherectomy for drug resistant epilepsy in childhood and adolescence

Faisal Al-Otaibi, H. Al-Dhalaan, Salah Baz, 2019 .

Vanishing white matter in Saudi Arabia.

H. Al-Dhalaan, Mohammad A Al-Muhaizea, Fahad Al-Jofan, 2008, Neurosciences.

A novel X‐linked disorder with developmental delay and autistic features

F. Alkuraya, N. Kaya, D. Çolak, 2012, Annals of neurology.

Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease

N. Kaya, D. Çolak, S. Coskun, 2008, Genetics in Medicine.

Feasibility of Responsive Teaching With Mothers and Young Children With Autism in Saudi Arabia

G. Mahoney, A. Al-odaib, H. Al-Dhalaan, 2018, Journal of Early Intervention.

A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Robert W. Taylor, A. Hellani, K. Abu-Amero, 2009, Journal of medical case reports.

Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways.

N. Kaya, D. Çolak, P. Ozand, 2011, Genomics.