Amal M. Al Teneiji

Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II.

R. Cohn, M. Moharir, R. Mendoza-Londono, 2017, Molecular genetics and metabolism.

Novel mutation causing propionic acidemia associated with unexplained autoimmune thyrotoxicosis

Nida Sakrani, A. Ibrahim, Jamal Al Jubeh, 2021, Molecular genetics and metabolism reports.

Phenotype, biochemical features, genotype and treatment outcome of pyridoxine-dependent epilepsy

S. Weiss, M. Inbar‐Feigenberg, E. Struys, 2016, Metabolic Brain Disease.

Hereditary orotic aciduria (HOA): A novel uridine-5-monophosphate synthase (UMPS) mutation

S. Sacharow, Amal M. Al Teneiji, A. Al Shamsi, 2021, Molecular genetics and metabolism reports.

BCAP31‐associated encephalopathy and complex movement disorder mimicking mitochondrial encephalopathy

N. Monfared, S. Mercimek-Mahmutoglu, Saleh Albanyan, 2017, American journal of medical genetics. Part A.

Endothelial Dysfunction and the Effect of Arginine and Citrulline Supplementation in Children and Adolescents With Mitochondrial Diseases

A. El-Hattab, K. Al-Thihli, J. Hertecant, 2020, Journal of central nervous system disease.

Progressive Cerebellar Atrophy and a Novel Homozygous Pathogenic DNAJC19 Variant as a Cause of Dilated Cardiomyopathy Ataxia Syndrome.

S. Mital, K. Siriwardena, S. Mercimek-Mahmutoglu, 2016, Pediatric neurology.

Retinal venous tortuosity in a woman hemizygous for MBTPS2 mutation

Arif O. Khan, Amal M. Al Teneiji, 2019, Ophthalmic genetics.

Homozygous and heterozygous retinal phenotypes in families harbouring IMPG2 mutations

Arif O. Khan, Amal M Al Teneiji, Amal M. Al Teneiji, 2019, Ophthalmic genetics.