SYNJ1 gene associated with neonatal onset of neurodegenerative disorder and intractable seizure

por Al Zaabi, Nuha, Al Menhali, Noora, Al‐Jasmi, Fatma
Publicado 2017

Alpha‐L‐iduronidase deficiency: A novel mutation resulting in severe early presentation of Mucopolysaccharidosis type I and literature review of the molecular basis

por Al Zaabi, Nuha Nasser, Sirajum, Muneera, Al‐Wawi, Mohd Zaki, Al Suwaiji, Mohammed
Publicado 2022

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

por Al Jasmi, Fatma, Al Zaabi, Nuha, Al-Thihli, Khalid, Al Teneiji, Amal M, Hertecant, Jozef, El-Hattab, Ayman W
Publicado 2020