Hind Ahmed

A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features

Diane D. Shao, Rachel Straussberg, Hind Ahmed et al. · Genetics in Medicine · 2021 · 27 citations · Full text

Long-term effectiveness of carglumic acid in patients with propionic acidemia (PA) and methylmalonic acidemia (MMA): a randomized clinical trial

Majid Alfadhel, Marwan Nashabat, Mohammed Saleh et al. · Orphanet Journal of Rare Diseases · 2021 · 27 citations · Full text

Evaluation of long-term effectiveness of the use of carglumic acid in patients with propionic acidemia (PA) or methylmalonic acidemia (MMA): study protocol for a randomized controlled trial

Marwan Nashabat, Abdulrahman Obaid, Fuad Al Mutairi et al. · BMC Pediatrics · 2019 · 19 citations · Full text

Bi-allelic <i>ACBD6</i> variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

Rauan Kaiyrzhanov, Abolfazl Rad, Sheng‐Jia Lin et al. · Brain · 2023 · 15 citations · Full text

Brain Development, Genetics, Motor Development +23

Antimicrobial and Antioxidant Activities and Phytochemical Analysis of Rosmarinus officinalis L. Pod and Thymus vulgaris L. Leaf Ethanolic Extracts on Escherichia coli Urinary Isolates

Amel Ahmed Alrasheed, Ayat Ahmed Alrasheid, Wafaa Mohamed Abdalla et al. · International Journal of Microbiology · 2023 · 10 citations · Full text