Diana Alasmar

Hajdu Cheney syndrome; A novel NOTCH2 mutation in a Syrian child, and treatment with zolidronic acid: A case report and a literature review of treatments

Afaf Ahmad, H. Deeb, Diana Alasmar, 2021, Annals of medicine and surgery.

Mutation spectrum of phenylketonuria in Syrian population: genotype-phenotype correlation.

Diana Alasmar, Hossam Murad, W. Al-achkar, 2013, Gene.

Gaucher disease in Syrian children: common mutations identification and clinical futures

Diana Alasmar, 2015, Annals of Saudi medicine.

Reversible dilated cardiomyopathy as a complication of adrenal cortex insufficiency: a case report

Diana Alasmar, M. Alkhateeb, M. Alsakkal, 2018, Journal of Medical Case Reports.

Uncertain significance mutation in the POLR3B gene in a Syrian boy with leukodystrophy: a case report

Diana Alasmar, Zulfiqar Hamdan, 2023, Annals of Medicine and Surgery.

Novel mutation in the RAB3GAP1 gene, the first diagnosed Warburg Micro syndrome case in Syria

Diana Alasmar, Rawan Al khudari, Soubhi Tenawi, 2020, Oxford Medical Case Reports.

Documentation of a novel FBP1 gene mutation in the Arabian ethnicity: a case report

Diana Alasmar, Maher Almousa, Mohammad Aljomaa, 2024, Journal of medical case reports.