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Annals of Medicine and Surgery (2012)|June 26, 2023
Guillan-barre syndrome during COVID-19 pandemic: a case series from SyriaIbrahim Labbad, Ibrahim Shammas, Aram Abbas, et al.
Annals of the Rheumatic Diseases|June 1, 2025
Mitochondria-centred metabolomic map of inclusion body myositis: sex-specific alterations in central carbon metabolismElie Naddaf, Ibrahim Shammas, Surendra Dasari, et al.
European Journal of Neurology|April 29, 2025
Increased Risk of Myocardial Infarction in Inclusion Body Myositis: A Non-Concurrent Cohort StudyGrayson Beecher, Sara Muhammad, Ibrahim Shammas, et al.
Cells|April 13, 2026
Reversible Metabolic and Liver Disease in Complex III Deficiency: Novel Variants Expand the Reported UQCRC2-Associated PhenotypeGraeme Preston, Ibrahim Shammas, Filippo Pinto E Vairo, et al.
American Journal of Medical Genetics. Part A|September 26, 2024
Case Report of Friedreich's Ataxia and ALG1 -Related Biochemical Abnormalities in a Patient With Progressive Spastic ParaplegiaAisling Quinlan, Lance Rodan, Elizabeth Barkoudah, et al.
BMC Cancer|August 23, 2025
Epidemiological and clinicopathological characteristics of ovarian cancer in Syria during the war years: a national multicenter retrospective study (2017-2021)Shant Apelian, Alaa Hamdan, Rita Mohammad, et al.
Molecular Genetics and Metabolism|May 4, 2024
ALG13-Congenital Disorder of Glycosylation (ALG13-CDG): Updated clinical and molecular review and clinical management guidelinesRameen Shah, Erik A Eklund, Silvia Radenkovic, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Multilevel impairment of mitochondrial respiration with sex-specific signatures in inclusion body myositisIbrahim Shammas, Hazem Iaali, Jens O Watzlawik, et al.
Frontiers in Genetics|May 21, 2024
Case report: Novel genotype of ALG2-CDG and confirmation of the heptasaccharide glycan (NeuAc-Gal-GlcNAc-Man2-GlcNAc2) as a specific diagnostic biomarkerIvan Martínez Duncker, Denisse Mata-Salgado, Ibrahim Shammas, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
PGM1 deficiency disrupts sarcomere and mitochondrial function in a stem-cell cardiomyocyte modelSilvia Radenkovic, Graeme Preston, Rohit Budhraja, et al.
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