• (<em>R</em>,<em>R</em>)-1,12-Dimethylspermine can mitigate abnormal spermidine accumulation in Snyder-Robinson syndrome
• (R,R)-1,12-Dimethylspermine can mitigate abnormal spermidine accumulation in Snyder-Robinson syndrome
• Author Correction: Modeling Snyder-Robinson Syndrome in multipotent stromal cells reveals impaired mitochondrial function as a potential cause for deficient osteogenesis
• Development of a Redox-Sensitive Spermine Prodrug for the Potential Treatment of Snyder Robinson Syndrome
• Difluoromethylornithine rebalances aberrant polyamine ratios in Snyder-Robinson syndrome
• Difluoromethylornithine rebalances aberrant polyamine ratios in Snyder-Robinson syndrome: mechanism of action and therapeutic potential
• Digestive involvement in a severe form of Snyder-Robinson syndrome: Possible expansion of the phenotype
• Effects of Spermine Synthase Deficiency in Mesenchymal Stromal Cells Are Rescued by Upstream Inhibition of Ornithine Decarboxylase
• Efficacy and Safety of NVX-CoV2373 in Adults in the United States and Mexico
• Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine
• Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase
• Final Report of a Trial of Intensive versus Standard Blood-Pressure Control
• Impaired polyamine metabolism causes behavioral and neuroanatomical defects in a mouse model of Snyder-Robinson syndrome
• Impaired polyamine metabolism causes behavioral and neuroanatomical defects in a novel mouse model of Snyder-Robinson Syndrome
• Maternal mosaicism for a missense variant in the <em>SMS</em> gene that causes Snyder-Robinson syndrome
• Maternal mosaicism for a missense variant in the SMS gene that causes Snyder-Robinson syndrome
• Modeling Snyder-Robinson Syndrome in multipotent stromal cells reveals impaired mitochondrial function as a potential cause for deficient osteogenesis
• Novel Hemizygous Missense Variant of Spermine Synthase (<em>SMS</em>) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy
• Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy
• Phenylbutyrate modulates polyamine acetylase and ameliorates Snyder-Robinson syndrome in a Drosophila model and patient cells
• Preventing amyotrophic lateral sclerosis: insights from pre-symptomatic neurodegenerative diseases
• Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
• Rebalancing polyamine levels to treat Snyder-Robinson syndrome
• Reduction of spermine synthase enhances autophagy to suppress Tau accumulation
• Snyder-Robinson Syndrome
• Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: a novel SMS gene variant
• Snyder-Robinson syndrome: differential diagnosis of osteogenesis imperfecta
• Spermine synthase (<em>SMS</em>) serves as a prognostic biomarker in head and neck squamous cell carcinoma: a bioinformatics analysis
• Structural Insights into the Mechanisms Underlying Polyaminopathies
• Two New Cases of Bachmann-Bupp Syndrome Identified through the International Center for Polyamine Disorders
• Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with Snyder-Robinson Syndrome