• A case of hypersarcosinaemia
• A patient with sarcosinaemia
• A Rapid Method for the Detection of Sarcosine Using SPIONs/Au/CS/SOX/NPs for Prostate Cancer Sensing
• A report of two families with sarcosinaemia in Hong Kong and revisiting the pathogenetic potential of hypersarcosinaemia
• A Spanish family with sarcosinemia
• A young adult with sarcosinemia. No benefit from long duration treatment with memantine
• Chemically induced acute model of sarcosinemia in wistar rats
• Clinical and cellular studies of sarcosinemia
• Cloning and mapping of the cDNA for human sarcosine dehydrogenase, a flavoenzyme defective in patients with sarcosinemia
• Considerations on sarco-leukosis; lymphosarcomatous cell leukemia
• Discovery of Tricyclic Clerodane Diterpenes as Sarco/Endoplasmic Reticulum Ca(2+)-ATPase Inhibitors and Structure-Activity Relationships
• Elevated serum creatinine without discernible kidney disease
• Endogenous formaldehyde is a memory-related molecule in mice and humans
• Erythro-sarco-leukemia
• Esophagogastrointestinal leiomyo(sarco)mas
• Evaluation of Oxidative Stress Parameters and Energy Metabolism in Cerebral Cortex of Rats Subjected to Sarcosine Administration
• Inborn errors of imino acid metabolism
• Increased prevalence of hereditary metabolic diseases among native Indians in Manitoba and northwestern Ontario
• Massachusetts Metabolic Disorders Screening Program: III. Sarcosinemia
• Molecular clonging of the human dimethyglycine dehydrogenase-like gene (DMGDHL1) from the sarcosinemia critical region at 9q34
• Molecular cloning and tissue distribution of rat sarcosine dehydrogenase
• Mutation in Smek2 regulating hepatic glucose metabolism causes hypersarcosinemia and hyperhomocysteinemia in rats
• Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia
• Quantitative analysis of sarcosine with special emphasis on biosensors: a review
• Rare neurodevelopmental abnormalities of sarcosinemia may involve glycinergic stimulation of a primed N-methyl-d-aspartate receptor
• sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesis
• Sarcosinaemia in a patient with severe progressive neurological damage and hypertrophic cardiomyopathy
• Sarcosinaemia in a patient with Usher syndrome
• Sarcosinaemia in a retarded, amaurotic child
• Sarcosinemia associated with folate deficiency
• SBF-1 exerts strong anticervical cancer effect through inducing endoplasmic reticulum stress-associated cell death via targeting sarco/endoplasmic reticulum Ca(2+)-ATPase 2
• The mouse mutation sarcosinemia (sar) maps to chromosome 2 in a region homologous to human 9q33-q34