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Systemic Primary Carnitine Deficiency Presenting With Substantia Nigra and Basal Ganglia Injury: A Case Report Saito 2025 JIMD Reports Wiley Online Library Carnitine Deficiency: What You Need to Know The Medical Biochemistry Page Frontiers Case report: Mitochondrial trifunctional protein deficiency caused by HADHB gene mutation (c.1175C>T) characterized by higher brain dysfunction followed by neuropathy, presented gadolinium enhancement on brain imaging in an adult patient Effect of l carnitine supplementation on muscle cramps induced by stroke: A case report ScienceDirect MR Neuroimaging in Pediatric Inborn Errors of Metabolism PMC
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