Pathophysiology of maple syrup urine disease: Focus on the neurotoxic role of the accumulated branched-chain amino acids and branched-chain α-keto acids - ScienceDirect
Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes - ScienceDirect
Maple Syrup Urine Disease (MSUD) - The Medical Biochemistry Page
Maple syrup urine disease symptoms, causes, diagnosis & diet treatment
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Maple Syrup Urine Disease (Chapter 24) - Progressive Brain Disorders in Childhood
Maple syrup urine disease: mechanisms and management | TACG
Pathophysiology of maple syrup urine disease: Focus on the neurotoxic role of the accumulated branched-chain amino acids and branched-chain α-keto acids - ScienceDirect
PPT - Maple Syrup Urine Disease (MSUD) By Jenny Morrison (836445) PowerPoint Presentation - ID:334267
Maple Syrup Urine Disease and Other Disorders of Branched-Chain Amino Acid Catabolism - YouTube
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Maple Syrup Urine Disease | Pathogenesis, Signs & Symptoms, Subtypes, Diagnosis and Treatment - YouTube
Maple syrup urine disease symptoms - MEDizzy
Maple Syrup Urine Disease - an overview | ScienceDirect Topics
Maple Syrup Urine Disease - Amino Acid Metabolism Disorders - Biochemistry for Medicine
Cureus | Maple Syrup Urine Disease Masquerading as Urea Cycle Disorder: A Tale of Two Clinical Mimics
Maple Syrup Urine Disease - GeneReviews® - NCBI Bookshelf
Maple Syrup Urine Disease (MSUD) — New England Consortium of Metabolic Programs
MSUD (maple syrup urine disease) – newbornscreening.info
MAPLE SYRUP - LEARNING BIOCHEMISTRY
Disorders of Amino Acid Metabolism | Concise Medical Knowledge
Maple syrup urine disease by Jimcale Xamari
Maple Syrup Urine Disease (MSUD): Treatment, Nutritional Therapy
IJMS | Free Full-Text | Brain Branched-Chain Amino Acids in Maple Syrup Urine Disease: Implications for Neurological Disorders
Maple Syrup Urine Disease (MSUD) – Decode Genomics
