Neurology · 2006 · 108 citations · 9 references
MedicineNeurosciencePediatricsDevelopmental PediatricsNeonatal HealthNeonatologyCongenital DisordersNeonatal DevelopmentNeonatal Metabolic DisordersNeonatal NeurologyNeonatal NutritionNeurodevelopmental DisordersArginine MetabolismEarly Case DetectionEarly Syndrome DetectionHereditary Neurometabolic DisordersPediatric Neurogenetic DisordersPresymptomatic Diagnosis
Prospective observation in a neonate with guanidinoacetate methyltransferase deficiency (GAMT-D), a severe neurometabolic disorder, revealed increased guanidinoacetate levels at birth. After 14-month treatment with creatine, high-dose ornithine, benzoate, and an arginine-restricted diet, the patient's development is normal and she does not present any symptoms of GAMT-D. The authors' observation indicates that early detection of GAMT-D is possible in the neonatal period, and presymptomatic treatment may prevent its manifestation.
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Andreas Schulze · Molecular and Cellular Biochemistry · 2003 · 189 citations
Andreas Schulze, Friedrich Ebinger, D. Rating et al. · Molecular Genetics and Metabolism · 2001 · 156 citations
Activation of GABAA Receptors by Guanidinoacetate: A Novel Pathophysiological Mechanism
Axel Neu, Henrike Neuhoff, Gerhard Trube et al. · Neurobiology of Disease · 2002 · 125 citations · Full text
Lack of creatine in muscle and brain in an adult with GAMT deficiency
Andreas Schulze, Peter Bachert, H Schlemmer et al. · Annals of Neurology · 2003 · 119 citations
Medicine, Neurology, Neuroscience +15