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A 27-Year Old Man with Rapidly Progressive Coma
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The Acquired Metabolic Disorders of the Nervous System, Hepatic Stupor and Coma (Hepatic, or Portal-Systemic Encephalopathy)
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Clinicopathologic Conference, Noncirrhotic hyperammonemia after Roux-en-Y Gastric Bypass
NEJM 389:1221-1230, Case 30-2023, 2023
Risk Factors of Hyperammonemia in Patients with Epilepsy Under Valproic Acid Therapy
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Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014
A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012
Acute Hyperammonemic Encephalopathy in Adults: Imaging Findings
AJNR 32:413-418, U-King-Im,J.M.,et al, 2010
Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993
Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984
Transient Hyperammonemia in the Preterm Infant:Neurologic Aspects
Neurol 31:767-770, Ellison,P.,et al, 1981
Idiopathic Hyperammonemia Associated with Cerebral arteriovenous Malformation
Arch Neurol 37:111-112, Michaelson,P.S., 1980
Reye's Syndrome in the Adult Patient
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