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Publications by JUNKO WATANABE
A Case of Ornithine Transcarbamylase Deficiency With Acute and Late Onset Simulating Reye's Syndrome in an Adult Male.
Kurume Medical Journal
Medicine
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Paternal Transmission and Slow Elimination of Mutant Alleles Associated With Late-Onset Ornithine Transcarbamylase Deficiency in Male Patients
Journal of Human Genetics
Genetics
Intravenous Arginine Dramatically Improved Hyperammonemia in a Patient With Late-Onset Ornithine Transcarbamylase Deficiency.
Tohoku Journal of Experimental Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Reye's Syndrome: Serum Glutamic Oxalacetic Transaminase Isozymes and Ornithine Transcarbamylase Activity
Kurume Medical Journal
Medicine
Family Studies in Ornithine Transcarbamylase Deficiency.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Ornithine Transcarbamylase Deficiency – The Real Cause of “Family Curse”. A Case Report
Russkii Zhunal Detskoi Nevrologii
Child Health
Neurology
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Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency
Archives of Disease in Childhood
Child Health
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Liver Peroxisome Damage During Acute Hepatic Failure in Partial Ornithine Transcarbamylase Deficiency
Pediatric Research
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Acute Extrapyramidal Syndrome in Mild Ornithine Transcarbamylase Deficiency: Metabolic Stroke Involving the Caudate and Putamen Without Metabolic Decompensation
European Journal of Pediatrics
Child Health
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Hiding in Plain Sight: A Case of Ornithine Transcarbamylase Deficiency Unmasked Post-Liver Transplantation
American Journal of Transplantation
Transplantation
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Pharmacology
