Hyperornithinemia–hyperammonemia–homocitrullinuria syndrome with stroke-like imaging presentation: Clinical, biochemical and molecular analysis
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference20 articles.
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2. Hyperammonemia–hyperornithinemia–homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients;Lemay;J Pediatr,1992
3. Acute hemiparesis as the presenting sign in a heterozygote for ornithine transcarbamylase deficiency;de Grauw;Neuropediatrics,1990
4. Metabolic stroke in carbamyl phosphate synthetase deficiency;Sperl;Neuropediatrics,1997
5. Neurological manifestations of organic acid disorders;Hoffmann;Eur J Pediatr,1994
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1. Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings;Metabolic Brain Disease;2024-06-04
2. Clinical and radiological description of 120 pediatric stroke‐like episodes;European Journal of Neurology;2023-05-10
3. Late onset hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, presenting as recurrent metabolic encephalopathy, A case report;Annals of Medicine & Surgery;2022-12
4. Stroke-like Episodes in Inherited Neurometabolic Disorders;Metabolites;2022-09-30
5. Impact of Hemorrhagic Stroke on Molar Bite Force: A Prospective Study;Prague Medical Report;2022
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