Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH)-Syndrome
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Pathology and Forensic Medicine
Reference34 articles.
1. Ornithinemia hyperammonemia and homocitrullinuria: A disease associated with mental retardation and possibly caused by defective mitochondrial transport;Fell;Am J Dis Child,1974
2. Hyperornithinemia, hyperamrnonemia and homocitrullinuria associated with decreased carbamylphosphate synthetase I activity;Gatfield;Pediat Res,1975
3. Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia and homocitrullinuria;Haust;Human Pathol,1981
4. Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia and homocitrullinuria syndrome;Haust;Birth Defects: Original Article Series,1987
5. Biochemical analysis of decreased ornithine transport activity in the liver mitochondria from patients with hyperornithinemia hyperammonemia and homocitrullinuria;Inoue;Biochim Biophys Acta,1988
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1. Deterministic Absolute Negative Mobility for Micro- and Submicrometer Particles Induced in a Microfluidic Device;Analytical Chemistry;2016-05-17
2. The hyperornithinemia–hyperammonemia-homocitrullinuria syndrome;Orphanet Journal of Rare Diseases;2015-03-11
3. HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation;Journal of Inherited Metabolic Disease;2006-02
4. Hyperornithinaemia- hyperammonaemia- homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter;Nature Genetics;1999-06
5. Enzymdefekte des Harnstoffzyklus in der Differentialdiagnose der akuten Enzephalopathie im Erwachsenenalter;Der Nervenarzt;1999-02-09
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