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Year | Number of Results |
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1986 | 1 |
2001 | 1 |
2018 | 1 |
2024 | 0 |
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Late onset hyperornithinemia-hyperammonemia-homocitrullinuria syndrome - how web searching by the family solved unexplained unconsciousness: a case report.
J Med Case Rep. 2018 Sep 23;12(1):274. doi: 10.1186/s13256-018-1794-9.
J Med Case Rep. 2018.
PMID: 30243302
Free PMC article.
BACKGROUND: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a rare inherited urea cycle disorder, can remain undiagnosed for decades and suddenly turn into an acute life-threatening state. Adult presentation of hyperornithinemia- …
BACKGROUND: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a rare inherited urea cycle disorder, c …
Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria).
Hommes FA, Roesel RA, Metoki K, Hartlage PL, Dyken PR.
Hommes FA, et al.
Neuropediatrics. 1986 Feb;17(1):48-52. doi: 10.1055/s-2008-1052499.
Neuropediatrics. 1986.
PMID: 3960284
A patient with the hyperornithinemia, hyperammonemia, homocitrullinuria syndrome is described. ...
A patient with the hyperornithinemia, hyperammonemia, homocitrullinuria syndrome is described. ...
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Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.
Salvi S, Santorelli FM, Bertini E, Boldrini R, Meli C, Donati A, Burlina AB, Rizzo C, Di Capua M, Fariello G, Dionisi-Vici C.
Salvi S, et al.
Neurology. 2001 Sep 11;57(5):911-4. doi: 10.1212/wnl.57.5.911.
Neurology. 2001.
PMID: 11552031
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