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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 2
1984 2
1985 1
1988 1
1989 1
1992 1
1994 1
1996 1
1997 1
1998 2
2000 1
2002 1
2004 1
2021 1
2024 0

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17 results

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Page 1
Effects of hyperammonaemia on brain function.
Butterworth RF. Butterworth RF. J Inherit Metab Dis. 1998;21 Suppl 1:6-20. doi: 10.1023/a:1005393104494. J Inherit Metab Dis. 1998. PMID: 9686341 Review.
Neuropathological studies reveal Alzheimer type II astrocytosis in the adult hyperammonaemic patient, whereas hyperammonaemia in the infant resulting from congenital urea cycle disorders or Reye syndrome is accompanied by cerebral atrophy, neuronal loss and c …
Neuropathological studies reveal Alzheimer type II astrocytosis in the adult hyperammonaemic patient, whereas hyperammonaemia in the infant …
Reye's syndrome with cortical laminar necrosis: MRI.
Kinoshita T, Takahashi S, Ishii K, Higano S, Matsumoto K, Sakamoto K, Haginoya K, Iinuma K. Kinoshita T, et al. Neuroradiology. 1996 Apr;38(3):269-72. doi: 10.1007/BF00596545. Neuroradiology. 1996. PMID: 8741200
Serial MRI findings are described in two patients with Reye's syndrome, demonstrating diffuse cortical and white matter changes. ...MRI also displayed delayed white matter changes with cerebral atrophy....
Serial MRI findings are described in two patients with Reye's syndrome, demonstrating diffuse cortical and white matter change …
Neuropathologic features, including pontine schwannosis, in a four-year survivor of probable Reye's syndrome with secondary Mobius syndrome.
Manz HJ, Cochran W. Manz HJ, et al. Childs Brain. 1984;11(2):126-34. doi: 10.1159/000120168. Childs Brain. 1984. PMID: 6723427
Frequent seizures and loss of motor, language, and intellectual skills necessitated care in an institution for the physically and mentally handicapped for 4 years after diagnosis of presumed Reye's syndrome in a 10-month-old boy. M obius syndrome was diagnose …
Frequent seizures and loss of motor, language, and intellectual skills necessitated care in an institution for the physically and mentally h …
Pontocerebellar hypoplasia type 2 and Reye-like syndrome.
Sans-Fitó A, Campistol-Plana J, Mas-Salguero MJ, Póo-Argüelles P, Fernández-Alvarez E. Sans-Fitó A, et al. J Child Neurol. 2002 Feb;17(2):132-4. doi: 10.1177/088307380201700208. J Child Neurol. 2002. PMID: 11952074
Pontocerebellar hypoplasia is an autosomal recessive syndrome with onset during the fetal period. Two subtypes of pontocerebellar hypoplasia have been described on the basis of clinical and neuropathologic criteria. ...Cranial magnetic resonance imaging revealed pontocereb …
Pontocerebellar hypoplasia is an autosomal recessive syndrome with onset during the fetal period. Two subtypes of pontocerebellar hyp …
Single-photon emission CT and MR findings in Kluver-Bucy syndrome after Reye syndrome.
Ozawa H, Sasaki M, Sugai K, Hashimoto T, Matsuda H, Takashima S, Uno A, Okawa T. Ozawa H, et al. AJNR Am J Neuroradiol. 1997 Mar;18(3):540-2. AJNR Am J Neuroradiol. 1997. PMID: 9090419 Free PMC article.
We present the MR and single-photon emission CT findings in a 3-year-old patient in whom Kluver-Bucy syndrome developed after Reye syndrome. MR images showed diffuse brain atrophy, which was predominant in the temporal lobes, and single-photon emission …
We present the MR and single-photon emission CT findings in a 3-year-old patient in whom Kluver-Bucy syndrome developed after Reye …
An update of concepts of essential amino acids.
Visek WJ. Visek WJ. Annu Rev Nutr. 1984;4:137-55. doi: 10.1146/annurev.nu.04.070184.001033. Annu Rev Nutr. 1984. PMID: 6380536 Review. No abstract available.
[Neuropathology of Reye's syndrome].
Kuchna I, Kulerski M, Róg-Marczuk J. Kuchna I, et al. Neuropatol Pol. 1988;26(4):547-54. Neuropatol Pol. 1988. PMID: 3253618 Polish. No abstract available.
NBAS deficiency due to biallelic c.2809C > G variant presenting with recurrent acute liver failure with severe hyperammonemia, acquired microcephaly and progressive brain atrophy.
Lipiński P, Greczan M, Piekutowska-Abramczuk D, Jurkiewicz E, Bakuła A, Socha P, Jankowska I, Rokicki D, Tylki-Szymańska A. Lipiński P, et al. Metab Brain Dis. 2021 Oct;36(7):2169-2172. doi: 10.1007/s11011-021-00827-z. Epub 2021 Aug 24. Metab Brain Dis. 2021. PMID: 34427841 Free PMC article.
Since then, some patients with NBAS deficiency presenting with neurologic features, including a motor delay, intellectual disability, muscular hypotonia and a mild brain atrophy, have been reported. Here, we describe a case of pediatric patient diagnosed with NBAS deficien …
Since then, some patients with NBAS deficiency presenting with neurologic features, including a motor delay, intellectual disability, muscul …
17 results