Arginase deficiency presenting as cerebral palsy.

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作者信息

Scheuerle A E, McVie R, Beaudet A L, Shapira S K

机构信息

Institute for Molecular Genetics, Baylor College of Medicine, Houston, TX 77030.

出版信息

Pediatrics. 1993 May;91(5):995-6.

PMID:8474825

Abstract

摘要

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相似文献

Arginase deficiency presenting as cerebral palsy.

Pediatrics. 1993 May;91(5):995-6.

Clinical features and neurologic progression of hyperargininemia.

Pediatr Neurol. 2012 Jun;46(6):369-74. doi: 10.1016/j.pediatrneurol.2012.03.016.

Arginase deficiency with new phenotype and a novel mutation: contemporary summary.

Pediatr Neurol. 2012 Oct;47(4):263-9. doi: 10.1016/j.pediatrneurol.2012.06.012.

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Prenat Diagn. 2004 Nov;24(11):857-60. doi: 10.1002/pd.1000.

"Cerebral Palsy" in a Patient With Arginase Deficiency.

Semin Pediatr Neurol. 2018 Jul;26:110-114. doi: 10.1016/j.spen.2017.03.016. Epub 2017 Apr 1.

Delay and imbalance in milestones as diagnostic indicators for cerebral palsy.

Indian Pediatr. 1969 Oct;6(10):675-9.

Argininemia presenting with progressive spastic diplegia.

Pediatr Neurol. 2011 Mar;44(3):218-20. doi: 10.1016/j.pediatrneurol.2010.11.003.

Contribution of EEG to the detection of cerebral palsy.

Arch Ital Pediatr Pueric. 1967 May-Jun;25(3):232-6.

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Med Sestra. 1982 Sep;41(9):9-12.

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Arch Dis Child. 2001 Nov;85(5):356-60. doi: 10.1136/adc.85.5.356.

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Front Neurol. 2020 Oct 29;11:569996. doi: 10.3389/fneur.2020.569996. eCollection 2020.

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RNA Biol. 2018;15(7):914-922. doi: 10.1080/15476286.2018.1475178. Epub 2018 Jul 24.

Orphanet J Rare Dis. 2012 May 29;7:32. doi: 10.1186/1750-1172-7-32.

Arginase deficiency presenting with convulsions.

J Inherit Metab Dis. 1994;17(2):254. doi: 10.1007/BF00711633.

Molecular basis of phenotypic variation in patients with argininemia.

Hum Genet. 1995 Sep;96(3):255-60. doi: 10.1007/BF00210403.