Literature DB >> 7502989

Symmetric lesions of the subthalamic nuclei in mitochondrial encephalopathies: an almost distinctive Mark of Leigh disease with COX deficiency.

M Savoiardo, E Ciceri, L D'Incerti, G Uziel, G Scotti.   

Abstract

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Year:  1995        PMID: 7502989      PMCID: PMC8337772     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


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  6 in total

1.  Leigh syndrome: MRI findings in two children.

Authors:  Al Kartikasalwah; Ngu Lh
Journal:  Biomed Imaging Interv J       Date:  2010-01-01

2.  MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.

Authors:  Laura Farina; Luisa Chiapparini; Graziella Uziel; Marianna Bugiani; Massimo Zeviani; Mario Savoiardo
Journal:  AJNR Am J Neuroradiol       Date:  2002-08       Impact factor: 3.825

Review 3.  Pediatric neurodegenerative white matter processes: leukodystrophies and beyond.

Authors:  Jonathan A Phelan; Lisa H Lowe; Charles M Glasier
Journal:  Pediatr Radiol       Date:  2008-04-30

4.  Radio-imaging for detecting congenitally defective metabolic pathways: A review.

Authors:  Sushil Kachewar; Devidas Kulkarni; Smita Sankaye
Journal:  Australas Med J       Date:  2011-09-30

5.  Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings.

Authors:  Andrea Rossi; Roberta Biancheri; Claudio Bruno; Maja Di Rocco; Angela Calvi; Alice Pessagno; Paolo Tortori-Donati
Journal:  AJNR Am J Neuroradiol       Date:  2003 Jun-Jul       Impact factor: 3.825

6.  A rare mitochondrial disorder: Leigh syndrome--a case report.

Authors:  Dhananjay Y Shrikhande; Piyush Kalakoti; M M Aarif Syed; Kunal Ahya; Gurmeet Singh
Journal:  Ital J Pediatr       Date:  2010-09-15       Impact factor: 2.638

  6 in total

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