Visual pathways evaluation in Kearns Sayre syndrome: a diffusion tensor imaging study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Neurology (clinical),Radiology, Nuclear Medicine and imaging
Link
http://link.springer.com/content/pdf/10.1007/s00234-019-02302-0.pdf
Reference25 articles.
1. Kearns TP, Sayre GP (1958) Retinitis pigmentosa, external ophthalmoplegia, and complete heart block: unusual syndrome with histologic study in one of two cases. AMA Arch Ophthalmol 60:280–289. https://doi.org/10.1001/archopht.1958.00940080296016
2. Yamashita S, Nishino I, Nonaka I, Goto Y-I (2008) Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions. J Hum Genet 53:598–606. https://doi.org/10.1007/s10038-008-0289-8
3. Davis R, Sue C (2011) The genetics of mitochondrial disease. Semin Neurol 31:519–530. https://doi.org/10.1055/s-0031-1299790
4. Hourani RG, Barada WM, Al-Kutoubi AM, Hourani MH (2006) Atypical MRI findings in Kearns-Sayre syndrome: T2 radial stripes. Neuropediatrics 37(2):110–113. https://doi.org/10.1055/s-2006-924226
5. Van der Knaap M, Valk J (2005) Myelination and myelin disorders, 3rd edn. Springer, New York, pp 231–220
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