Dergiler / Türk Pediatri Arşivi / 2013 / Cilt: 48 - Sayı: 1

Kaybolan beyaz madde hastalığı; nadir bir olgu

Vanishing white matter leukodystrophy, a rare case report

Sayfa
78–79
Yayın Tarihi
2022-11-05
DOI
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Bu Makaleye Atıf Yap

GÜLER, S., YÜKSEL, A., İŞCAN, A., TATLI, B., IŞIK, İ. (2022). Kaybolan beyaz madde hastalığı; nadir bir olgu. Türk Pediatri Arşivi, Cilt: 48 - Sayı: 1, 78–79. https://ajindex.com/articles/641325

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Kaynakça (2)

  1. Bugiani M, Boor I, Powers JM, Scheper GC, van der Knaap MS. Leukoencephalopathy with vanishing white matter: a review. J Neuropathol Exp Neurol 2010; 69(10): 987-6. 2. van der Knaap MS, Kamphorst W, Barth PG, Kraaijeveld CL, Gut E, Valk J. Phenotypicvariation in leukoencephalopathy with vanishing white matter. Neurology 1998; 51: 540-7
  2. Vermeulen G, Seidl R, Mercimek-Mahmutoglu S, Rotteveel JJ, Scheper GC, van der Knaap MS. Fright is a provoking factor in vanishing white matter disease. Ann Neurol 2005; 57(4): 560-3. 4. van der Knaap MS, Leegwater PA, Könst AA, et al. Mutations in each of the five subunits of translation initiation factor eIF2B can cause leu- koencephalopathy with vanishing white matter. Ann Neurol 2002; 51(2): 264-70. 5. van der Knaap MS, Leegwater PA, van Berkel CG, et al. Arg113His mutation in eIF2Bepsilon as cause of leukoencephalopathy in adults. Neurology 2004; 62(9): 1598-600. 6. van der Knaap MS, van Berkel CG, Herms J, et al. eIF2B-related disor- ders: antenatal onset and involvement of multiple organs. Am J Hum Genet 2003; 73: 1199-207.