Author:
van der Knaap Marjo S.,Valk Jacob
Publisher
Springer Berlin Heidelberg
Reference72 articles.
1. Adickes ED, Buehler BA, Sanger WG (1986) Familial lethal sleep apnea. Hum Genet 73: 39–43
2. Anzil AP, Weindl A, Struppler A (1981) Ultrastructure of a cerebral white matter lesion in a 41-year-old man with Leighs encephalomyelopathy ( LEM ). Acta Neuropathol (Berl) Suppl V II: 233–238
3. Arts WFM, Scholte HR, Loonen MCB, Przyrembel H, Fernandes J, Trijbels JMF, Luyt-Houwen IEM (1987) Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy. J Neurol Sci 77: 103–115
4. Awata H, Endo F, Tanoue A, Kitano A, Matsuda I (1994) Characterization of a point mutation in the pyruvate dehydrogenase E1, gene from two boys with primary lactic acidaemia. J Inherited Metab Dis 17: 189–195
5. Bianco F, Floris R, Pozzessere G, Rizzo PA (1987) Subacute necrotizing encephalomyelopathy (Leighs disease): clinical correlations with computerized tomography in the diagnosis of the juvenile and adult forms. Acta Neurol Scand 75: 214–217