Author:
Michotte A.,De Meirleir L.,Lissens W.,Denis R.,Wayenberg J. L.,Liebaers I.,Brucher J. M.
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine
Reference15 articles.
1. Blass JP (1979) Disorders of pyruvate metabolism. Neurology 29:280?286
2. Brown GK, Haan EA, Kirby DM, Scholem RD, Wraith JE, Rogers JG, Danks DM (1988) ?Cerebral? lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis. Eur J Pediatr 147:10?14
3. Brown GK, Brown RM, Scholem RD, Kirby DM, Dahl HHM (1989) The clinical and biochemical spectrum of pyruvate dehydrogenase deficiency. Ann NY Acad Sci 573:360?368
4. Chow CW, Anderson RM, Kenney GCT (1987) Neuropathology in cerebral lactic acidosis. Acta Neuropathol (Berl) 74:393?396
5. Dahl HHM, Maragos C, Brown RM, Hansen LL, Brown GK (1990) Pyruvate dehydrogenase deficiency caused by a deletion of a 7-bp repeat sequence in the E1? gene. Am J Hum Genet 47:286?293
Cited by
36 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献