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Mitochondrial disorders
Citations 91-92 of 92 total displayed.
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Past content
(since Mar 2001):
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- BRIEF COMMUNICATIONS
Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletions
- C. Kornblum, R. Broicher, E. Walther, P. Seibel, H. Reichmann, T. Klockgether, C. Herberhold, and R. Schröder
Neurology 2001; 56: 1409-1412.
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- BRIEF COMMUNICATIONS
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome
- R. Carrozzo, A. Tessa, M.E. Vázquez–Memije, F. Piemonte, C. Patrono, A. Malandrini, C. Dionisi–Vici, L. Vilarinho, M. Villanova, H. Schägger, A. Federico, E. Bertini, and F.M. Santorelli
Neurology 2001; 56: 687-690.
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