Zur ultrastruktur der Myoklonusk�rper
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF00686372.pdf
Reference23 articles.
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2. Edgar, G. W. F.: Progressive myoclonus epilepsy as inborn error of metabolisme comparable to storage disease. Epilepsia (Amst.)4, 120?137 (1963).
3. Harriman, D. G. F., andJ. H. D. Millar: Progressive familial myoclonic epilepsy in 3 families. (Its clinical features and pathological basis). Brain78, 325?349 (1955).
4. van Heykop ten Ham, M. W., andH. de Jager: Progressive myoclonus epilepsy with Lafora bodies. Clinical-pathological features. Epilepsia (Amst.)4, 95?119 (1963).
5. Karnowsky, M. J.: Simple methods for ?staining with lead? at high pH in electron microscopy. J. biophys. biochem. Cytol.11, 729?732 (1961).
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1. Über eine der Myoklonuskörperkrankheit (Morbus Lafora) des Menschen und des Hundes morphologisch ähnliche Speicherkrankheit bei einem Nymphensittich (Nymphicus hollandicus);Zentralblatt für Veterinärmedizin Reihe A;2010-05-13
2. NEUROPATHOLOGICAL STUDIES IN THREE SCANDINAVIAN CASES OF PROGRESSIVE MYOCLONUS EPILEPSY;Acta Neurologica Scandinavica;2009-01-29
3. Lafora Disease: Diagnosis and Carrier Detection;Verhandlungen der Deutschen Gesellschaft für Neurologie;1987
4. Presenile Dementia-A Form of Lafora Disease;Journal of the American Geriatrics Society;1980-05
5. Maladie de lafora;Journal of the Neurological Sciences;1975-08
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