User menu

The Mitochondrial Disorders - Pathogenesis and Etiological Classification

Bibliographic reference Tassin, S. ; Brucher, Jean-Marie. The Mitochondrial Disorders - Pathogenesis and Etiological Classification. In: Neuropathology and Applied Neurobiology, Vol. 8, no. 4, p. 251-263 (1982)
Permanent URL http://hdl.handle.net/2078.1/57280
  1. Ägquist Karl-Axel, Sjöström Michael, Intermittent Claudication and Muscle Fiber Fine Structure: Morphometric Data on Mitochondrial Volumes, 10.3109/01913128009140552
  2. BINDOFF L., Journal of the Neurological Sciences, 39, 1 (1978)
  3. BRUCHER J.M., Mitochondria and Muscular Diseases, 199 (1981)
  4. BRUCHER J.M., Zentral-blatt fur allgemeine Pathologie und Pathologische Anatomie, 125, 564 (1981)
  5. Donato S. D., Cornelio F., Balestrini M. R., Bertagnolio B., Peluchetti D., Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency, 10.1212/wnl.28.11.1110
  6. MAURO S., Handbook of Clinical Neurology, Vol. 41, Diseases of Muscles, part II, 175 (1979)
  7. DiMauro S., Mendell J. R., Sahenk Z., Bachman D., Scarpa A., Scofield R. M., Reiner C., Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency, 10.1212/wnl.30.8.795
  8. Di Mauro Salvatore, Trevisan Carlo, Hays Arthur, Disorders of lipid metabolism in muscle, 10.1002/mus.880030502
  9. Drachman David A., Ophthalmoplegia Plus : The Neurodegenerative Disorders Associated With Progressive External Ophthalmoplegia, 10.1001/archneur.1968.00470360076008
  10. V. DUBOWITZ, and M.H. BROOKE (1973 ) Muscle Biopsy: a Modern Approach. Vol. 2 in the series: Major Problems in Neurology , pp.419 -422 . Saunders, London.
  11. ENGEL A.G, Mayo Clinic Proceedings, 41, 785 (1966)
  12. ENGEL A.G., Mayo Clinic Proceedings, 43, 233 (1968)
  13. FARDEAU M., Muscle Diseases. Proceedings of the International Congress on Muscle Diseases, Milan, 98 (1970)
  14. GARCIN R., Revue. neurologique, 115, 295 (1966)
  15. GODET-GUILLAIN J., Muscle Diseases. Proceedings of the International Congress on Muscle Diseases, Milan, 512 (1970)
  16. Hanzlíková V., Schiaffino S., Mitochondrial changes in ischemic skeletal muscle, 10.1016/s0022-5320(77)80048-8
  17. Heffner R.R., Barron S.A., The early effects of ischemia upon skeletal muscle mitochondria, 10.1016/0022-510x(78)90137-5
  18. Hudgson P., Bradley W.G., Jenkison M., Familial “mitochondrial” myopathy, 10.1016/0022-510x(72)90197-9
  19. Jerusalem Felix, Mitochondria-Lipid-Glycogen (MLG) Disease of Muscle : A Morphologically Regressive Congenital Myopathy, 10.1001/archneur.1973.00490270044007
  20. Kark R. A. P., Rodriguez-Budelli M., Pyruvate dehydrogenase deficiency in spinocerebellar degenerations, 10.1212/wnl.29.1.126
  21. Karpati G., Carpenter S., Melmed C., Eisen A.A., Experimental ischemic myopathy, 10.1016/0022-510x(74)90148-8
  22. E.C. LATERRE, C. BERMILS, S. TASSIN, and J.M. BRUCHER (1981 ) Bilateral muscle hypertrophy of lower limbs after removal of herniated intervertebral L4-L5 disc. Clinical, electrophysiological evaluation and histological findings in nerve and muscle biopsy. Meeting of the Association of British Neurologists and the Belgian Society of Neurology, York, April 1981, p.16 (Abstract).
  23. LUFT R., Journal of Clinical Investigation, 41, 1776 (1962)
  24. Melmed Calvin, Karpati George, Carpenter Stirling, Experimental mitochondrial myopathy produced by in vivo uncoupling of oxidative phosphorylation, 10.1016/0022-510x(75)90204-x
  25. MORGAN-HUGHES J. A., DARVENIZA P., KAHN S. N., LANDON D. N., SHERRATT R. M., LAND J. M., CLARK J. B., A MITOCHONDRIAL MYOPATHY CHARACTERIZED BY A DEFICIENCY IN REDUCIBLE CYTOCHROME b, 10.1093/brain/100.4.617
  26. Morgan-Hughes J.A., Darveniza P., Landon D.N., Land J.M., Clark J.B., A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity, 10.1016/0022-510x(79)90071-6
  27. Olson William, Oculocraniosomatic Neuromuscular Disease With "Ragged-Red" Fibers : Histochemical and Ultrastructural Changes in Limb Muscles of a Group of Patients With Idiopathic Progressive External Ophthalmoplegia, 10.1001/archneur.1972.00490090019001
  28. PENN A.S., Handbook of Clinical Neurology, Vol. 41, Diseases of Muscles, part II, 259 (1979)
  29. RESKE-NIELSEN EDITH, LOU HANS C., LOWES MARTIN, PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA : Evidence for a Generalised Mitochondrial Disease with a Defect in Pyruvate Metabolism, 10.1111/j.1755-3768.1976.tb01285.x
  30. ROUSSEAU J.J., Acta neurologica belgica, 79, 435 (1979)
  31. Sahgal V., Subramani V., Hughes R., Shah A., Singh H., On the pathogenesis of mitochondrial myopathies : An experimental study, 10.1007/bf00690841
  32. Schiffer D., Palmucci L., Bertolotto A., Monga G., Mitochondrial abnormalities of late motor neuron degeneration following poliomyelitis and other neurogenic muscular atrophies, 10.1007/bf00313051
  33. Schotland D. L., DiMauro S., Bonilla E., Scarpa A., Lee C.-P., Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply, 10.1001/archneur.1976.00500070017003
  34. SHAPIRA Y., Israel Journal of Medical Sciences, 13, 161 (1977)
  35. SJOSTROM M., Ultrastructural Pathology, 1, 309 (1980)
  36. SLUGA E., Wiener Klinische Wochenschrift, 79, 917 (1969)
  37. Spiro A. J., Moore C. L., Prineas J. W., Strasberg P. M., Rapin I., A Cytochrome-Related Inherited Disorder of the Nervous System and Muscle, 10.1001/archneur.1970.00480260009002
  38. Spiro A. J., Prineas J. W., Moore C. L., A New Mitochondrial Myopathy in a Patient With Salt Craving, 10.1001/archneur.1970.00480210069009
  39. SULAIMAN W.R., Journal of Neurology, Neurosurgery and Psychiatry, 37, 1236 (1974)
  40. TARLOW M.J., Archives of Disease in Childhood, 48, 489 (1973)
  41. TASSIN S., Louvain Medical, 99, 137 (1980)
  42. TASSIN S., Neuropathology and Applied Neurobiology, 6, 337 (1980)
  43. VAN BIERVLIET J. P. G. M., BRUINVIS L., KETTING D., DE BREE P. K., DER HEIDEN C. VAN, WADMAN S. K., WILLEMS J. L., BOOKELMAN H., HAELST U. VAN, MONNENS L. A. H., Hereditary Mitochondrial Myopathy with Lactic Acidemia, A DeToni-Fanconi-Debr?? Syndrome, and a Defective Respiratory Chain in Voluntary Striated Muscles : , 10.1203/00006450-197711100-00005
  44. van WIJNGAARDEN G. K., BETHLEM J., MEIJER A. E. F. H., HÜLSMANN W. CH., FELTKAMP CONSTANCE A., SKELETAL MUSCLE DISEASE WITH ABNORMAL MITOCHONDRIA, 10.1093/brain/90.3.577
  45. WALTER G.F., Mitochondria and Muscular Diseases, 107 (1981)
  46. Walter G. F., Tassin S., Brucher J. M., Familial Mitochondrial Myopathies, Experimental and Clinical Neuropathology (1981) ISBN:9783540104490 p.283-286, 10.1007/978-3-642-81553-9_82
  47. Worsfold M., Park Dorothy C., Pennington R.J., Familial “mitochondrial” myopathy, 10.1016/0022-510x(73)90090-7