(Q39916939)
Statements
1 reference
Mitochondrial myopathy with multisystem abnormalities and normal ocular movements (English)
J. G. McLeod
W. de C. Baker
C. D. Shorey
1 January 1975
1 reference
1 reference
24
1 reference
1
1 reference
39-52
1 reference
15
271
Morphologic features of hypermetabolic mitochondrial disease (English)
Afifi
1972
1
495
Myopathy associated with abnormal lipid metabolism in skeletal muscle (English)
Bradley
1969
79
221
The histographic analysis of human muscle biopsies with regard to fiber type, Part 1 (Adult male and female) (English)
Brooke
1969
126
81
Myopathies avec anomalies mitochondriales localisées aux fibres de type I (English)
Castaigne
1972
12
68
“Megaconial” mitochondria observed in a case of chronic polymyositis (English)
Chou
1969
18
388
Familial myopathy with abnormal muscle mitochondria (English)
D'Agostino
1968
114
169
Etude au microscope électronique des lésions musculaires d'atrophie neurogène par atteinte de la corne antérieure (English)
De Recondo
1966
29
170
Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria (English)
Di Mauro
1973
0 references
18
654
Ophthalmoplegia plus (English)
Drachman
1968
212
1551
Reversal of the ATP-ase reaction in muscle fibres by EDTA (English)
Drews
1966
13
919
Rapid examination of muscle tissue (English)
Engel
1963
184
1851
Enzymatic activities of human skeletal muscle mitochondria: a tool in clinical metabolic research (English)
Ernster
1959
51
619
Mitochondrial myopathy (English)
Fisher
1969
42
169
A generalized disorder of nervous system, skeletal muscle, and heart resembling Refsum's disease and Hurler's syndrome, Part 2 (Ultrastructure) (English)
Gonatas
1967
16
343
Familial “mitochondrial” myopathy (English)
Hudgson
1972
30
519
Myopathy with abnormal structure and function of muscle mitochondria (English)
Hulsmann
1967
29
162
Mitochondria-lipid-glycogen (MLG) disease of muscle (English)
Jerusalem
1973
19
133
The Kearns-Shy syndrome (English)
Karpati
1973
0 references
60
280
Retinitis pigmentosa, external opthalmoplegia and complete heart block (English)
Kearns
1958
17
87
Myopathie distale et congénitale, avec hypertrophie des mollets (English)
Lapresle
1972
68
789
Myopathy and succinylcholine sensitivity (English)
Lessell
1969
41
1776
A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: A correlated clinical, biochemical and morphological study (English)
Luft
1962
33
111
Steroid myopathy complicating McArdle's disease (English)
Mastaglia
1970
96
215
Atypical muscle mitochondria in oculoskeletal myopathy (English)
Morgan-Hughes
1973
14
574
Hypothyroid myopathy (English)
Norris
1966
26
193
Oculocraniosomatic neuromuscular disease with “ragged-red” fibers (English)
Olson
1972
3
170
Factors affecting activity of adenosine triphosphatase and other phosphatases as measured by histochemical techniques (English)
Padykula
1965
26
475
Myopathy with atypical mitochondria in Type I skeletal muscle fibers (English)
Price
1967
17
208
The use of lead acetate at high pH as an electron opaque stain in electron microscopy (English)
Reynolds
1963
0 references
19
37
Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissue (English)
Schneck
1973
17
666
Giant mitochondria in human muscle with inclusions (English)
Shafiq
1967
89
133
Two childhood myopathies with abnormal mitochondria, Part I (Megaconial myopathy), Part 2 (Pleoconial myopathy) (English)
1966
42
163
A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome, Part 1 (Clinical, pathologic, and biochemical characteristics) (English)
1967
22
259
A new mitochondrial myopathy in a patient with salt craving (English)
Spiro
1970
90
577
Skeletal muscle disease with abnormal mitochondria (English)
Van Wijngaarden
1967
153
439
Elektronenmikroskopische Befunde bei 3 Fällen von chronisch progressiver okulärer Muskeldystrophie (English)
Zintz
1967
Identifiers
1 reference
1 reference