(Q39421136)
Statements
1 reference
Myopathies with abnormal mitochondria. A clinical, histological, and electrophysiological study (English)
2 references
1 January 1977
1 reference
1 reference
55
1 reference
1
1 reference
57-75
1 reference
1 reference
1 reference
1 reference
89
569
Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with core in the muscle fibres (English)
Bethlem
1966
1
495
Myopathy associated with abnormal lipid metabolism in skeletal muscle (English)
Bradley
1969
19
221
The histographic analysis of human muscle biopsies with regard to fiber types. I. Adult male and female (English)
Brooke
1969
21
58
Contraction times and fiber types in neurogenic paresis (English)
Buehthal
1971
30
295
Anomalies mitochondriales à repartition particulière observèes au cours d'une dystrophie musculaire à debut pelvien (English)
Carrier
1974
18
388
Familial myopathy with abnormal muscle mitochondria (English)
D'Agostino
1968
114
169
Etude au microscope électronique des lesions musculaires d'atrophie neurogene par atteinte de la corne anterieure (observées dans huit cas de sclerose laterale amyotrophique) (English)
Recondo
1966
27
217
Luft's disease. Further biochemical and ultrastructural studies in the second case (English)
DiMauro
1976
28
432
Central core disease of muscle with focal wasting (English)
Dubovitz
1965
0 references
13
919
Rapid examination of muscle tissue: An improved trichrome method for rapid diagnosis of muscle biopsy fresh frozen section (English)
Engel
1963
9
585
Improved localization of phosphorylase by the use of polyvinyl pyrrolidone and high substrate concentration (English)
Eränko
1961
274
535
Nemaline myopathy. The origin of nemaline structures (English)
Gonatas
1966
4
753
The cytochemical localization of oxidative enzymes. II. Pyridine nucleotide-linked dehydrogenases (English)
Hess
1958
10
120
A reliable staining method for semi-thin sections in experimental neuroanatomy (English)
Holländer
1968
16
343
Familial “mitochondrial” myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. Part I. Clinical, electrophysiological and pathological findings (English)
Hudgson
1972
24
1033
Familial progressive external ophthalmoplegia and ragged-red fibers (English)
Iannaccone
1974
29
162
Mitochondria-Lipid-Glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy (English)
Jerusalem
1973
49
547
Late onset myopathy with rod-like particles (English)
Kamieniecka
1973
19
133
The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin (English)
Karpati
1973
41
1776
A case of severe hypermetabolism of mitochondrial respiratory control: A correlated clinical, biochemical and morphological study (English)
Luft
1962
96
215
Atypical muscle mitochondria in oculoskeletal myopathy (English)
Morgan-Hughes
1973
48
1
Nemaline myopathy. A histopathological and histochemical study (English)
Nienhuis
1957
14
574
Hypothyroid myopathy. Clinical, electromyographical and ultrastructural observations (English)
Norris
1966
27
79
Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria (English)
Okamura
1976
5
515
Intracellular localization of dehydrogenase system using monotetrazolium salts and metal chelation of their formazans (English)
Pearcc
1957
26
475
Myopathy with atypical mitochondria in type 1 skeletal muscle fibers (English)
Price
1967
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
42
163
A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome, Part I. (Clinical, pathologic and biochemical characteristics) (English)
1967
97
665
Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria (English)
Tamura
1974
Identifiers
1 reference
1 reference