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单词 duchenne muscular dystrophy
释义

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Duchenne muscular dystrophy
Used attributively and in the possessive (esp. as Duchenne muscular dystrophy) to designate the severe form of muscular dystrophy described by him, formerly called pseudohypertrophic muscular dystrophy; also in combination as Duchenne-type adj., and elliptical as Duchenne.
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the world > health and disease > ill health > a disease > diseases of tissue > disorders affecting muscles > [adjective] > other muscular disorders
myalgic1860
Duchenne1870
parelectronomic1877
contractural1928
amyotonic1961
the world > health and disease > ill health > a disease > diseases of tissue > disorders affecting muscles > [noun] > degeneration or decay > disease characterized by > types of
Duchenne1870
myosclerotic paralysis1873
1870 W. B. Kesteven in Jrnl. Mental Sci. 16 46 I believe we should herein only be doing justice if in future we shortened the lengthy title of ‘Pseudo-Hypertrophic Muscular Paralysis of Duchenne’ into the brief, though not very scientific, form—‘Duchenne's Paralysis’.
1896 T. C. Allbutt et al. Syst. Med. I. 184 Duchenne's paralysis, in which pseudo-hypertrophy occurs.
1936 Arch. Neurol. & Psychiatry (Chicago) 36 1296 Minkowski and Sidler, from studies in Switzerland, concluded that in the Duchenne type inheritance of the disease occurs as a recessive mendelian character.
1954 Brain 77 185 In our opinion the group should be entitled simply ‘Duchenne type muscular dystrophy’. This group will include the traditional ‘pseudohypertrophic muscular dystrophy’.
1980 Neurology 30 206/1 Detection of Duchenne carriers is usually based on serum creatine kinase (CK) activity.
1982 T. M. Devlin Textbk. Biochem. xxi. 1005 A number of components in the sarcoplasm of skeletal muscle are found to be present in lower than normal levels in patients with Duchenne's muscular dystrophy.
1991 Conquest Feb. 180 In 1987..the gene responsible for muscular dystrophy of the Duchenne type was finally isolated, localised and characterised in the Xp21 region of the..X chromosome.
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