「MYOPATHY」の共起表現(1語右で並び替え) - Weblio英語共起表現検索


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Weblio 辞書 > 英和辞典・和英辞典 > MYOPATHYの意味・解説 > MYOPATHYに関連した共起表現

「MYOPATHY」の共起表現一覧(1語右で並び替え)

該当件数 : 28



apparently a common cause of exercise-induced myopathy and probably the most common cause of metabol
The infantile form causes severe myopathy and leads to death in infancy or early childh
city is hepatic (abnormal liver enzymes), and myopathy and rarely rhabdomyolysis have been reported.
ombination with statins, increase the risk of myopathy and rhabdomyolysis.
Serum creatine kinase is elevated in Bethlem myopathy, as there is ongoing muscle cell death.
eek QUASH studies) was terminated due to some myopathy cases in patients.
ns, the sympathetic nervous system; laryngeal myopathy, central lesions of the nervous system, laryn
eases, acromegaly, denervation atrophy, lipid myopathy, chronic obstructive pulmonary disease, centr
It may lead to myopathy, exercise intolerance and rhabdomyolysis asso
Bethlem myopathy has an autosomal dominant pattern of inherita
Brody myopathy is a genetic disease.
Congenital myopathy is a term for any muscle disorder present at
Bethlem myopathy is an extremely rare disorder, with fewer tha
Distal muscular dystrophy (or distal myopathy) is a group of disorders characterized by ons
Desmin-related myofibrillar myopathy is a subgroup of the myofibrillar myopathy di
elop abnormal, hypertrophic lungs and cardiac myopathy, leading to a reduction in life span.
Patients with Bethlem myopathy may expect a normal life span and continued m
hy, but also presents itself in centronuclear myopathy, myotonic dystrophy and various other conditi
One source includes nemaline myopathy, myotubular myopathy, central core myopathy,
in an aquarium, presumably dying from capture myopathy or stress .
Niacin also is proved to increase the risk of myopathy or rhabdomyolysis.
decompensation, and later in life by skeletal myopathy or cardiomyopathy.
protracted progressive course associated with myopathy, recurrent rhabdomyolysis, and sensorimotor a
strophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.
The deficiency was the first metabolic myopathy to be recognized, when Dr. McArdle described
l muscular dystrophy (also called nutritional myopathy, White muscle disease) is a muscular disease
X-linked myopathy with postural muscle atrophy (XMPMA)
k S, Acar A, Cevikbas U. A family of visceral myopathy; with pseudo-obstruction, megaduodenum, Barre
                                                                                                    


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