「MYOPATHY」の共起表現一覧(1語右で並び替え)
該当件数 : 28件
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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