Duchenne muscular dystrophy and glycerol kinase deficiency: a rare contiguous gene syndrome [0.03%]
杜氏肌营养不良伴甘油激酶缺乏症：一种罕见的连续基因综合征
A A Amato
A A Amato
Duchenne muscular dystrophy (DMD), glycerol kinase deficiency (GKD), and adrenal hypoplasia congenita (AHC) can occur together as part of a contiguous gene syndrome located at chromosome Xp21, GKD can manifest with recurrent episodes of vom...
Hidden afterdischarges in slow channel congenital myasthenic syndrome [0.03%]
缓慢通道型先天性重症肌无力中的隐藏后放电现象
R S Bedlack,T E Bertorini,D B Sanders
R S Bedlack
Afterdischarges in motor nerve stimulation studies help distinguish slow channel congenital myasthenic syndrome (SCCMS) from acquired myasthenia gravis (MG) We present a patient with fatigable weakness in whom afterdischarges were not initi...
Benign monomelic amyotrophy of the lower extremity: report of two cases and literature review [0.03%]
下肢良性单肢肌萎缩症两例报告及文献复习
M M Dimachkie,W Justiz,F J Vriesendorp
M M Dimachkie
Benign monomelic amyotrophy is an uncommon cause of progressive mildly disabling atrophy and weakness of a limb. It predominantly affects the distal upper limb of young men. We present two women with benign monomelic of amyotrophy of the lo...
J L Cosgrove
J L Cosgrove
To determine the indications for magnetic resonance imaging (MRI) in the evaluation of individuals with carpal tunnel syndrome (CTS). a critical review of the literature was undertaken. Among the studies reviewed, a lack of uniformity in MR...
K M Krajewski,M E Shy
K M Krajewski
Neuropathic ulcers [0.03%]
神经源性溃疡
M C Spires,A J Davis
M C Spires
J C Kincaid,H A Honark
J C Kincaid
Clinical Approach to Neuromuscular Weakness in the Critically III Patient [0.03%]
危重病人的神经肌肉无力的临床治疗方法
J V Campellone
J V Campellone
Neuromuscular disorders developing m critically ill patients often result in increased morbidity and prolonged intensive care hospitalization Detection and assessment of affected patients are frequently hindered by the severe nature of the ...