Recurrent critical illness myopathy in an asthmatic patient treated with corticosteroids [0.03%]
哮喘长期使用皮质类固醇患者的反复重症肌病
Y Lindenbaum,S P Nations,R J Barobn et al.
Y Lindenbaum et al.
We report a case of recurrent critical illness myopathy in an asthmatic patient who was treated for respiratory failure with high doses of intravenous corticosteroids alone without exposure to nondepolarizing neuronmscular-bloclong agents. ...
Z Odabasi,J A Brooks,D S Kim et al.
Z Odabasi et al.
We report the first study in which the repetitive nerve stimulation (RNS) test was performed in conjunction with the ice-pack test in three patients with myasthenia gravis. All three patients showed an unequivocal improvement in ptosis on t...
Rapidly progressive, acute polyradiculopathies and cranial neuropathies resulting from leptomeningeal nasal-type NK cell lymphoma [0.03%]
由脑膜型鼻自然杀伤细胞淋巴瘤所致的急性多发神经根病变和颅神经病变1例报告及文献复习
M Zaretsky,U Pulipaka,D Schiff et al.
M Zaretsky et al.
Lymphomas may cause polyradiculopathies by several pathogenic mechanisms. However, such a presentation of a nasal-type NK (natural killer) cell lymphoma is rare. We report a previously healthy man who developed acute, axon-loss radiculopath...
Lambert-eaton myasthenic syndrome: a harbinger to transitional cell carcinoma of the urinary bladder [0.03%]
莱姆病- Eaton 肌无力综合征：泌尿系统膀胱移行细胞癌的先兆
B Katirji
B Katirji
A 72-year-old man developed Lambert-Eaton myasthenic syndrome (LEMS) with typical electrodiagnostic findings and elevated serum antibodies to the P/Q-type voltage-gated calcium channels. Two years after diagnosis, he had transitional cell c...
Maternal Bilateral Radial Neuropathy During Childbirth in Hereditary Neuropathy With a Predisposition to Pressure Palsies (HNPP) [0.03%]
HNPP患者因分娩导致的双侧桡神经病变
F M Molloy,E M Raynor,S B Rutkove
F M Molloy
A 30-year-old woman developed severe bilateral radial neuropathies during vaginal delivery of twins, likely secondary to positioning and muscular effort. Subsequent evaluation led to the diagnosis of hereditary neuropathy with predispositio...
A Coin,G Enzi,M Bussolotto et al.
A Coin et al.
Objectives: : To assess the presence of mitochondria! dysfunction in 18 patients with multiple symmetric lipomatosis (MSL). Methods: : ...
Diagnostic value of nerve and muscle biopsy in suspected vasculitis cases [0.03%]
疑似血管炎患者的神经和肌肉活检的诊断价值
G C Claussen,T D Thomas,C Goyne et al.
G C Claussen et al.
Objectives: To evaluate the diagnostic value of nerve and muscle biopsy in suspected cases of vasculitis and their correlation with the clinical and electrophysiological data. ...
Paraneoplasic dermatomyositis sine dermatitis associated with a tumor of the renal excretion system [0.03%]
与泌尿系统肿瘤相关的无皮炎皮肤肌炎综合征病例报告
Tali-Anne Szwebel,Serge Perrot,Gérald Kierzek et al.
Tali-Anne Szwebel et al.
National trends in hospital outcomes among patients with Guillain-Barré syndrome requiring mechanical ventilation [0.03%]
Guillain-Barré综合征患者需要机械通气的住院结局的全国趋势
Nizar Souayah,Abu Nasar,M Fareed K Suri et al.
Nizar Souayah et al.
Several new treatments have been introduced for Guillain-Barré syndrome over the last decade. To assess the impact of these new strategies on outcomes and hospitalization charges among patients with Guillain-Barré syndrome requiring mecha...
Coincident trinucleotide repeat expansions in a patient with myotonic dystrophy type 1 and spinocerebellar ataxia [0.03%]
一名同时患有肌营养不良症1型和脊髓小脑共济失调患者的三核苷酸重复序列扩展突变分析报告
Stephen J Kolb,John T Kissel
Stephen J Kolb
This is a case report of a patient with confirmed myotonic dystrophy type 1 and spinocerebellar ataxia type 6. The coexistence of two trinucleotide repeat expansions in this family illustrates the importance of continued and vigilant diagno...