Acta Myologica Online [0.03%]
在线肌学杂志
Vincenzo Nigro
Vincenzo Nigro
Minutes of the European POmpe Consortium (EPOC) Meeting March 27 to 28, 2015, Munich, Germany [0.03%]
2015年3月27日至28日在德国慕尼黑召开的欧洲庞培病联盟(EPOC)会议纪要
Benedikt Schoser,Pascal Laforêt,Michelle E Kruijshaar et al.
Benedikt Schoser et al.
Rhabdomyolysis in hyponatremia and paraneoplastic syndrome of inappropriate antidiuresis [0.03%]
低钠血症和异位抗利尿激素综合征伴横纹肌溶解症
Elisabetta D&#x;Adda,Rosina Paletta,Fabio Brusaferri et al.
Elisabetta D&#x;Adda et al.
We report a 26-year-old woman admitted to our hospital for generalized tonic seizure. Laboratory investigations revealed severe hyponatremia possibly triggered by vomiting and diarrhea. 24 hours after correction of hyponatremia she develope...
Muscle histology changes after short term vibration training in healthy controls [0.03%]
健康受试者短期振动训练后的肌肉组织学变化
Benedikt Schoser
Benedikt Schoser
In search for additional counter measures of muscle atrophy vibration exercise training may have substantial effort for patients with neuromuscular disorders. To cover safety aspects and obtain muscle morphology data, a pilot study was perf...
Marina Peric,Stojan Peric,Nada Rapajic et al.
Marina Peric et al.
To analyze the frequency and intensity of pain and its association with different characteristics of patients with myotonic dystrophy type 1 (DM1) and type 2 (DM2), 52 adult genetically confirmed DM1 and 44 DM2 patients completed the Brief ...
A multi-parametric protocol to study exercise intolerance in McArdle's disease [0.03%]
用于研究麦卡德尔病运动不耐受的多参數协议
Giulia Ricci,Federica Bertolucci,Annalisa Logerfo et al.
Giulia Ricci et al.
McArdle's disease is the most common metabolic myopathy of muscle carbohydrate metabolism, due to deficiency of myophosphorylase and alteration of glycogen breakdown in muscle. The clinical manifestations usually begin in young adulthood, w...
Roberta Petillo,Paola D&#x;Ambrosio,Annalaura Torella et al.
Roberta Petillo et al.
Mutations in the lamin A/C gene (LMNA) have been associated with several phenotypes ranging from systemic to prevalent of muscle, heart, skin, nerve etc. More recently they have been associated with dilated cardiomyopathy (DCM) and severe f...
Imaging alterations in skeletal muscle channelopathies: a study in 15 patients [0.03%]
15例肌肉通道病的肌内影像学改变研究
Lorenzo Maggi,Raffaella Brugnoni,Eleonora Canioni et al.
Lorenzo Maggi et al.
Skeletal muscle channelopathies (SMC), including non dystrophic myotonias (NDM) and periodic paralyses (PP), are characterized by considerable clinical overlap and clinical features not always allow addressing molecular diagnosis. Muscle im...
Jordi Díaz-Manera,Jaume Llauger,Eduard Gallardo et al.
Jordi Díaz-Manera et al.
Muscle MRI has become a very useful tool in the diagnosis and follow-up of patients with muscle dystrophies. Muscle MRI provides us about many aspects of the structure and function of skeletal muscles, such as the presence of oedema or fatt...
Luisa Politano,Giovanni Nigro
Luisa Politano