Snehaldatta S Khade,Shrikant S Deshmukh,Pramod V Dhonde et al.
Snehaldatta S Khade et al.
Mirror movements [0.03%]
镜像运动
Nilesh A Nadkarni,Shrikant S Deshmukh
Nilesh A Nadkarni
Sudheeran Kannoth
Sudheeran Kannoth
Paraneoplastic neurological syndromes (PNS) are rare disorders associated with cancer, not caused by direct invasion, metastasis or consequences of treatment. They are usually autoimmune in nature. Often, PNS precedes the manifestations of ...
Chronic cerebrospinal venous insufficiency in Multiple Sclerosis: A note for caution [0.03%]
慢性脑脊髓静脉循环不全与多发性硬化症的关系——谨慎解读相关研究结果的通知书
Rohit Bhatia,Abhishek,Kameshwar Prasad
Rohit Bhatia
Change of guard [0.03%]
权力交接
Satish V Khadilkar
Satish V Khadilkar
Sumeet G Dua,Seema Kembhavi,Brijesh Arora
Sumeet G Dua
Coexistence of primary sclerosing cholangitis in a patient with myasthenia gravis [0.03%]
重症肌无力患者并发原发性硬化性胆管炎临床表现及发病机制的研究
P J Lorenzoni,R H Scola,C S K Kay et al.
P J Lorenzoni et al.
Myasthenia gravis (MG) is an immune-mediated disease that compromises the postsynaptic membrane of the neuromuscular junction. Primary sclerosing cholangitis (PSC) is considered an immune-mediated cholestatic liver disease. Both MG and PSC ...
Paroxysmal dystonic choreoathetosis with symptomatic seizures secondary to hypoglycemia caused by insulinoma [0.03%]
由胰岛细胞瘤引起低血糖继发的症状性癫痫发作伴有肌张力障碍手足徐动症
Meena Gupta,Amit Batra,Makarand Hirve et al.
Meena Gupta et al.
Neurological syndromes are not an uncommon presentation with insulinomas. Recurrent hypoglycemia associated with it can present with a variety of neurological symptoms that may include disturbances of consciousness, seizures, stroke-like pr...
Ajay Gulati,Paramjeet Singh,Subramaniyan Ramanathan et al.
Ajay Gulati et al.
Triad of leukoencephalopathy, cerebral calcifications and cysts (LCC) is a recently reported rare disease named 'Labrune syndrome' after the first case was reported in 1996 by Labrune et al. Herein, we report a case of a 36-year-old man wit...
Ilham Ratbi,Siham Chafai Elalaoui,Adela Escudero et al.
Ilham Ratbi et al.
Myotonia congenita is a genetic muscle disorder characterized by clinical and electrical myotonia, muscle hypertrophy, and stiffness. It is inherited as either autosomal-dominant or -recessive, known as Thomsen and Becker diseases, respecti...