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A Compendious Account on the Significance of Gallstone Ileus in Amyotrophic Lateral Sclerosis

Vincent Marcucci

Gallstone Ileus (GI) is an uncommon pathology generally affecting elderly females with a history of untreated cholelithiasis. The development of GI is a sequel from a fistulous ..Voir plus»

Rapport de cas

Complete Bilateral Horizontal Gaze Palsy as Initial Manifestation of Multiple Sclerosis: A Case Report

Mohamed Salah Gamea1*, Ashraf AlAkkad2 and Reem Ibraheem3

Multiple sclerosis is a chronic inflammatory disease of central nervous system that commonly affects young adults. Although ocular movement disturbances are commonly encountered..Voir plus»

article de recherche

Lower Limb Motor Coordination of Stroke Survivors, Based Upon Their Levels of Motor Recovery and Ages

Kenia Kiefer Parreiras de Menezes, Aline Alvim Scianni, Iza Faria-Fortini, Patrick Roberto Avelino, Christina DCM Faria and Luci Fuscaldi Teixeira-Salmela

Objective: To describe the motor coordination (MC) of the paretic lower limb of stroke survivors based upon their levels of motor r..Voir plus»

Communication courtoise

A study of the effect of curcumin on plasma free radicals in cirrhotic rats using Bile Duct Ligation (BDL)

Davoud Javidmehr, Ali Moradi, Alireza Karimoalah, Hadi Zarezrdini, Hamidreza Shahmoradi, Khadije Arabbadkobe, Akbar Rezai-Chahoki, Tahere Barabadi, Fereshte Ahmadian

"Cirrhosis of the liver is an important cause of mortality in the world and results in about ten thousand deaths each year. Cirrhosis of the liver, due to its high prevalen..Voir plus»

Mini examen

Multiple the Role of Galectin-3 in Promoting Sufficient Myelination

Richard Green and Marshal Ray

Understanding the molecular basis of Central Nervous System (CNS) demyelination, remyelination, and hypomyelination is crucial for the development of future neuroregenerative th..Voir plus»

Rapport de cas

A Novel Mutation in the SCN4A Gene in a Japanese Family with Paramyotonia Congenita

Satoru Takahashi, Shiho Yamamoto, Ryosuke Tanaka, Akie Okayama, Akiko Araki, Hiroki Kajino and Hiroshi Azuma

Paramyotoniacongenita is an autosomal-dominant muscle disease caused by missense mutations in SCN4A, the
gene enconding the alpha subunit of skeletal muscle sodium channe..Voir plus»