collection
https://read.qxmd.com/read/24947881/antititin-antibody-in-early-and-late-onset-myasthenia-gravis
#21
JOURNAL ARTICLE
P Szczudlik, B Szyluk, M Lipowska, B Ryniewicz, J Kubiszewska, M Dutkiewicz, N E Gilhus, A Kostera-Pruszczyk
OBJECTIVES: Myasthenia gravis (MG) is an autoimmune disease caused by antibodies against neuromuscular junction proteins, 85% of patients have antibodies against acetylcholine receptor (AChR-MG). Antititin antibodies are present in a subset of patients with MG. We aimed to determine the value of antititin antibodies as severity markers and thymoma predictors in early- and late-onset MG. MATERIALS & METHODS: Two-hundred and ninety-five consecutive MG patients (188 F and 107 M) aged 12-89 years (mean 50y) were included...
October 2014: Acta Neurologica Scandinavica
https://read.qxmd.com/read/24117026/myasthenia-gravis-an-update-for-the-clinician
#22
REVIEW
J P Sieb
This paper provides a thorough overview of the current advances in diagnosis and therapy of myasthenia gravis (MG). Nowadays the term 'myasthenia gravis' includes heterogeneous autoimmune diseases, with a postsynaptic defect of neuromuscular transmission as the common feature. Myasthenia gravis should be classified according to the antibody specificity [acetylcholine, muscle-specific receptor tyrosine kinase (MuSK), low-density lipoprotein receptor-related protein 4 (LRP4), seronegative], thymus histology (thymitis, thymoma, atrophy), age at onset (in children; aged less than or more than 50 years) and type of course (ocular or generalized)...
March 2014: Clinical and Experimental Immunology
https://read.qxmd.com/read/21562253/comparison-of-ivig-and-plex-in-patients-with-myasthenia-gravis
#23
RANDOMIZED CONTROLLED TRIAL
D Barth, M Nabavi Nouri, E Ng, P Nwe, V Bril
OBJECTIVE: Both IV immunoglobulin (IVIg) and plasma exchange (PLEX) are immunomodulatory treatments used to treat patients with myasthenia gravis (MG), but the choice of which treatment to administer to patients is limited due to lack of evidence from adequately powered, masked, randomized, standardized trials. METHODS: We randomized 84 patients with moderate to severe MG defined as a Quantitative Myasthenia Gravis Score for disease severity (QMGS) of >10.5 and worsening weakness to IVIg (Gamunex®, Talecris Biotherapeutics) 1 g/kg/day for 2 consecutive days or PLEX (Caridian Spectra) 1...
June 7, 2011: Neurology
https://read.qxmd.com/read/11515619/the-outcome-in-myasthenia-gravis-patients-an-eight-year-follow-up-after-finishing-immunoabsorption-therapy
#24
JOURNAL ARTICLE
J M Schneidewind, U K Zettl, R E Winkler, W Ramlow, M Tiess, A Michelsen, G Hebestreit, H Prophet, W Pätow, R Benecke
Eight years ago four patients suffering from myasthenia gravis (MG) type C and E according to Compston with failed drug therapy were treated three times (one patient 11 times) by protein A immunoabsorption (Immunosorba, Excorim, Fresenius Hemocare GmbH, StWendel, Germany). No further immunoabsorption treatments have been carried out. In addition, three patients were given a thymectomy. The present status of the patients was checked six and eight years thereafter. We could see a beneficial effect in all MG patients...
February 2001: Transfusion and Apheresis Science
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