Patient registries: useful tools for clinical research in myasthenia gravis-Reference-Cited by-同舟云学术

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Patient registries: useful tools for clinical research in myasthenia gravis

Published:2012-12 Issue:1 Volume:1274 Page:107-113
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:

Author:

Baggi Fulvio,Mantegazza Renato,Antozzi Carlo,Sanders Donald

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.2012.06771.x/fullpdf

Reference8 articles.

1. Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America;Jaretzki;Neurology,2000

2. A simple manual muscle test for myasthenia gravis: validation and comparison with the QMG score;Sanders;Ann. N.Y. Acad. Sci.,2003

3. The MG composite: a valid and reliable outcome measure for myasthenia gravis;Burns;Neurology,2010

4. Studies in myasthenia gravis: review of a twenty-year experience in over 1200 patients;Osserman;Mt. Sinai J. Med.,1971

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1. Therapeutic challenges and unmet needs in the management of myasthenia gravis: an Italian expert opinion;Neurological Sciences;2024-07-05

2. Clinical Profile and Quality of Life in Myasthenia Gravis Using MGQOL15 R(Hindi): An Indian Perspective;Annals of Indian Academy of Neurology;2023

3. The applicability of the myasthenia gravis patient registry data to disease burden and medication changes in clinical practice;Muscle & Nerve;2022-08-08

4. The D uke myasthenia gravis clinic registry: I . D escription and demographics;Muscle & Nerve;2020-12-05

5. Exploring outcomes and characteristics of myasthenia gravis: Rationale, aims and design of registry – The EXPLORE-MG registry;Journal of the Neurological Sciences;2020-07

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