Relevant bibliographies by topics / Myasthena gravis

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Myasthena gravis'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Myasthena gravis"

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SANDERS, DONALD B., and ERIK STALBERG. "The Overlap Between Myasthena Gravis and Lambert-Eaton Myasthenic Syndrome." Annals of the New York Academy of Sciences 505, no. 1 Myasthenia Gr (1987): 864–65. http://dx.doi.org/10.1111/j.1749-6632.1987.tb51394.x.

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Bufler, J. "Diagnostik und Therapie der Myasthenia gravis und anderer myasthener Syndrome." Nervenheilkunde 27, no. 07 (2008): 664–72. http://dx.doi.org/10.1055/s-0038-1627127.

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ZusammenfassungBelastungsabhängige Paresen sind das Kardinalsymptom neuromuskulärer synaptischer Übertragungsstörungen. Diese Erkrankungen sind klinisch durch belastungsabhängige Paresen und abnorme Ermüdbarkeit der quergestreiften Muskulatur einschließlich der okulären, bulbären und respiratorischen Muskeln charakterisiert. Die Myasthenia gravis ist die häufigste Erkrankung aus diesem Formenkreis und stellt den Schwerpunkt der vorliegenden Übersicht dar. Im letzten Drittel des 19. Jahrhunderts wurden zahlreiche Fallbeschreibungen von Patienten mit belastungsabhängigen Paresen, Bulbärsymptomat
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Kruglyakov, N. M., D. G. Levitova, G. I. Bagzhanov, et al. "Application of the Technique of Extracorporeal Membrane Oxygenation in a Patient With Respiratory Distress Syndrome Associated With Myasthenia Gravis." Russian Sklifosovsky Journal "Emergency Medical Care" 10, no. 2 (2021): 393–400. http://dx.doi.org/10.23934/2223-9022-2021-10-2-393-400.

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Myasthenia gravis is an autoimmune neuromuscular disease characterized by pathologically rapid fatigue of striated muscles [1]. The main symptom of myasthenia gravis is the presence of pathological muscle weakness with involvement of the ocular, bulbar and skeletal muscles in the pathological process. The provoking factors for the development of myasthenia gravis can be infectious diseases, surgery, drugs [2, 3]. The main danger is represented by myasthenic and cholinergic crises, which are characterized by a severe course and high mortality; therefore, the problems of treating myasthenia grav
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Nicolle, Michael W. "Pseudo-Myasthenia Gravis and Thymic Hyperplasia in Graves’ Disease." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 26, no. 3 (1999): 201–3. http://dx.doi.org/10.1017/s0317167100000251.

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Background:Diagnostic confusion between thyroid disease and myasthenia gravis (MG) can arise because the two may have similar clinical features, and also because of the more frequent coexistence of these autoimmune disorders in the same individual. In MG, autoantibodies directed against the acetylcholine receptor result in muscle weakness. Thymic pathology is well recognized in MG, with thymic hyperplasia frequent in early onset MG and thymoma more common in later onset MG. In Graves’ disease, autoantibodies against thyroid antigens result in hyperthyroidism. A seldom-recognized feature of Gra
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Hoffmann, Sarah, and Andreas Meisel. "Therapierefraktäre Verläufe und Eskalationsstrategien in der Behandlung der Myasthenia gravis." Aktuelle Neurologie 45, no. 04 (2018): 294–97. http://dx.doi.org/10.1055/s-0043-125360.

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ZusammenfassungTherapierefraktäre Verläufe der Myasthenia gravis (MG) mit Versagen auf oder Kontraindikationen für die (erweiterte) Standardtherapie sind mit 10 – 15 % aller Myasthenie-Patienten selten. Die aktuellen internationalen Konsens-Leitlinien für die Behandlung der MG empfehlen die Zuweisung von therapierefraktären Patienten an ein Zentrum mit Erfahrung in der Behandlung der MG sowie den Einsatz von intravenösen Immunglobulin- oder Plasmapherese-Therapien. Bei Fehlen von Kontraindikationen ist zur Kontrolle der myasthenen Symptome jedoch zusätzlich der Einsatz von Langzeit-Immunsuppre
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Mallikarjuna, Sathish Kumar, S. Sakthi Velayutham, P. R. Sowmini, Malcolm K. Jeyaraj, and S. Arunan. "See-Saw Relationship and its Reversal after Immunotherapy in a Case of Graves’ Disease with Coexisting Myasthenia Gravis." Journal of Neurosciences in Rural Practice 10, no. 01 (2019): 136–38. http://dx.doi.org/10.4103/jnrp.jnrp_150_18.

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ABSTRACTThe unique association of myasthenia gravis (MG) with Graves' disease in clinical practice emphasizes that one autoimmune disease can coexist with another or many. The relationship between these two entities has remained controversial till date. Some authors have reported a see-saw relationship between these two entities, MG waning with hyperthyroidism and waxing with treatment of hyperthyroidism. Treatment of both these disorders concurrently may be challenging at times as treatment for one entity may worsen the other. The use of beta-blockers and steroids for Graves' disease may wors
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Job, Anand, R. Raman, and C. Gnanamuthu. "Laryngeal stridor in myasthenia gravis." Journal of Laryngology & Otology 106, no. 7 (1992): 633–34. http://dx.doi.org/10.1017/s0022215100120390.

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AbstractTwo patients with laryngeal stridor secondary to myasthenia gravis are reported. The cause of bilateral abductor weakness in myasthenia is discussed; anticipation of the stridor in myasthenic patients is highlighted.
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Su Fuia, Thung, Raja Ahmad Reza Raja Lope Ahmad, and Rose Izura Abdul Hamid. "P-NJ002. Myasthena gravis, a great ‘mimicker’ as an initial autoimmune presentation of diffused large B cell lymphoma: a case report." Clinical Neurophysiology 132, no. 8 (2021): e103-e104. http://dx.doi.org/10.1016/j.clinph.2021.02.245.

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Saraiva, Paulo A. P., José Lamartine de Assis, and Paulo E. Marchiori. "Evaluation of the respiratory function in myasthenia gravis: an important tool for clinical feature and diagnosis of the disease." Arquivos de Neuro-Psiquiatria 54, no. 4 (1996): 601–7. http://dx.doi.org/10.1590/s0004-282x1996000400009.

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Myasthenic gravis may affect both inspiratory and expiratory muscles. Respiratory involvement occurred in almost all patients with myasthenia gravis in all clinical forms of the disease: 332 lung function tests done in 324 myasthenic patients without respiratory symptoms (age 34.6 ± 18.3 years) were examined. Lung volumes analysis showed that all the patients of both sexes with generalized or ocular myasthenia gravis showed "myasthenic pattern". Male patients with "ocular" form only presented the "myasthenic pattern" with lung impairment and had, from the lung function point of view, a more be
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Marouf, W., and J. P. Sieb. "Myasthenia gravis und myasthene Syndrome." Zeitschrift für Rheumatologie 68, no. 6 (2009): 465–70. http://dx.doi.org/10.1007/s00393-009-0456-0.

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Dissertations / Theses on the topic "Myasthena gravis"

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Barrett-Jolley, Richard A. "Effects of plasma from seronegative myasthenics and controls on receptor and voltage gated membrane currents of TE671 cells." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334228.

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Simpson, John Alexander. "Myasthenia gravis." Thesis, University of Edinburgh, 1991. http://hdl.handle.net/1842/27395.

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The thesis is 72 publications describing the author's hypothesis of an autoimmune basis for myasthenia gravis (MG) and its validation. At the time of the first 24 papers many considered that MG was a syndrome rather than a disease entity, due to a biochemical disorder of the neuromuscular junction. Favoured models were a circulating 'curare-like' substance released from the thymus gland, or a pre-junctional abnormality, possibly causing release of small quanta of acetylcholine at the motor nerve terminals. Endplate receptor substance was speculative. The immunological role of the thymus was un
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Carr, A. S. "An epidemiological study of myasthenia gravis and congenital myasthenic syndromes in Northern Ireland." Thesis, Queen's University Belfast, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546021.

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da, Silva Leite Maria Isabel. "Myasthenia Gravis: Investigations into Seronegative Myasthenia." Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.490100.

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Myasdienia gravis (MG) is an antibody-mediated autoimmune disease causing muscle weakness and fatigue. Over 80% of patients with generalised MG have IgG autoantibodies (mostly IgUlj to the native muscle acetylcholine receptor (AChR) at the neuromuscular junction (NM]). AChR-antibody-positive MG (AChR-MG) patients often benefit from thymectomy. Their thymus usually has epithelial hyperplasia and the thymus is thought to be the site of autoimmunisation against AChR. Of the remaining 15-20% of patients with generalised MG, a variable proportion (0-50%) have autoantibodies to muscle-specific kinas
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Verschuuren, Johannes Justus Gerard Maria. "Experimental autoimmune myasthenia gravis." Maastricht : Maastricht : Datawyse ; University Library, Maastricht University [Host], 1989. http://arno.unimaas.nl/show.cgi?fid=5471.

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Schaffert, Hanne. "Immunpathogenese der Myasthenia gravis." Doctoral thesis, Humboldt-Universität zu Berlin, Lebenswissenschaftliche Fakultät, 2015. http://dx.doi.org/10.18452/17213.

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Die Myasthenia Gravis (MG) ist ein Prototyp einer Antikörper-vermittelte Autoimmunerkrankung. Die Autoantikörper richten sich hauptsächlich gegen den Acetylcholinrezeptor (AChR). Welche Bedeutung TH17-Zellen für die Pathogenese der MG haben, konnte bisher noch nie direkt gezeigt werden. Mithilfe des Tiermodells Experimentelle Autoimmune Myasthenia Gravis (EAMG) sollte die Rolle der TH17-Zellen im Rahmen dieser Arbeit analysiert werden. Eine signifikante Anzahl tAChR-spezifischer CD4+ T-Zellen, die IL17 exprimieren, konnte nach der Immunisierung mit torpedo AChR in CFA in Wildtyp-Mäusen (WT) be
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Kaufman, Robin L. "Immunoregulation in myasthenia gravis." Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/30683.

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Myasthenia Gravis (MG) is an autoimmune disorder of neuromuscular transmission. Clinically, the disease is manifested by abnormal muscle fatigue with recovery on resting. Circulating nicotinic acetylcholine receptor antibodies (nAchR Ab) are highly characteristic of myasthenia gravis. These antibodies have been shown to be directly pathogenic at the muscle endplate and are responsible for impaired neuromuscular transmission through several mechanisms. While it is clear that the immune system does not function normally in MG, the mechanisms by which the response to nAchR is initiated and perpe
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McConville, John Paul. "Autoantibodies in seronegative myasthenia gravis." Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400295.

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Shi, Fu-Dong. "Immunopathogenesis and nasal tolerance in experimental autoimmune myasthenia gravis /." Stockholm, 1998. http://diss.kib.ki.se/search/diss.se.cfm?19980525shi.

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VILQUIN, JEAN-THOMAS. "Contribution a la comprehension, au traitement et au diagnostic de la myasthenia gravis." Strasbourg 1, 1992. http://www.theses.fr/1992STR15067.

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Books on the topic "Myasthena gravis"

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Baets, M. H. De, 1950-, Oosterhuis, Henricus Josephus Gerardus Hubertus., and Toyka K. V. 1945-, eds. Myasthenia gravis. Karger, 1988.

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Christadoss, Premkumar, ed. Myasthenia Gravis. Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4060-7.

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Giovanni, Giacalone. Contributo della pranoterapia nella myasthenia gravis =: Pranotherapy help in the myasthenia gravis. Edizioni G. & G., 1986.

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service), SpringerLink (Online, ed. Myasthenia Gravis and Related Disorders. Humana Press, 2009.

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Kaminski, Henry J. Myasthenia Gravis and Related Disorders. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-156-7.

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Kaminski, Henry J., ed. Myasthenia Gravis and Related Disorders. Humana Press, 2003. http://dx.doi.org/10.1007/978-1-59259-341-5.

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Kaminski, Henry J., and Linda L. Kusner, eds. Myasthenia Gravis and Related Disorders. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-73585-6.

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Kaminski, Henry J. Myasthenia Gravis and Related Disorders. Humana Press, 2002. http://dx.doi.org/10.1385/1592593410.

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Giacalone, Giovanni. Pranotherapy help in the myasthenia gravis. [s.n.], 1986.

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Parker, James N., and Philip M. Parker. The official patient's sourcebook on myasthenia gravis. Icon Health Publications, 2002.

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Book chapters on the topic "Myasthena gravis"

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Swash, Michael, and Martin S. Schwartz. "Myasthenia Gravis and Other Myasthenic Syndromes." In Neuromuscular Diseases. Springer London, 1997. http://dx.doi.org/10.1007/978-1-4471-3834-1_12.

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Swash, Michael, and Martin Schwartz. "Myasthenia Gravis and Other Myasthenic Syndromes." In Neuromuscular Diseases. Springer London, 1988. http://dx.doi.org/10.1007/978-1-4471-3526-5_12.

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Gorshtein, Alexander, and Yair Levy. "Myasthenia Gravis." In Diagnostic Criteria in Autoimmune Diseases. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-285-8_74.

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Austin, Jane, and Pierre A. Leon. "Myasthenia Gravis." In Encyclopedia of Clinical Neuropsychology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_565.

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Jordan, B., and S. Zierz. "Myasthenia gravis." In Klinische Neurologie. Springer Berlin Heidelberg, 2020. http://dx.doi.org/10.1007/978-3-662-44768-0_41-2.

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Jordan, B., and S. Zierz. "Myasthenia gravis." In Klinische Neurologie. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-44768-0_41-1.

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Tindall, Richard S. A. "Myasthenia Gravis." In Foundations of Neurology. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1495-0_19.

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Evoli, Amelia, and Raffaele Iorio. "Myasthenia Gravis." In Acquired Neuromuscular Disorders. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29514-5_9.

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Voit, T. "Myasthenia gravis." In Pädiatrie. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-76460-1_216.

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Thakore, Nimish. "Myasthenia Gravis." In Encyclopedia of Women’s Health. Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48113-0_289.

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Conference papers on the topic "Myasthena gravis"

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Wu, D., D. Condit, and J. C. Nascimento. "Pembrolizumab Induced Myasthenia Gravis." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a2408.

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Malladi, S., A. Aburahma, L. Rashdan, and K. Ranabhat. "The Many Faces of Myasthenia Gravis." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a2296.

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Liang, T., M. I. Boulos, B. J. Murray, S. Krishnan, H. Katzberg, and K. Umapathy. "Detection of myasthenia gravis using electrooculography signals." In 2016 38th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2016. http://dx.doi.org/10.1109/embc.2016.7590845.

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Ceylan, Kenan Can, Seyda Ors Kaya, Ozgur Ozturk, Yasar Zorlu, and Muhtesem Gedizlioglu. "Minimally Invasive Thymectomy in Non-Thymomatous Myasthenia Gravis Cases." In ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.pa2056.

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Schweitzer, M. D., P. A. Barletta, and M. Mirsaeidi. "Late-Onset Sarcoidosis in a Patient with Myasthenia Gravis." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a1543.

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Totzeck, A., S. Bolz, K. Kizina, B. Stolte, C. Kleinschnitz, and T. Hagenacker. "Neue Horizonte – Das Darmmikrobiom als Pathogenesefaktor bei der Myasthenia gravis." In 24. Kongress des Medizinisch-Wissenschaftlichen Beirates der Deutschen Gesellschaft für Muskelkranke (DGM) e.V. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1685109.

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Kankanala, V. L., and N. Kotecha. "Myasthenia Gravis: A Rare Immune Related Adverse Event of Pembrolizumab." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a6542.

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Correa, V., J. R. Vintch, and M. Adler. "Abrupt Respiratory Failure as Initial Presentation of Myasthenia Gravis Crisis." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a1771.

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Ick, H., and J. Kluge. "Thymektomie bei Myasthenia gravis und/oder Thymom – Indikation und operatives Vorgehen." In 13. Herbsttagung der Mitteldeutschen Gesellschaft für Pneumologie und Thoraxchirurgie. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0037-1613658.

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Azri, Muhammad, Stephanie Young, Hazel Lin, Clement Tan, and Zhi Yang. "Diagnosis of Ocular Myasthenia Gravis by means of tracking eye parameters." In 2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2014. http://dx.doi.org/10.1109/embc.2014.6943876.

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Reports on the topic "Myasthena gravis"

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Asenova, Asya, and Veneta Bojinova. Juvenile Myasthenia Gravis - Clinical Course and Serologic Tests. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2020. http://dx.doi.org/10.7546/crabs.2020.12.17.

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Xie, Rongfang, Liting Liu, Ruiqi Wang, and Chunhua Huang. Traditional Chinese medicine for Myasthenia gravis: study protocol for a network meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2020. http://dx.doi.org/10.37766/inplasy2020.6.0049.

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Peng, Yuxuan, Lu Li, Yuting Pan, et al. External treatment of Traditional Chinese Medicine for myasthenia gravis: a protocol for systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2021. http://dx.doi.org/10.37766/inplasy2021.1.0083.

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Li, Lu, Jiachun Lu, BiBo Lu, et al. Tonifying Spleen and Replenishing Kidney method of Traditional Chinese Medicine for myasthenia gravis: a protocol for systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2021. http://dx.doi.org/10.37766/inplasy2021.1.0097.

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Surgery to remove the thymus gland improves weakness for people with myasthenia gravis. National Institute for Health Research, 2016. http://dx.doi.org/10.3310/signal-000310.

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