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Embolic Agents: Sclerotherapy.
Patterns of ovarian and luteal activity in captive and wild Canada lynx (Lynx canadensis).
Synthesizing pseudo-T2w images to recapture missing data in neonatal neuroimaging with applications in rs-fMRI.
Survival after cardiopulmonary resuscitation in babies of very low birth weight. Is CPR futile therapy?
Percutaneous subxiphoid access to the epicardium using a miniature crawling robotic device.
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Wollmann, Robert
One or more keywords matched the following items that are connected to
Wollmann, Robert
Item Type
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Concept
Myasthenia Gravis
Academic Article
The beta 2-adrenergic agonist terbutaline suppresses acute passive transfer experimental autoimmune myasthenia gravis (EAMG).
Academic Article
The human-severe combined immunodeficiency myasthenic mouse model: a new approach for the study of myasthenia gravis.
Academic Article
Slow-channel transgenic mice: a model of postsynaptic organellar degeneration at the neuromuscular junction.
Academic Article
Genetic manipulation of AChR responses suggests multiple causes of weakness in slow-channel syndrome.
Academic Article
Striational autoantibodies in myasthenia gravis patients recognize I-band titin epitopes.
Academic Article
Inflammation at the neuromuscular junction in myasthenia gravis.
Academic Article
Refractoriness to a second episode of experimental myasthenia gravis. Correlation with AChR concentration and morphologic appearance of the postsynaptic membrane.
Academic Article
Induction of the morphologic changes of both acute and chronic experimental myasthenia by monoclonal antibody directed against acetylcholine receptor.
Academic Article
The hu-SCID myasthenic mouse. A new tool for the investigation of seronegative myasthenia gravis.
Academic Article
Patients with myasthenia gravis and thymoma have in their sera IgG autoantibodies against titin.
Academic Article
Acute severe animal model of anti-muscle-specific kinase myasthenia: combined postsynaptic and presynaptic changes.
Academic Article
Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia.
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Myasthenia Gravis