Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Michael C. Isfort"'
Granulomatous Myositis Associated With Acetylcholine Receptor Antibodies Without Clinical Myasthenia
Publikováno v:
Journal of clinical neuromuscular disease. 23(1)
Myasthenia gravis associated with concurrent inflammatory myopathy is a rare but well-described syndrome, most often seen in patients with thymoma. We present a case of biopsy-proven granulomatous myositis associated with positive acetylcholine recep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9378812e91d1be2d148e41d26b6fe234
https://pubmed.ncbi.nlm.nih.gov/34431802
https://pubmed.ncbi.nlm.nih.gov/34431802
Publikováno v:
Life Sciences. 116:67-73
Pathologic and physiologic factors acting on the heart can produce consistent pressure changes, volume overload, or increased cardiac output. These changes may then lead to cardiac remodeling, ultimately resulting in cardiac hypertrophy. Exercise can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::918bd417c912c305b89ddeaae27a5cc7
https://doi.org/10.1016/j.lfs.2014.08.015
https://doi.org/10.1016/j.lfs.2014.08.015
Publikováno v:
Heart failure reviews. 19(1)
Diabetic cardiomyopathy (DCM) is defined as cardiac disease independent of vascular complications during diabetes. The number of new cases of DCM is rising at epidemic rates in proportion to newly diagnosed cases of diabetes mellitus (DM) throughout
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd8532c9de72b1918be4a5934550cb7b
https://pubmed.ncbi.nlm.nih.gov/23443849
https://pubmed.ncbi.nlm.nih.gov/23443849
Publikováno v:
The Application of Clinical Genetics. :235
Charcot-Marie-Tooth (CMT) disease is the most common hereditary polyneuropathy and is classically associated with an insidious onset of distal predominant motor and sensory loss, muscle wasting, and pes cavus. Other forms of hereditary neuropathy, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c6cce25f58f66be9845be684f73a287
https://doi.org/10.2147/tacg.s69969
https://doi.org/10.2147/tacg.s69969