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Published in 2019 at "International Journal of Rheumatic Diseases"
DOI: 10.1111/1756-185x.13559
Abstract: Inflammatory idiopathic myositis (IIM) comprises a heterogeneous group of systemic muscular diseases that can occur together with other connective tissue diseases (CTD), named overlap myositis (OM). The question of whether OM is a distinct entity…
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Keywords:
myositis;
distinct entity;
entity beyond;
myositis distinct ... See more keywords
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Published in 2020 at "BMJ Case Reports"
DOI: 10.1136/bcr-2020-235173
Abstract: Rowell’s syndrome is a rare disorder characterised by an association of lupus erythematosus with erythema multiforme (EM)-like skin lesions. EM as the initial clinical presentation of systemic lupus erythematosus is also atypical and even rarer.…
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Keywords:
rare distinct;
entity rheumatology;
rowell syndrome;
syndrome rare ... See more keywords
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Published in 2020 at "Journal of Osseointegration"
DOI: 10.23805/jo.2020.12.01.03
Abstract: Aggressive periodontitis is a questionable disease with limited evidence supporting its incidence and mechanism. Till now, the genetic hypothesis is the most acceptable theory that supports its presence. According to literature, several unproven theories were…
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Keywords:
periodontitis distinct;
aggressive periodontitis;
distinct entity;
disease ... See more keywords
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Published in 2018 at "Journal of Pediatric Neurosciences"
DOI: 10.4103/jpn.jpn_53_18
Abstract: Neurocutaneous melanosis (NCM) is a rare congenital disorder. Most of the cases described in literature for this entity have involvement of the leptomeninges and other structures of brain such as brain stem, temporal lobes, and…
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Keywords:
neurocutaneous melanosis;
entity;
involvement leptomeninges;
bilateral temporal ... See more keywords