Amyopathic dermatomyositis prognosis
[DOCX File]livrepository.liverpool.ac.uk
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dermatomyositis, and. polymyositis ... Treatment and Prognosis[edit] Unfortunately, treatment for the anti-synthetase syndrome is limited, and usually involves
[DOCX File]LOP_tianno
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Indexing terms used for the electronic search (("Case-Control Studies"[Mesh] OR "Cohort Studies"[Mesh] OR "Cross-Sectional Studies"[Mesh]) AND ("the British Journal of Dermatology" [journal] OR ...
[DOC File]Rheumatology 2002
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The overall prognosis was better than reported in adult series. Conclusion This is the largest multicenter study defining the demographic data for childhood vasculitides. The distribution of childhood vasculitides was different in our population where KD is much less frequent, whereas HSP constitutes an overwhelming majority.
Amyopathic dermatomyositis: retrospective review of 37 cases.
15. Gerami P, Schope JM, McDonald L, Walling HW, Sontheimer RD.A systematic review of adult-onset clinically amyopathic dermatomyositis (dermatomyositis siné myositis): a missing link within the spectrum of the idiopathic inflammatory myopathies. J Am …
[DOCX File]Pitfalls in the Diagnosis of Myositis
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They also varied in paradigmatic physiologic and pathologic situations associated with variations of capillary density, including amyopathic dermatomyositis, a unique condition in which muscle capillary loss occurs without myofiber damage, and in athletes, in whom capillaries increase in number.
[DOC File]The journal of investigate dermatology: Septembre 2010
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The prognosis varies with the type of neurologic process. Those with dural venous thrombosis or other non-parenchymal process are less likely to have recurrent disease, disability, or premature death. ... Polymyositis, Dermatomyositis, and Inclusion Body Myositis ... aMyopathic muscle weakness, affecting proximal muscles more than distal ones ...
MYOBASE
Autoantibodies in juvenile-onset myositis: their diagnostic value and associated clinical phenotype in a large UK cohort.. Authors. Sarah L Tansley a,b, Stefania Simou c, Gavin Shaddickd, Zoe E Betteridgeb, Beverley Almeidac,e, Harsha Gunawardenaf, Wendy Thomsong, Michael W Beresfordh,I,j, Angela Midgleyh,j, Francesco Muntonik, Lucy R Wedderburn *c,e,l & Neil J McHugh *a,b on behalf of the JDRG
[DOC File]Defining cancer-risk, and assessing diagnostic usefulness ...
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6. Bendewald MJ, Wetter DA, Li X, Davis MD. Incidence of dermatomyositis and clinically amyopathic dermatomyositis: a population-based study in Olmsted County, Minnesota. Arch Dermatol. 2010;146:26-30. 7. Lundberg IE, Forbess CJ. Mortality in idiopathic inflammatory myopathies. Clin Exp Rheumatol. 2008 Sep-Oct;26(5 Suppl 51):S109-14. 8.
Ines Maria Grazia PIRODDI,Gianluca FERRAIOLI*,Cornelius ...
Alveolar hemorrhage in cryoglobulinemia--an indicator of poor prognosis. Clin Exp Rheumatol. 23:616-20,2005. Amital H, Heilweil M, Ulmansky R, Szafer F, Bar-Tana R, Morel L, Foster MH, Mostoslavsky G, Eilat D, Pizov G, Naparstek Y. ... Amyopathic dermatomyositis- …
[DOC File]University of Pittsburgh
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The idiopathic inflammatory myopathies are a group of heterogenous autoimmune connective tissue diseases. Despite increase in the understanding of these conditions, securing a timely diagnosis and accurate subtype classification remains difficult in some cases.
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