Results 81 to 90 of about 27,299 (305)

Circulating Fetuin‐A concentrations in rheumatic diseases: a systematic review and meta‐analysis

open access: yesEuropean Journal of Clinical Investigation, Volume 55, Issue 5, May 2025.
In this systematic review with meta‐analysis, we identified 19 eligible studies to determine whether there is any change in Fetuin‐A (FtA) concentrations in patients with rheumatic diseases. We observed a significant decrease in FtA concentrations in RD patients (standardized mean difference, SMD = −.91; 95% CI −1.43 to −.39, p = .001).
Biagio Di Lorenzo   +6 more
wiley   +1 more source

Spontaneous kidney rupture in a patient with polyarteritis nodosa

open access: yesJournal of Research in Medical Sciences, 2006
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects the medium- and small-sized arteries. It involves the renal arterioles in approximately 80% of cases, but spontaneous retroperitoneal hemorrhage is a rare complication of ...
Ahmad Mohammadi   +2 more
doaj  

Spontaneous Retroperitoneal Hematoma: A Rare Presentation of Polyarteritis Nodosa

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2019
Spontaneous retroperitoneal hematoma is a rare clinical entity that is most commonly caused by renal tumors and vascular disease. In this article, we present a case of spontaneous retroperitoneal hemorrhage caused by polyarteritis nodosa in a patient who
Asad Ullah MD   +4 more
doaj   +1 more source

Cutaneous polyarteritis nodosa: A case report with a brief review of literature

open access: yesMedical Journal of Dr. D.Y. Patil University, 2013
Polyarteritis nodosa (PAN) is a rare vasculitis with multisystem involvement. The definition, diagnostic criteria and validity of cutaneous polyarteritis nodosa (c-PAN) as a variant of classic PAN limited to skin have continued to remain disputed.
Yugal K Sharma   +3 more
doaj   +1 more source

Cutaneous Polyarteritis Nodosa Presented with Digital Gangrene: A Case Report [PDF]

open access: yes, 2006
Cutaneous polyarteritis nodosa (CPAN) is an uncommon form of vasculitis involving small and medium sized arteries of unknown etiology. The disease can be differentiated from polyarteritis nodosa by its limitation to the skin and lack of progression to ...
Albornoz   +21 more
core   +2 more sources

The Successful Treatment of Refractory Polyarteritis Nodosa Using Infliximab

open access: yesInternal medicine, 2017
Polyarteritis nodosa (PAN), characterized by arteritis of medium-sized blood vessels, is usually treated with a combination of glucocorticoids and immunosuppressants; however, some cases are refractory to these treatments.
S. Matsuo   +9 more
semanticscholar   +1 more source

New insights into the population genetics of partially clonal organisms: when seagrass data meet theoretical expectations [PDF]

open access: yesarXiv, 2019
Seagrass meadows are among the most important coastal ecosystems, in terms of both spatial extent and ecosystem services, but they are also declining worldwide. Understanding the drivers of seagrass meadow dynamics is essential for designing sound management, conservation, and restoration strategies.
arxiv  

Polyarteritis nodosa with uterine involvement [PDF]

open access: yesActa Radiologica Open, 2012
Polyarteritis nodosa (PAN) is characterized by multisystem necrotizing vasculitis, primarily affecting small-to-medium-sized muscular arteries, and it is typically found in middle-aged men.
Chihiro Hirai   +6 more
doaj   +1 more source

Pseudovasculitis and corticosteroid therapy [PDF]

open access: yes, 2018
Pseudovasculitis, vasculitis-like syndromes, vasculitis look-alikes, or mimics of vasculitis represent a heterogeneous collection of disorders that are capable of simulating vasculitis.
Egger, Jean-François   +4 more
core  

Sendotypes predict worsening renal function in chronic kidney disease patients

open access: yesClinical and Translational Medicine, Volume 15, Issue 4, April 2025.
Graphical abstract of the CKD sendotype discovery pipeline demonstrating the use of multiple omic datasets from patient plasma, patient biopsies and kidney organoid models for both clustering and validation. Abstract Background Senescence associated secretory phenotype (SASP) contributes to age‐related pathology, however the role of SASP in Chronic ...
Thomas McLarnon   +11 more
wiley   +1 more source

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