Results 121 to 130 of about 785 (150)
Some of the next articles are maybe not open access.
[Eosinophilic granulomatosis with polyangiitis presenting as livedo racemosa].
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2014As a rare antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis, eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss syndrome) is characterized by asthma, severe peripheral eosinophilia and the presence of extravascular granulomas.
N, Klossowski +6 more
openaire +1 more source
Livedo Racemosa: Clinical, Laboratory, and Histopathological Findings in 33 Patients
International Journal of Lower Extremity Wounds, 2021+2 more
exaly
Acral livedo racemosa after endovascular procedure
International Journal of Dermatology, 2019Juan Jimenez‐Cauhe +4 more
openaire +2 more sources
Biallelic variants in PROZ as a cause of hypercoagulability and livedo racemosa
Thrombosis Research, 2020Filippo, Pinto E Vairo +9 more
openaire +2 more sources
Livedo racemosa associated with central venous catheter use in a newborn
Pediatric Dermatology, 2023Tugba Bârsan Kaya +2 more
exaly
Bulletin de la Societe francaise de dermatologie et de syphiligraphie, 1969
P, Laugier +3 more
openaire +1 more source
P, Laugier +3 more
openaire +1 more source
Amantadine-Induced Livedo Racemosa
International Journal of Lower Extremity Wounds, 2016, Afsaneh Alavi, Mirian N Sotto
exaly