Results 101 to 110 of about 10,973 (224)

LGL-leukemia ja autoimmuniteetti : autoimmuunisairauden ja syövän rajapinta hämärtyy [PDF]

open access: yes, 2016
English summaryPeer ...
Mustjoki, Satu   +2 more
core  

[Hypergammaglobulinemia D syndrome].

open access: yesAnales de medicina interna (Madrid, Spain : 1984), 2000
The hyperimmunoglobulinemia D syndrome is characterized by early onset of attacks of periodic fever and an elevated serum polyclonal Ig D (> 100 U/ml). Symptoms during attacks include joint involvements (arthralgia/arthritis), skin lesions, swollen lymph nodes, headache and abdominal complaints (vomiting, diarrhea and pain).
M, Medrano San Ildefonso, C, Bruscas Izu
openaire   +1 more source

Reciprocal expression of interferon gamma or interleukin 4 during the resolution or progression of murine leishmaniasis. Evidence for expansion of distinct helper T cell subsets. [PDF]

open access: yes, 1989
We purified poly(A)+ mRNA from the spleen and lymph nodes at designated times after infection with Leishmania major in genetically susceptible BALB/c and resistant C57BL/6 mice.
Coffman, RL   +4 more
core  

Case Report: two cases of idiopathic plasmacytic lymphadenopathy subtype of idiopathic multicentric Castleman disease with xanthelasma palpebrum from a Canadian center

open access: yesFrontiers in Hematology
BackgroundIdiopathic plasmacytic lymphadenopathy is a newly recognized subtype of idiopathic multicentric Castleman disease (iMCD-IPL) and often mimics IgG4-related disease (IgG4-RD).
Andrew A. Y. Chen   +12 more
doaj   +1 more source

Erythrocyte Antibodies in AIDS are associated with mycobacteriosis and hypergammaglobulinemia [PDF]

open access: yes, 1990
A. Matuschke   +21 more
core   +1 more source

Bone Marrow Negative Visceral Leishmaniasis in an Adolescent Male

open access: yesIranian Journal of Parasitology, 2013
Visceral Leishmaniasis or Kala Azar is endemic in certain regions of India. In endemic areas, the constella­tion of fever, progressive weight loss, weakness, pronounced splenomegaly, anemia, leukope­nia, and hypergammaglobulinemia is highly suggestive of
S Jetley   +5 more
doaj   +2 more sources

Eosinophilic Fasciitis: A Review of Research and Therapeutic Possibilities

open access: yesJournal of Education, Health and Sport
Introduction Eosinophilic fasciitis (EF) is a rare inflammatory disorder marked by elevated eosinophils in tissues and blood. Patients typically present with symptoms such as skin swelling, pain, and induration, which can be mistaken for other ...
Julia Biernikiewicz   +9 more
doaj   +1 more source

Increased serum levels of macrophage migration inhibitory factor in patients with primary Sjögren's syndrome [PDF]

open access: yes, 2007
Peter Willeke   +6 more
core   +1 more source

Rituximab-induced serum sickness: Not so uncommon

open access: yesIndian Journal of Rheumatology, 2018
Vikramraj K Jain
doaj   +1 more source

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