Results 251 to 260 of about 55,121 (305)

Isolated Langerhans cell histiocytosis of the stomach in adults: An analysis of clinicopathologic characteristics and molecular genetics. [PDF]

Medicine (Baltimore)
Wu R, Zhao Y, Wu X, Gui H, Liu X, Liu Z.
europepmc   +1 more source

Two forced expiratory volume in 1 s trajectories with distinct prognoses in pulmonary Langerhans cell histiocytosis. [PDF]

ERJ Open Res
Benattia A, Porcher R, de Margerie-Mellon C, Caradec E, Lorillon G, Tazi A.   +5 more
europepmc   +1 more source

BRAF V600E mutation and high expression of PD-L1 in Rosai-Dorfman disease: case report and review of the literature. [PDF]

J Hematop
Moen FM, Youssef MM, Shukla M, Nierodzik ML, Mayerhoefer ME, Park C.   +5 more
europepmc   +1 more source

Histiocytosis of the orbit and its association with KRAS mutations. [PDF]

Blood Adv
Francis JH, Silverman RF, Canestraro J, Bossert D, Della Rocca D, Hatzoglou V, Abramson DH, Diamond EL.   +7 more
europepmc   +1 more source

[Hemophagocytic histiocytosis and medullary aplasia in typhoid fever].

, 1983
Valdés, M Ferrés, H Taboada
openalex  

Histiocytosis

The Lancet, 2021
Histiocytoses constitute a heterogeneous group of rare disorders, characterised by infiltration of almost any organ by myeloid cells with diverse macrophage or dendritic cell phenotypes. Histiocytoses can start at any age. Diagnosis is based on histology in combination with appropriate clinical and radiological findings.
Emile, Jean-François, Cohen-Aubart, Fleur, Collin, Matthew, Fraitag, Sylvie, Idbaih, Ahmed, Abdel-Wahab, Omar, Rollins, Barrett, Donadieu, Jean, Haroche, Julien   +8 more
openaire   +4 more sources

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Histiocitosis

Medicina Clínica, 2023
Histiocytosis is a group of rare diseases characterized by inflammation and accumulation of cells derived from monocytes and macrophages in different tissues. The symptoms are highly variable, from mild forms with involvement of a single organ to severe multisystem forms that can be life compromising.
Gemma, Rocamora-Blanch, Fina, Climent, Xavier, Solanich   +2 more
openaire   +2 more sources

FDG PET‐CT in pediatric Langerhans cell histiocytosis

Pediatric Blood & Cancer, 2020
Langerhans cell histiocytosis (LCH) in pediatric patients presents with single‐system or multisystem disease. Accurate staging is essential for selecting the most appropriate therapy ranging from local surgery to chemotherapy.
S. Jessop, Donna Crudgington, K. London, S. Kellie, R. Howman-Giles   +4 more
semanticscholar   +1 more source