Zobrazeno 1 - 2
of 2
pro vyhledávání: '"MESH: Erdheim-Chester Disease"'
Autor:
Julien, Haroche, Yoram, Gueniche, Damien, Galanaud, Fleur, Cohen-Aubart, Didier, Dormont, Théophile, Rousseau, Zahir, Amoura, Valerie, Touitou, Natalia, Shor
Publikováno v:
Haematologica
Haematologica, 2022, 107 (11), pp.2667-2674. ⟨10.3324/haematol.2021.280510⟩
Haematologica, 2022, 107 (11), pp.2667-2674. ⟨10.3324/haematol.2021.280510⟩
International audience; Erdheim-Chester disease (ECD) is a rare L-group histiocytosis. Orbital involvement is found in a third of cases, but few data are available concerning the radiological features of ECD-related orbital disease (ECD-ROD). Our aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5deb2bfe8033a2f269b044f5ffdb0c7d
https://hal.science/hal-03891532
https://hal.science/hal-03891532
Autor:
Yaël Amar, Zahir Amoura, Neila Benameur, Jean-François Emile, Philippe Maksud, Fleur Cohen-Aubart, Damien Galanaud, Dorian Chauvet, Ahmed Idbaih, Julien Haroche
Publikováno v:
Neurology
Neurology, 2014, 83 (14), pp.1294-6. ⟨10.1212/WNL.0000000000000832⟩
Neurology, American Academy of Neurology, 2014, 83 (14), pp.1294-6. ⟨10.1212/WNL.0000000000000832⟩
Neurology, 2014, 83 (14), pp.1294-6. ⟨10.1212/WNL.0000000000000832⟩
Neurology, American Academy of Neurology, 2014, 83 (14), pp.1294-6. ⟨10.1212/WNL.0000000000000832⟩
Erdheim-Chester disease (ECD) is a rare non–Langerhans cell histiocytosis characterized by the accumulation of foamy CD68+CD1a− histiocytes. Tissue infiltration preferentially affects long bones and retroperitoneal and peri-aortic spaces, but alm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f9cb1578572354c8d3ca1ce7d702292
https://pubmed.ncbi.nlm.nih.gov/25171932
https://pubmed.ncbi.nlm.nih.gov/25171932
