Results 101 to 110 of about 5,197,064 (280)
Cell-Free DNA and CXCL10 Derived from Bronchoalveolar Lavage Predict Lung Transplant Survival. [PDF]
Standard methods for detecting chronic lung allograft dysfunction (CLAD) and rejection have poor sensitivity and specificity and have conventionally required bronchoscopies and biopsies.
Damm, Izabella+11 more
core +2 more sources
Langerhans cell histiocytosis presented as bilateral otitis media and mastoiditis
Langerhans cell histiocytosis (LCH) is a rare disease that may affect multiple organs. The etiology of LCH remains unclear to date. It is currently believed that clonal accumulation and proliferation of CD1a-positive Langerhans cells are causative.
Charalampos E Skoulakis+5 more
doaj
Langerhans cell histiocytosis of the hip in children
Eight year old girl was referred to our consultation for a lameness with a flessum of the left hip with fever (38.5,C). Biology showed an inflammatory syndroma (CRP: 29 mg/l).
Zied Jlalia, Dhia Kaffel
doaj +1 more source
Rod-like tubular structures in the cytoplasm of histiocytes in “histiocytosis X” [PDF]
Jie Man
openalex +1 more source
Langerhans cell histiocytosis: Two clinical presentations in the same patient [PDF]
Langerhans cell histiocytosis (LCH) is a heterogeneous group of diseases characterized by a pathological proliferation of cells phenotypically similar to Langerhans cells.
Lobo, I.+4 more
core +1 more source
Ultrastructural examination of broncho-alveolar lavage for diagnosis of pulmonary histiocytosis X: Preliminary report on 4 cases. [PDF]
F Basset+3 more
openalex +1 more source
Langerhans’ cell histiocytosis diagnosed due to dermatological perianal lesion
Langerhans’ cell histiocytosis is a rare disease characterized by proliferation of Langerhans cells in the body. It affects mainly males, predominantly in childhood. Ulcerated plaques are one of the cutaneous forms of presentation.
Bruno Lorenzo Scolaro+5 more
doaj