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Lung, 1985
Pulmonary histiocytosis X is a granulomatous disorder of the lung of unknown cause. Patients with this disease often complain of cough, dyspnea on exertion, and, occasionally, chest pain from a pneumothorax or bone involvement. However, it is not unusual for patients to be asymptomatic with only a diffuse interstitial infiltrate on their chest ...
T W, Marcy, H Y, Reynolds
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Pulmonary histiocytosis X is a granulomatous disorder of the lung of unknown cause. Patients with this disease often complain of cough, dyspnea on exertion, and, occasionally, chest pain from a pneumothorax or bone involvement. However, it is not unusual for patients to be asymptomatic with only a diffuse interstitial infiltrate on their chest ...
T W, Marcy, H Y, Reynolds
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Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina, 1996
Histiocytosis X comprises a spectrum of diseases of unknown etiology in which localized or systemic histiocytic proliferations occur, often associated with eosinophilic infiltration of the involved tissues. The three clinical syndromes are: eosinophilic granuloma, Hand-Schuller-Christian disease and Abta-Letteres-Siwesche's disease.
L, Grzybowska, P, Tutka
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Histiocytosis X comprises a spectrum of diseases of unknown etiology in which localized or systemic histiocytic proliferations occur, often associated with eosinophilic infiltration of the involved tissues. The three clinical syndromes are: eosinophilic granuloma, Hand-Schuller-Christian disease and Abta-Letteres-Siwesche's disease.
L, Grzybowska, P, Tutka
openaire +1 more source
BRAFV600E-induced senescence drives Langerhans cell histiocytosis pathophysiology
Nature Medicine, 2021Camille Bigenwald +2 more
exaly