Reactivation of Hand-Schüller-Christian disease six and thirteen years after discontinuation of systemic therapy.
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[1] D. Sims. Histiocytosis X; follow-up of 43 cases. , 1977, Archives of disease in childhood.
[2] W. Zinkham. Multifocal eosinophilic granuloma. Natural history, etiology and management. , 1976, The American journal of medicine.
[3] M. Lahey,et al. Histiocytosis x--an analysis of prognostic factors. , 1975, The Journal of pediatrics.
[4] J. Vogel,et al. Idiopathic histiocytosis: a discussion of eosinophilic granuloma, the Hand-Schüller-Christian syndrome, and the Letterer-Siwe syndrome. , 1972, Seminars in hematology.
[5] Judy I. Henderson. HISTIOCYTIC RETICULOSIS: A REVIEW OF 20 PATIENTS IN THE PÆDIATRIC AGE RANGE , 1969, The Medical journal of Australia.
[6] P. Lieberman,et al. A REAPPRAISAL OF EOSINOPHILIC GRANULOMA OF BONE, HAND‐SGHÜLLER‐CHRISTIAN SYNDROME AND LETTERER‐SIWE SYNDROME , 1969, Medicine.
[7] D. Dahlin,et al. Histiocytosis X: a clinical study. , 1967, Mayo Clinic proceedings.
[8] M. Lahey. Prognosis in reticuloendotheliosis in children , 1962 .
[9] H. Oberman. IDIOPATHIC HISTIOCYTOSIS A Clinicopathologic Study of 40 Cases and Review of the Literature on Eosinophilic Granuloma of Bone, Hand-Schüller-Christian Disease and Letterer-Siwe Disease , 1961 .
[10] M. Avery,et al. The course and prognosis of reticuloendotheliosis (eosinophilic granuloma, Schüller-Christian disease and Letterer-Siwe disease); a study of forty cases. , 1957, The American journal of medicine.