Histogenesis of haemangioblastomas: an immunocytochemical and ultrastructural study in a case of von Hippel-Lindau syndrome.

Author:

Ismail S M,Jasani B,Cole G

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference24 articles.

1. Familial islet cell tumours in von Hippel-Lindau's disease;Hull, M.T.; Wastel, K.A.; Muller, J.; Higgins, J.T.;Cancer,1979

2. Von Hippel-Lindau's disease, syringomyelia and multiple endocrine tumours: A complex neuroendocrinopathy;Probst, A.; Lotz, M.; Heitz, P.L.;Virchows Arch [Al Pathol Anat,1978

3. Von Hippel-Lindau disease. Clinical and pathological manifestations in nine families with 50 affected members;Hoston, W.A.; Wong, V.; Eldridge, R.;Arch Intern Med,1976

4. Lindau's disease. Review of the literature and study of a large kindred;Melmon, K.L.; Rosen, S.W.;Am J Med,1964

5. Cerebellar haemangioma (haemangioblastoma). A clinico-pathological review of 40 cases;G, Silver M.L.Hennigar;J Neurosurg; Haemangioblastomas: histogenesis of the stromal cell studied by immunocytochemistry,1952

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