The eye in von Hippel–Lindau disease. Long‐term follow‐up of screening and treatment: recommendations

Wittebol‐Post D, Hes FJ, Lips CJM (University Hospital Utrecht, Utrecht, The Netherlands). The eye in von Hippel–Lindau disease. Long‐term follow‐up of screening and treatment: recommendations (Minisymposium: MEN & VHL). J Intern Med 1998; 243: 555–561.

[1]  V. Couch,et al.  von Hippel-Lindau disease. , 2000, Mayo Clinic proceedings.

[2]  Christopher A. Friedrich Von Hippel‐Lindau Syndrome , 1999 .

[3]  K. Plate,et al.  Pathology, genetics and cell biology of hemangioblastomas. , 1996, Histology and histopathology.

[4]  A. Webster,et al.  Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations. , 1996, Journal of medical genetics.

[5]  R. Whitehouse,et al.  A genetic register for von Hippel-Lindau disease. , 1996, Journal of medical genetics.

[6]  B. Ponder,et al.  Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma. , 1995, Journal of medical genetics.

[7]  A. Webster,et al.  Clinical features and molecular genetics of Von Hippel-Lindau disease. , 1995, Ophthalmic genetics.

[8]  J. Gnarra,et al.  Identification of the von Hippel-Lindau disease tumor suppressor gene. , 1993, Science.

[9]  H. Grossniklaus,et al.  Retinal Hemangioblastoma: A Histologic, Immunohistochemical, and Ultrastructural Evaluation , 1992 .

[10]  A. Bird,et al.  Ophthalmological screening for von Hippel-Lindau disease , 1991, Eye.

[11]  M. Ferguson-Smith,et al.  Clinical features and natural history of von Hippel-Lindau disease. , 1990, The Quarterly journal of medicine.

[12]  J. Haines,et al.  Von Hippel–Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma , 1988, Nature.

[13]  V. Michels Chapter 4 – Von Hippel–Lindau Disease , 1987 .

[14]  R. Welch,et al.  VON HIPPEL‐LINDAU DISEASE: Case Report of a Patient with Spontaneous Regression of a Retinal Angioma , 1986, Retina.

[15]  D. Robertson,et al.  von Hippel-Lindau disease: a familial, often lethal, multi-system phakomatosis. , 1984, Ophthalmology.

[16]  L. Rossant [The phakomatoses]. , 1977, L'Infirmiere francaise.

[17]  W. Green,et al.  Light and electron microscopic study of early lesions in angiomatosis retinae. , 1976, American journal of ophthalmology.

[18]  M. Goldberg,et al.  Argon laser treatment of von Hippel-Lindau retinal angiomas. II. Histopathology of treated lesions. , 1974, Archives of ophthalmology.

[19]  A. Lindau Studien Uber Kleinhirncysten. Bau, Pathogenese und Beziehungen zur Angiomatosis Retinae , 1926 .