Treatment of retinal capillary hemangioma.

[1]  C. Shields,et al.  Juxtapapillary capillary hemangiomas. Clinical features and visual acuity outcomes. , 2000, Ophthalmology.

[2]  K. Mireskandari,et al.  Transpupillary thermotherapy for retinal capillary hemangioma in von Hippel-Lindau disease. , 2000, Ophthalmic surgery and lasers.

[3]  H. Neumann,et al.  Long-term results of laser treatment for retinal angiomatosis in von Hippel-Lindau disease. , 2000, European journal of medical research.

[4]  J. Weitzel.  Genetic cancer risk assessment , 1999, Cancer.

[5]  A. Webster,et al.  Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation. , 1999, Archives of ophthalmology.

[6]  N. Bornfeld,et al.  Ruthenium-106 brachytherapy for peripheral retinal capillary hemangioma. , 1998, Ophthalmology.

[7]  P. Choyke,et al.  von Hippel-Lindau disease: genetic, clinical, and imaging features. , 1995, Radiology.

[8]  Lloyd M. Smith,et al.  Statement on use of DNA testing for presymptomatic identification of cancer risk. National Advisory Council for Human Genome Research. , 1994, JAMA.

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

[10]  J. Shields.  Response of retinal capillary hemangioma to cryotherapy. , 1993, Archives of ophthalmology.

[11]  M. Gorin.  Von Hippel-Lindau disease: clinical considerations and the use of fluorescein-potentiated argon laser therapy for treatment of retinal angiomas. , 1992, Seminars in ophthalmology.

[12]  C. Shields,et al.  von Hippel-Lindau disease. , 2001, Survey of ophthalmology.

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

[14]  J. Folk,et al.  Direct and feeder vessel photocoagulation of retinal angiomas with dye yellow laser. , 1990, Ophthalmology.

[15]  I. Kremer,et al.  Juxtapapillary exophytic retinal capillary hemangioma treated by yellow krypton (568 nm) laser photocoagulation. , 1988, Ophthalmic surgery.

[16]  J. Williams,et al.  Pathogenesis and therapy of traction detachment in various retinal vascular diseases. , 1988, American journal of ophthalmology.

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

[18]  J. Gass,et al.  Sessile and exophytic capillary angiomas of the juxtapapillary retina and optic nerve head. , 1980, Archives of ophthalmology.

[19]  R. Carr,et al.  7. Retinal Angiomatosis , 1980 .

[20]  J. Lamiell,et al.  Early identification of retinal angiomas in a large kindred von Hippel-Lindau disease. , 1980, American journal of ophthalmology.

[21]  Gass Jd.  Treatment of retinal vascular anomalies. , 1977 .

[22]  W. Tasman,et al.  Fifteen year review of treated cases of retinal angiomatosis. , 1977, Transactions. Section on Ophthalmology. American Academy of Ophthalmology and Otolaryngology.

[23]  L. Sarin,et al.  Hemangiomas of the optic disc. , 1975, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

[24]  R. Watzke.  Cryotherapy for retinal angiomatosis. A clinicopathologic report. , 1974, Archives of ophthalmology.

[25]  M. Goldberg,et al.  Argon laser treatment of von Hippel-Lindau retinal angiomas. I. Clinical and angiographic findings. , 1974, Archives of ophthalmology.

[26]  J. Oosterhuis,et al.  Haemangioma at the optic disc. , 1971, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.

[27]  T. Smith,et al.  Cryotherapy of angiomatosis retinae. , 1969, Archives of ophthalmology.

[28]  W. Hoyt,et al.  Incipient lesions of von Hippel-Lindau disease. , 1968, Archives of ophthalmology.

[29]  K. Melmon,et al.  Lindau's disease: Review of the literature and study of a large kindred , 1964 .

[30]  F. Mcgovern,et al.  Diathermy Coagulation in the Treatment of Angiomatosis Retinae and of Juvenile Coats's Disease: Report of Two Cases* , 1943 .

[31]  W. Linehan,et al.  Improved detection of germline mutations in the von Hippel‐Lindau disease tumor suppressor gene , 1998, Human mutation.

[32]  E. Gragoudas,et al.  Advances in Treatment of Retinal Angiomas , 1997, International ophthalmology clinics.

[33]  M. J. Kahn,et al.  Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consent. , 1997, JAMA.

[34]  H. Flynn,et al.  Pars plana vitrectomy and direct diathermy for complications of multiple retinal angiomas. , 1992, Ophthalmic surgery.

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

[36]  Hsia Ye,et al.  von Hippel-Lindau disease affecting 43 members of a single kindred. , 1989 .

[37]  A. Bird,et al.  Laser treatment of retinal angiomatosis , 1989, Eye.

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

[39]  M. Bonnet,et al.  [Treatment of retinal capillary angiomas of von Hippel's disease]. , 1984, Journal francais d'ophtalmologie.

[40]  R. Welch,et al.  Von Hippel-Lindau disease: the recognition and treatment of early angiomatosis retinae and the use of cryosurgery as an adjunct to therapy. , 1970, Transactions of the American Ophthalmological Society.

[41]  A. Schwartz,et al.  Angiomatosis retinae, von Hippel's disease, eleven years after irradiation. , 1952, Transactions of the American Ophthalmological Society.

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