Vascular Tumors and Malformations of the Ocular Fundus: Monographs in Ophthalmology, cartea 14
Autor J.J. de Laey, M. Hanssensen Limba Engleză Paperback – 28 sep 2011
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Specificații
ISBN-13: 9789401067539
ISBN-10: 9401067538
Pagini: 260
Ilustrații: 256 p.
Dimensiuni: 170 x 244 x 14 mm
Greutate: 0.42 kg
Ediția:Softcover reprint of the original 1st ed. 1990
Editura: SPRINGER NETHERLANDS
Colecția Springer
Seria Monographs in Ophthalmology
Locul publicării:Dordrecht, Netherlands
ISBN-10: 9401067538
Pagini: 260
Ilustrații: 256 p.
Dimensiuni: 170 x 244 x 14 mm
Greutate: 0.42 kg
Ediția:Softcover reprint of the original 1st ed. 1990
Editura: SPRINGER NETHERLANDS
Colecția Springer
Seria Monographs in Ophthalmology
Locul publicării:Dordrecht, Netherlands
Public țintă
ResearchCuprins
1. Choroidal Hemangioma.- I. Pathogenesis.- II. Clinical forms.- III. Symptoms.- IV. Complications.- IV. 1. Retinal complications.- V. Diagnosis.- VI. Histopathology.- VII. Treatment.- 2. Retinal Angiomatosis — von Hippel-Lindau’s Disease.- I. Pathogenesis.- II. Incidence.- III. Heredity.- IV. Ocular findings.- V. Associated neurological and visceral involvement or von Hippel-Lindau’s disease.- VI. Association of vHL disease with other diseases.- VI. 1. Association with other phakomatoses.- VII. Diagnosis.- VII. 1. Retinal angiomatosis.- VIII. Differential diagnosis.- IX. Pathology.- X. Treatment.- 3. Capillary Hemangioma of the Optic Disc.- I. Classification of angiomatous tumors of the optic disc.- II. Incidence.- III. Clinical features.- IV. Relationship with von Hippel-Lindau’s disease.- V. Diagnosis.- VI. Differential diagnosis.- VII. Histopathology.- VIII. Treatment.- 4. Cavernous Hemangioma of the Retina and of the Optic Disc.- I. Incidence.- II. Clinical features.- III. Systemic manifestations — Gass’ syndrome.- IV. Differential diagnosis.- V. Histopathology.- VI. Treatment.- 5. Congenital Arteriovenous Communications in the Retina.- I. Pathogenesis.- II. Heredity.- III. Incidence.- IV. Ocular manifestations.- V. Wyburn-Mason syndrome.- VI. Evolution of the retinal lesions.- VII. Histopathology.- VIII. Diagnosis.- IX. Differential diagnosis.- X. Treatment of the fundus lesions.- 6. Neurofibromatosis or von Recklinghausen’s Disease.- I. Pathogenesis.- II. Incidence and heredity.- III. Pathognomonic lesions.- IV. Fundus examinations in von Recklinghausen’Es disease.- V. Other ophthalmological manifestations.- VI. Association with other phakomatoses.- VII. Treatment.- 7. TUBEROUS SCLEROSIS.- I. Incidence and heredity.- II. Diagnostic criteria.- III.Non-ocular manifestations of tuberous sclerosis.- III. 1. Cutaneous manifestations.- IV. Ocular manifestations of tuberous sclerosis.- V. Associations.- 8. Congenital Retinal Telangiectasis.- I. Pathogenesis.- II. Incidence.- III. Heredity.- IV. Clinical aspects.- V. Associated conditions.- VI. Differential diagnosis.- VII. Histopathology.- VIII. Treatment.- 9. Idiopathic Juxtafoveolar Retinal Telangiectasis.- I. Incidence.- II. Heredity.- III. Clinical aspects.- IV. Differential diagnosis.- V. Histopathology.- VI. Pathogenesis.- VII. Treatment.- 10. Coats’ Syndrome and Retinitis Pigmentosa.- I. Incidence.- II. Clinical characteristics.- III. Differential diagnosis.- IV. Histopathology.- V. Pathogenesis.- VI. Treatment.- 11. Presumed Acquired Retinal Angiomatosis (Adult Coats’ Disease).- I. Incidence.- II. Clinical aspects.- III. Differential diagnosis.- IV. Histopathology.- V. Pathogenesis.- VI. Treatment.- 12. Acquired Retinal Macroaneurysms.- I. Incidence.- II. Clinical manifestations.- III. Associated diseases.- IV. Histopathology.- V. Pathogenesis.- VI. Differential diagnosis.- VII. Treatment.