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Retinoblastoma Eye Cancer -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastoma Eye Cancers -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastoma, Familial -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastoma, Hereditary -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastoma -- pathology. : Ocular oncology / edited by Daniel M. Albert, Arthur Polans  2003 1
Retinoblastoma Protein -- physiology. : Rb and tumorigenesis / [edited by] Maurizio Fanciulli  2006 1
 

Retinoblastoma, Sporadic -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastoma -- therapy.   3
Retinoblastoma -- Treatment.   2
 

Retinoblastomas -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastomas, Familial -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastomas, Hereditary -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoblastomas, Sporadic -- See Retinoblastoma


A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)
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Retinoic acid receptors -- See Tretinoin Receptors


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  Retinoids -- 2 Related Subjects   2
Retinoids.   4
Retinoids -- Health aspects. : Carotenoids and retinoids : molecular aspects and health issues / editors, Lester Packer [and others]  2005 1
Retinoids -- Molecular aspects. : Carotenoids and retinoids : molecular aspects and health issues / editors, Lester Packer [and others]  2005 1
Retinoids -- Periodicals. : Clinical dermatology    1
Retinoids -- pharmacology.   2
Retinoids -- Physiological effect.   2
Retinoids -- Physiological effect -- Congresses. : Retinoids, advances in basic research and therapy : proceedings of the International Dermatology Symposion (IDS), Berlin, October 13-15, 1980 / edited by C.E. Orfanos and O. Braun-Falco ... [and others]  1981 1
Retinoids -- therapeutic use.   4
Retinoids -- Therapeutic use -- Periodicals. : Clinical dermatology    1
  Retinol -- 2 Related Subjects   2
 

Retinopathies, Cancer-Associated -- See Paraneoplastic Syndromes, Ocular


Ocular manifestations secondary to various NEOPLASMS in which antibodies to antigens of the primary tumor cross-react with ocular antigens. This autoimmune response often leads to visual loss and other ocular dysfunctions
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Retinopathies, Diabetic -- See Diabetic Retinopathy


Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION
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Retinopathies, Melanoma-Associated -- See Paraneoplastic Syndromes, Ocular


Ocular manifestations secondary to various NEOPLASMS in which antibodies to antigens of the primary tumor cross-react with ocular antigens. This autoimmune response often leads to visual loss and other ocular dysfunctions
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Retinopathies, Pigmentary -- See Retinitis Pigmentosa


Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina
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Retinopathy, Cancer-Associated -- See Paraneoplastic Syndromes, Ocular


Ocular manifestations secondary to various NEOPLASMS in which antibodies to antigens of the primary tumor cross-react with ocular antigens. This autoimmune response often leads to visual loss and other ocular dysfunctions
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Retinopathy, Diabetic -- See Diabetic Retinopathy


Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION
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Retinopathy, Melanoma-Associated -- See Paraneoplastic Syndromes, Ocular


Ocular manifestations secondary to various NEOPLASMS in which antibodies to antigens of the primary tumor cross-react with ocular antigens. This autoimmune response often leads to visual loss and other ocular dysfunctions
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Retinopathy of prematurity -- See Retrolental fibroplasia


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Retinopathy, Pigmentary -- See Retinitis Pigmentosa


Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina
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Retinoschisis -- See Also Retinal Detachment


Separation of the inner layers of the retina (neural retina) from the pigment epithelium. Retinal detachment occurs more commonly in men than in women, in eyes with degenerative myopia, in aging and in aphakia. It may occur after an uncomplicated cataract extraction, but it is seen more often if vitreous humor has been lost during surgery. (Dorland, 27th ed; Newell, Ophthalmology: Principles and Concepts, 7th ed, p310-12)
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Retinoscopy -- See Also Refraction, Ocular


Refraction of LIGHT effected by the media of the EYE
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Retired air force personnel -- See Retired military personnel



--subdivision Appointments and retirements under armies and navies, e.g. United States. Army--Appointments and retirements
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Retired army personnel -- See Retired military personnel



--subdivision Appointments and retirements under armies and navies, e.g. United States. Army--Appointments and retirements
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Retired engineers. : Space Cowboys (Movie 2000) / Director: Eastwood, Clint  2019 1
Retired executives -- Fiction. : The Philanthropist / John Tesarsch  2010 1
 

Retired government officials and employees -- See Civil service pensioners



--subdivision Officials and employees, Retired under countries, cities, etc
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Retired member of the detective police -- See Russell, William


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Retired military officers -- See Retired military personnel



--subdivision Appointments and retirements under armies and navies, e.g. United States. Army--Appointments and retirements
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Retired military personnel -- See Also Veterans



--subdivision Veterans under individual wars, e.g. World War, 1939-1945--Veterans
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Retired military personnel.   4
Retired military personnel -- Australia -- Biography. : As luck would have it : the reminiscences of an Australian sailor / by Sir John Collins  1965 1
Retired military personnel -- Employment.   2
Retired military personnel -- Employment -- Africa, Sub-Saharan : Civilian skills for African military officers to resolve the infrastructure, economic development, and stability crisis in Sub-Saharan Africa / Diane E. Chido  2011 1
Retired military personnel -- Employment -- United States.   5
Retired military personnel -- Employment -- United States -- History -- 20th century. : Soldiers to citizens : the G.I. bill and the making of the greatest generation / Suzanne Mettler  2005 1
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