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Retinene -- See Retinal (Visual pigment)


  1
Retinger, J. H. (Joseph Hieronim), 1888-1960.   2
 

Retinger, Joseph Hieronim, 1888-1960 -- See Retinger, J. H. (Joseph Hieronim), 1888-1960


  1
 

Retinger, Józef H., 1888-1960 -- See Retinger, J. H. (Joseph Hieronim), 1888-1960


  1
Retinitis Pigmentosa.   6
Retinitis pigmentosa -- Congresses. : Retinitis pigmentosa : clinical implications of current research / edited by Maurice B. Landers, III ... [and others]  1977 1
Retinitis Pigmentosa -- diagnosis. : Retinitis pigmentosa : causes, diagnosis and treatment / Michaël Baert and Cédric Peeters, editors  2010 1
Retinitis Pigmentosa -- etiology. : Retinitis pigmentosa : causes, diagnosis and treatment / Michaël Baert and Cédric Peeters, editors  2010 1
Retinitis pigmentosa -- Patients. : 60 Minutes: Race For Life/Seeing is Believing/Charlie's Fightback  2015 1
Retinitis pigmentosa -- Patients -- Australia. : Love-heart baby / written and directed by Shalom Almond  2012 1
Retinitis pigmentosa -- Patients -- Biography. : Cockeyed : a memoir / Ryan Knighton  2006 1
Retinitis Pigmentosa -- therapy. : Retinitis pigmentosa : causes, diagnosis and treatment / Michaël Baert and Cédric Peeters, editors  2010 1
Retinoblastoma.   8
Retinoblastoma -- diagnosis   2
 

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)
  1
 

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)
  1
 

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)
  1
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)
  1
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)
  1
 

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)
  1
 

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)
  1
 

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)
  1
 

Retinoic acid receptors -- See Tretinoin Receptors


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Rétinoïdes -- usage thérapeutique. : Retinoids and carotenoids in dermatology / edited by Anders Vahlquist, Madeleine Duvic  2007 1
  Retinoids -- 2 Related Subjects   2
Retinoids.   5
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
  1
 

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
  1
 

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
  1
 

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
  1
 

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
  1
 

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
  1
 

Retinopathy of prematurity -- See Retrolental fibroplasia


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Retinopathy of Prematurity -- diagnosis : Retinopathy of prematurity : current diagnosis and management / B. Andrés Kychenthal, S. Paola Dorta, editors  2017 1
Retinopathy of Prematurity -- therapy : Retinopathy of prematurity : current diagnosis and management / B. Andrés Kychenthal, S. Paola Dorta, editors  2017 1
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