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Retinal Vein Occlusion -- therapy -- Handbooks : Management of retinal vein occlusion : current concepts / editor, Seenu M. Hariprasad ; section editors Sophie J. Bakri, MD [and five others]  2014 1
 

Retinal Vessel -- See Retinal Vessels


The blood vessels which supply and drain the RETINA
  1
 

Retinal Vessels -- See Also Fluorescein Angiography


Visualization of a vascular system after intravenous injection of a fluorescein solution. The images may be photographed or televised. It is used especially in studying the retinal and uveal vasculature
  1
Retinal Vessels   4
Retinal Vessels -- diagnostic imaging   3
Retinal Vessels -- pathology : Retinal vascular disease / A.M. Joussen [and others] (eds)  2007 1
  Retinal (Visual pigment) -- 3 Related Subjects   3
Retinal (Visual pigment) -- Hemorrhage : Management of Macular Hemorrhage / edited by Lars-Olof Hattenbach  2018 1
 

Retinaldehyde -- See Retinal (Visual pigment)


  1
 

Retinas -- See Retina


The ten-layered nervous tissue membrane of the eye. It is continuous with the OPTIC NERVE and receives images of external objects and transmits visual impulses to the brain. Its outer surface is in contact with the CHOROID and the inner surface with the VITREOUS BODY. The outer-most layer is pigmented, whereas the inner nine layers are transparent
  1
Rétine -- Dégénérescence. : Retinal degenerative diseases / edited by Joe G. Hollyfield, Richard E. Anderson, Matthew M. LaVail  2006 1
Rétine -- Dégénérescence -- Traitement. : Retinal degenerative diseases / edited by Joe G. Hollyfield, Richard E. Anderson, Matthew M. LaVail  2006 1
 

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 -- Genetic aspects : Retinitis pigmentosa / edited by Stephen H. Tsang, Peter M.J. Quinn  2023 1
Retinitis pigmentosa -- Patients   2
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 -- Patients -- Canada -- Biography : Beyond vision : going blind, inner seeing, and the nature of the self / Allan Jones  2018 1
Retinitis Pigmentosa -- therapy : Retinitis pigmentosa : causes, diagnosis and treatment / Michaël Baert and Cédric Peeters, editors  2010 1
Retinitis pigmentosa -- Treatment : Retinitis pigmentosa / edited by Stephen H. Tsang, Peter M.J. Quinn  2023 1
Retinoblastoma   10
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)
  1
 

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 -- Laboratory manuals : The retinoblastoma protein / edited by Pedro G. Santiago-Cardona  2018 1
Retinoblastoma -- pathology : Ocular oncology / edited by Daniel M. Albert, Arthur Polans  2003 1
Retinoblastoma Protein : The retinoblastoma protein / edited by Pedro G. Santiago-Cardona  2018 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


  1
Rétinoïdes -- usage thérapeutique. : Retinoids and carotenoids in dermatology / edited by Anders Vahlquist, Madeleine Duvic  2007 1
  Retinoids -- 2 Related Subjects   2
Retinoids.   9
Retinoids -- Analysis : Retinoid protocols / edited by Christopher P.F. Redfern  1998 1
Retinoids -- Analysis -- Laboratory manuals : Retinoid protocols / edited by Christopher P.F. Redfern  1998 1
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