Limit search to available items
Nearby Subjects are:
Result Page   Prev Next
Add Marked to Bag Add All On Page Add Marked to My Lists
Mark   Year Entries
 

Dystopia films -- See Dystopian films


  1
Dystopian : Ruben / Bruce Whatley  2017 1
 

Dystopian drama -- See Dystopian plays


  1
FICTION -- Dystopian.   2
Dystopian films.   7
Dystopian films -- History and criticism.   4
Dystopian philosophy : Nein. : a manifesto / Eric Jarosinski  2015 1
Dystopian plays.   16
 

Dystopias -- See Also Utopias


  1
Dystopias.   41
Dystopias -- Comic books, strips, etc   9
 

Dystopias Drama -- See Dystopian plays


  1
Dystopias -- Fiction   11
Dystopias -- History.   5
Dystopias in literature.   59
Dystopias in literature -- 20th century. : The memoirs of a survivor / Doris Lessing  1975 1
Dystopias in literature -- Handbooks, manuals, etc. : A reader's guide to George Orwell / Jeffrey Meyers  1975 1
Dystopias in literature -- History and criticism. : The Cambridge companion to utopian literature / edited by Gregory Claeys  2010 1
 

Dystopias Juvenile drama -- See Dystopian plays


  1
Dystopias -- Juvenile fiction.   33
Dystopias -- New York (State) -- New York -- Fiction. : Soylent green / presented by Metro-Goldwyn-Mayer ; produced by Walter Seltzer and Russell Thacher ; directed by Richard Fleischer ; screenplay by Stanley R. Greenberg  2003 1
Dystopias -- Pictorial works -- Juvenile fiction.   2
Dystopias -- Teen fiction : Catching fire / Suzanne Collins  2009 1
Dystopias -- Young adult fiction   3
 

Dystopic drama -- See Dystopian plays


  1
 

Dystopic plays -- See Dystopian plays


  1
 

Dystrophia mesodermalis congenita -- See Marfan syndrome


  1
  Dystrophia myotonica -- 2 Related Subjects   2
 

Dystrophia Myotonica 1 -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophia Myotonica 2 -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophia Myotonica 2s -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophia Myotonicas -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophica, Myotonia -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophicas, Myotonia -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophies, Congenital Myotonic -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophies, Corneal Granular -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
  1
 

Dystrophies, Corneal Macular -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
  1
 

Dystrophies, Corneal Stromal -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
  1
 

Dystrophies, Groenouw's -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
  1
 

Dystrophies, Hereditary Corneal -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
  1
 

Dystrophies, Macular -- See Macular Degeneration


Degenerative changes in the RETINA usually of older adults which results in a loss of vision in the center of the visual field (the MACULA LUTEA) because of damage to the retina. It occurs in dry and wet forms
  1
 

Dystrophies, Muscular -- See Muscular Dystrophies


A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS
  1
 

Dystrophies, Myotonic -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophies, Retinal -- See Retinal Dystrophies


A group of disorders involving predominantly the posterior portion of the ocular fundus, due to degeneration in the sensory layer of the RETINA; RETINAL PIGMENT EPITHELIUM; BRUCH MEMBRANE; CHOROID; or a combination of these tissues
  1
 

Dystrophin -- See Also Muscular Dystrophy, Duchenne


An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
  1
Dystrophin. : Duchenne muscular dystrophy / Jeff Chamberlain  2007 1
  Dystrophy -- 2 Related Subjects   2
 

Dystrophy, Congenital Myotonic -- See Myotonic Dystrophy


Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2
  1
 

Dystrophy, Corneal Granular -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
  1
 

Dystrophy, Corneal Macular -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
  1
Add Marked to Bag Add All On Page Add Marked to My Lists
Result Page   Prev Next