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Dystonias, Secondary -- See Dystonic Disorders


Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset
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Dystonias, Sporadic -- See Dystonic Disorders


Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset
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Dystonias, Torsion -- See Dystonia Musculorum Deformans


A condition characterized by focal DYSTONIA that progresses to involuntary spasmodic contractions of the muscles of the legs, trunk, arms, and face. The hands are often spared, however, sustained axial and limb contractions may lead to a state where the body is grossly contorted. Onset is usually in the first or second decade. Familial patterns of inheritance, primarily autosomal dominant with incomplete penetrance, have been identified. (Adams et al., Principles of Neurology, 6th ed, p1078)
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Dystonic Disorder -- See Dystonic Disorders


Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset
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Dystonic Disorders -- See Also Dystonia


An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77)
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Dystonic Disorders.   4
Dystonic Disorders -- diagnosis : Clinical diagnosis and management of dystonia / edited by Thomas T. Warner, Susan B. Bressman  2007 1
Dystonic Disorders -- therapy : Clinical diagnosis and management of dystonia / edited by Thomas T. Warner, Susan B. Bressman  2007 1
 

Dystonic-Rigid Cerebral Palsies -- See Cerebral Palsy


A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
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Dystonic-Rigid Cerebral Palsy -- See Cerebral Palsy


A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7)
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Dystopia films -- See Dystopian films


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Dystopian : Ruben / Bruce Whatley  2017 1
 

Dystopian drama -- See Dystopian plays


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Dystopian fiction : Boy and his dog at the end of the world / C. A. Fletcher  2019 1
Dystopian films.   8
Dystopian films -- History and criticism.   6
Dystopian philosophy : Nein. : a manifesto / Eric Jarosinski  2015 1
Dystopian plays.   17
 

Dystopias -- See Also Utopias


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Dystopias.   47
 

Dystopias Drama -- See Dystopian plays


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Dystopias -- Fiction   16
Dystopias -- History.   5
Dystopias in literature.   75
Dystopias in literature -- 20th century. : The memoirs of a survivor / Doris Lessing  1975 1
Dystopias in literature -- Congresses : ICONOFAGIAS, DISTOPIAS Y FARSAS : ficcion y politica en america latina    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


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Dystopias -- Juvenile fiction.   32
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


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Dystopic plays -- See Dystopian plays


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Dystrophia mesodermalis congenita -- See Marfan syndrome


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  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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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