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Spinocerebellar Ataxia Proteins -- See Ataxins


A family of predominantly nuclear proteins that regulate gene transcription and protein degradation. The expansion of CAG trinucleotide repeats in genes that encode Ataxins is associated with SPINOCEREBELLAR ATAXIAS (SCA). In SCA patients, the number of CAG repeats correlates with the severity of disease and inversely correlates with the age of disease onset
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Spinocerebellar Ataxia Type 1 -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Ataxia Type 2 -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Ataxia Type 4 -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Ataxia Type 5 -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Ataxia Type 6 -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Ataxia Type 7 -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Ataxia with Slow Eye Movements -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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  Spinocerebellar Ataxias -- 2 Related Subjects   2
 

Spinocerebellar Ataxias, Dominantly-Inherited -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophies -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophy -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophy 2 -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophy 2s -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophy I -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophy II -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophy IIs -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Atrophy Is -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar degeneration -- See Friedreich's ataxia


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Spinocerebellar Degeneration with Slow Eye Movements -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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Spinocerebellar Degenerations -- diagnosis. : Handbook of ataxia disorders / edited by Thomas Klockgether  2000 1
Spinocerebellar Degenerations -- therapy. : Handbook of ataxia disorders / edited by Thomas Klockgether  2000 1
 

Spinoffs, Corporate -- See Corporate divestiture


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Spinola, Ambrogio, 1569-1630. : Ambrogio Spinola between Genoa, Flanders, and Spain / edited by Silvia Mostaccio, Bernardo J. García García, Luca Lo Basso  2022 1
 

Spinopontine Atrophies -- See Muscular Disorders, Atrophic


Disorders characterized by an abnormal reduction in muscle volume due to a decrease in the size or number of muscle fibers. Atrophy may result from diseases intrinsic to muscle tissue (e.g., MUSCULAR DYSTROPHY) or secondary to PERIPHERAL NERVOUS SYSTEM DISEASES that impair innervation to muscle tissue (e.g., MUSCULAR ATROPHY, SPINAL)
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Spinopontine Atrophy -- See Muscular Disorders, Atrophic


Disorders characterized by an abnormal reduction in muscle volume due to a decrease in the size or number of muscle fibers. Atrophy may result from diseases intrinsic to muscle tissue (e.g., MUSCULAR DYSTROPHY) or secondary to PERIPHERAL NERVOUS SYSTEM DISEASES that impair innervation to muscle tissue (e.g., MUSCULAR ATROPHY, SPINAL)
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  Spinor analysis -- 2 Related Subjects   2
Spinor analysis.   14
 

Spinor calculus -- See Spinor analysis


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Spinoranalysis : Clifford algebras and spinors / Pertti Lounesto  2001 1
 

Spinors, Theory of -- See Spinor analysis


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Spinosaurus. : Bigger Than T-Rex / Director: Cohen, Chad  2014 1
Spinoza. : The infinite / A.W. Moore  2019 1
 

Spinoza, Baruch, 1632-1677 -- See Spinoza, Benedictus de, 1632-1677


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Spinoza, Baruch de, 1632-1677 -- See Spinoza, Benedictus de, 1632-1677


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Spinoza, Barukh, 1632-1677 -- See Spinoza, Benedictus de, 1632-1677


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Spinoza, Benedict de, 1632-1677 -- See Spinoza, Benedictus de, 1632-1677


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Spinoza, Benedictus de, 1622-1677 -- Criticism and interpretation : SPINOZA. EDUCACION PARA EL CAMBIO  2018 1
Spinoza, Benedictus de, 1632-1677.   167
Spinoza, Benedictus de, 1632-1677., Benedictus de : Studies in Spinoza, critical and interpretive essays. / Edited by S. Paul Kashap  1972 1
Spinoza, Benedictus de, 1632-1677 -- Bibliography.   2
Spinoza, Benedictus de, 1632-1677 -- Censorship : Spinoza, life and legacy / Jonathan I. Israel  2023 1
Spinoza, Benedictus de, 1632-1677 -- Congresses.   5
Spinoza, Benedictus de, 1632-1677 -- Contributions in concept of expression : Expressionism in philosophy : Spinoza / Gilles Deleuze ; translated by Martin Joughin  1992 1
Spinoza, Benedictus de, 1632-1677 -- Contributions in concept of responsibility : Collective imaginings : Spinoza, past and present / Moira Gatens and Genevieve Lloyd  2002 1
Spinoza, Benedictus de, 1632-1677 -- Contributions in philosophy of imagination : Collective imaginings : Spinoza, past and present / Moira Gatens and Genevieve Lloyd  2002 1
Spinoza, Benedictus de, 1632-1677 -- Correspondence. : The collected works of Spinoza / edited and translated by Edwin Curley  c1985- 1
Spinoza, Benedictus de, 1632-1677 -- Criticism and interpretation   10
Spinoza, Benedictus de, 1632-1677 -- Drama   2
 

Essence of Spinoza's Ethics -- See Ethica. English


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