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Atari (U.S.) Corp.   2
Atari (U.S.) Corp. -- History : Atari design : impressions on coin-operated video game machines / Raiford Guins (author)  2021 1
 

Atari VCS (Video game console) -- See Atari 2600 (Video game console)


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Atari video computer system -- See Atari 2600 (Video game console)


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Ataris (Musical group) / http://id.loc.gov/authorities/names/n2002076757 : Contemporary musicians. Volume 62 : profiles of the people in music / Andrea Henderson, project editor  2008 1
Atarshchikov, Semën, 1807-1845. : Bitter choices : loyalty and betrayal in the Russian conquest of the North Caucasus / Michael Khodarkovsky  2011 1
 

ATAS/UCLA Television Archives -- See Also UCLA Film and Television Archive


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Atashin, Faegheh -- See Googoosh


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ATÄT -- See Organization for Security and Co-operation in Europe


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Atati͡urk, Kemalʹ, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atati͡urk, Mustafa Kemal, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atatourk, Moustapha Kemal, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atatsi͡urk, Mustafa Kemalʹ, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atatu̇rīk, Mustafa Kemal, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atātūrk, Kamāl, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atatürk, Kemal, 1881-1938   19
Atatürk, Kemal, 1881-1938 -- Biography. : Dromkeen : a journey into children's literature / Jeffrey Prentice and Bettina Bird  1988 1
Atatürk, Kemal, 1881-1938 -- Knowledge and learning : Atatürk : an intellectual biography / M. Şükrü Hanioğlu  2011 1
Atatürk, Kemal, 1881-1938 -- Musical settings : Symphony no. 2 : "Gallipoli - the 57th Regiment" / Can Atilla  2017 1
Atatürk, Kemal, 1881-1938 -- Nutuk : Crafting Turkish National Identity, 1919-1927 A Rhetorical Approach  2021 1
Atatürk, Kemal, 1881-1938 -- Political and social views   3
 

Atatürk, Mustafa Kamal, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atatürk, Mustafa Kemal, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Ataturk, Mustapha Kemal, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Ataturkism -- See Kemalism


Here are entered works on the political, economic and social principles advocated by Kemal Ataturk designed to create a modern republican secular Turkish state
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Ataturku, Mustafa Qemal, 1881-1938 -- See Atatürk, Kemal, 1881-1938


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Atava (Ont.) -- See Ottawa (Ont.)


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Atavism -- See Also Heredity


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Atavism   2
Atavism -- History -- 19th century : Atavistic tendencies : the culture of science in American modernity / Dana Seitler  2008 1
Atavism -- History -- 20th century : Atavistic tendencies : the culture of science in American modernity / Dana Seitler  2008 1
Atawhai. : New growth from old : the Whānau in the modern world / Joan Metge ; illustrated by Toi Te Rito Maihi  1995 1
  Ataxia -- 2 Related Subjects   2
Ataxia.   7
 

Ataxia 1, Spinocerebellar -- 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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Ataxia 2, Spinocerebellar -- 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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Ataxia 2s, Spinocerebellar -- 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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Ataxia 4, Spinocerebellar -- 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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Ataxia 4s, Spinocerebellar -- 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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Ataxia 5, Spinocerebellar -- 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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Ataxia 5s, Spinocerebellar -- 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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Ataxia 6, Spinocerebellar -- 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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Ataxia 6s, Spinocerebellar -- 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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Ataxia 7, Spinocerebellar -- 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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Ataxia 7s, Spinocerebellar -- 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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Ataxia, Appendicular -- See Ataxia


Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions
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Ataxia, Cerebellar -- See Cerebellar Ataxia


Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
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Ataxia -- Diagnosis. : Handbook of ataxia disorders / edited by Thomas Klockgether  2000 1
 

Ataxia, Dominantly-Inherited Spinocerebellar -- 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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Ataxia, Friedreich -- See Friedreich Ataxia


An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)
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