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Amyloplast -- See Plastids


Self-replicating cytoplasmic organelles of plant and algal cells that contain pigments and may synthesize and accumulate various substances. PLASTID GENOMES are used in phylogenetic studies
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Amyloplasts -- See Plastids


Self-replicating cytoplasmic organelles of plant and algal cells that contain pigments and may synthesize and accumulate various substances. PLASTID GENOMES are used in phylogenetic studies
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  Amylum -- 2 Related Subjects   2
  Amyotonia Congenita -- 2 Related Subjects   2
Amyotrophic lateral sclerosis.   46
Amyotrophic lateral sclerosis -- Australia. : Morbidity of Vietnam veterans : multiple sclerosis and motor neurone disease in Vietnam veterans : supplementary report no. 3  2001 1
Amyotrophic lateral sclerosis -- Biography.   3
Amyotrophic lateral sclerosis -- Case studies : Sunday Morning. Against the Odds / producer, George Osterkamp  2012 1
Amyotrophic lateral sclerosis -- Diagnosis : 60 minutes. Saving Stephen Heywood / produced by Rob Wallace  2000 1
Amyotrophic lateral sclerosis -- Fiction. : Every breath / Nicholas Sparks  2018 1
Amyotrophic lateral sclerosis -- Government policy : Public policy in ALS/MND care : an international perspective / Robert H. Blank, Jerome E. Kurent, David Oliver, editors  2021 1
Amyotrophic lateral sclerosis -- Guam. : The island of the colorblind : and, Cycad island / by Oliver Sacks  1997 1
 

Amyotrophic Lateral Sclerosis, Guam Form -- See Amyotrophic Lateral Sclerosis


A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
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Amyotrophic lateral sclerosis -- Handbooks, manuals, etc. : The motor neurone disease handbook / edited by Matthew Kiernan  2007 1
Amyotrophic lateral sclerosis -- Nursing. : Aspects of care for staff of residential care facilities : Motor neurone disease  2006 1
 

Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1 -- See Amyotrophic Lateral Sclerosis


A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
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Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam -- See Amyotrophic Lateral Sclerosis


A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
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Amyotrophic lateral sclerosis -- Patients   20
Amyotrophic lateral sclerosis -- Patients -- Biography   8
Amyotrophic lateral sclerosis -- Patients -- Care : Getting up : the Tempt One story / TEG presents in association with Not Impossible Foundation ; produced by Jon Barlow ; directed by Caskey  2012 1
Amyotrophic lateral sclerosis -- Patients -- Family relationships.   3
Amyotrophic lateral sclerosis -- Patients -- Family relationships -- Great Britain : Filming my father : in life and death / filmed by Fraser Isaac ; director and executive producer, Liz Tucker ; Verve Productions  2014 1
Amyotrophic lateral sclerosis -- Patients -- Fiction. : Every breath / Nicholas Sparks  2018 1
Amyotrophic lateral sclerosis -- Patients -- Great Britain -- Biography   2
Amyotrophic lateral sclerosis -- Patients -- Great Britain -- Biography -- Comic books, strips, etc : Hawking / written by Jim Ottaviani ; art by Leland Myrick ; coloring by Aaron Polk  2019 1
Amyotrophic lateral sclerosis -- Patients -- Ireland -- Biography : It's not yet dark / [FilmRise] ; Newgrange Pictures [and Kennedy Films] presents ; [in association with Bord Scannán na hÉireann / the Irish Film Board ; in association with TV3 and [3 others]] ; produced by Lesley McKimm and Kathryn Kennedy ; directed by Frankie Fenton  2016 1
Amyotrophic lateral sclerosis -- Patients -- United States -- Biography   3
Amyotrophic lateral sclerosis -- Patients -- United States -- ?́ƠBiography : Tuesdays with Morrie : an old man, a young man, and life's greatest lesson / Mitch Albom  1998 1
Amyotrophic lateral sclerosis -- Periodicals   3
Amyotrophic Lateral Sclerosis -- physiopathology. : Definitions, clinical features, and morphology / editorial board, D.B. Calne ... [and others]  1993 1
Amyotrophic lateral sclerosis -- Popular works   2
Amyotrophic lateral sclerosis -- Psychological aspects.   6
Amyotrophic lateral sclerosis -- Research   4
Amyotrophic Lateral Sclerosis -- therapy.   2
Amyotrophic lateral sclerosis -- Treatment : Sunday morning. Close to home / producer, George Osterkamp  2005 1
Amyotrophic lateral sclerosis -- Treatment -- Government policy : Public policy in ALS/MND care : an international perspective / Robert H. Blank, Jerome E. Kurent, David Oliver, editors  2021 1
 

Amyotrophic Lateral Sclerosis With Dementia -- See Amyotrophic Lateral Sclerosis


A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
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Amyotrophies, Diabetic -- See Diabetic Neuropathies


Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325)
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Amyotrophy -- See Muscular atrophy


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Amyotrophy, Diabetic -- See Diabetic Neuropathies


Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325)
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Amyotrophy, Thenar, Of Carpal Origin -- See Carpal Tunnel Syndrome


Entrapment of the MEDIAN NERVE in the carpal tunnel, which is formed by the flexor retinaculum and the CARPAL BONES. This syndrome may be associated with repetitive occupational trauma (CUMULATIVE TRAUMA DISORDERS); wrist injuries; AMYLOID NEUROPATHIES; rheumatoid arthritis (see ARTHRITIS, RHEUMATOID); ACROMEGALY; PREGNANCY; and other conditions. Symptoms include burning pain and paresthesias involving the ventral surface of the hand and fingers which may radiate proximally. Impairment of sensation in the distribution of the median nerve and thenar muscle atrophy may occur. (Joynt, Clinical Neurology, 1995, Ch51, p45)
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Amyotropic lateral sclerosis   2
Amyotropic lateral sclerosis -- Patients -- Australia : Negotiating life choices : living with motor neurone disease / Susan Jane King  2005 1
Amyris, Inc : Amyris, Inc : make good, no compromise / J. Miguel Villas-Boas, Juan Guillermo Norero  2019 1
Amyton (S. A.) -- History : Plain of contrast : a history of Willowie, Amyton, Booleroo Whim / compiled by the District Centenary Book Committee ; edited by Liz Blieschke  1975 1
Amyton (S. Aust.) : Plain of contrast : a history of Willowie, Amyton, Booleroo Whim / compiled by the District Centenary Book Committee ; edited by Liz Blieschke  1975 1
Amyton (S. Aust.) -- History : Plain of contrast : a history of Willowie, Amyton, Booleroo Whim / compiled by the District Centenary Book Committee ; edited by Liz Blieschke  1975 1
 

Amytornis -- See Grasswrens


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An-225 (Transport plane) : Cutting edge. Episode 8 / produced by Evan Clark  2003 1
Great Britain. Parliament. An act declaring the rights and liberties of the subject and settling the succession of the crown, 1688 : The Declaration of Rights, 1689 / Lois G. Schwoerer  1981 1
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