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Amyloidosis -- Congresses   2
Amyloidosis -- diagnosis.   5
Amyloidosis -- etiology. : Protein misfolding diseases : current and emerging principles and therapies / edited by Marina Ramirez-Alvarado, Jeffery W. Kelly, Christopher M. Dobson  2010 1
Amyloidosis -- genetics : Water and biomolecules : physical chemistry of life phenomena / Kunihiro Kuwajima [and others] (editors)  2009 1
Amyloidosis -- pathology   2
Amyloidosis -- Patients -- Women : Navigating the inequitable U.S. healthcare system in search of critical care / Kellina Craig-Henderson  2024 1
Amyloidosis -- Periodicals : Amyloid (Online)  1994- 1
Amyloidosis -- physiopathology   2
Amyloidosis -- therapy   4
Amyloidosis -- Treatment   2
 

Amylomaize Starch -- See Starch


Any of a group of polysaccharides of the general formula (C6-H10-O5)n, composed of a long-chain polymer of glucose in the form of amylose and amylopectin. It is the chief storage form of energy reserve (carbohydrates) in plants
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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.   2
Amyotrophic lateral sclerosis -- Case studies : Sunday Morning. Against the Odds / producer, George Osterkamp  2012 1
Amyotrophic lateral sclerosis -- Complications : What you need to know about ALS / Harry LeVine III  2019 1
Amyotrophic lateral sclerosis -- Diagnosis   3
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   21
Amyotrophic lateral sclerosis -- Patients -- Biography   7
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.   2
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   5
Amyotrophic Lateral Sclerosis -- therapy.   2
Amyotrophic lateral sclerosis -- Treatment   2
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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