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2,383 Possible Causes for Amyotrophic Lateral Sclerosis, DECR Enzyme Activity Decreased

  • Alzheimer Disease

    Aluminum has been associated with neurodegenerative diseases such as Alzheimer's disease (AD), amyotrophic lateral sclerosis, and dialysis encephalopathy.[] Abstract Alzheimer disease (AD), Frontotemporal lobar degeneration (FTD), Amyotrophic lateral sclerosis (ALS) and Parkinson disease (PD) have a certain degree of clinical,[]

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  • Cervical Spondylosis

    INTRODUCTION: Cervical spondylosis (CS) is a common disease in adults and may coexist with amyotrophic lateral sclerosis (ALS).[] […] and amyotrophic lateral sclerosis.[] Amyotrophic lateral sclerosis can resemble cervical spondylotic amyotrophy and it is possible for patients to present with both, thus posing a diagnostic problem due to both[]

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  • Parkinson's Disease

    Amyotrophic lateral sclerosis (ALS), frontotemporal degeneration and Parkinson's disease may be different expressions of the same neurodegenerative disease.[] lateral sclerosis.[] (MS), neuromyelitis optica (NMO) and amyotrophic lateral sclerosis (ALS).[]

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  • Epilepsy

    .: IgM deposits at nodes of Ranvier in a patient with amyotrophic lateral sclerosis, anti-GM1 antibodies, and multifocal motor conduction block.[] Mohamed, Shashirekha Markandaiah, Silvia Bonanno, Piera Pasinelli and Davide Trotti, Blood–Brain Barrier Driven Pharmacoresistance in Amyotrophic Lateral Sclerosis and Challenges[]

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  • Amyotrophic Lateral Sclerosis

    Frontotemporal white matter changes in amyotrophic lateral sclerosis.[] What is amyotrophic lateral sclerosis (ALS)?[] Lithium delays progression of amyotrophic lateral sclerosis.[]

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  • Primary Lateral Sclerosis

    Both amyotrophic lateral sclerosis (ALS) and primary lateral sclerosis (PLS) fall under the umbrella of motor neuron diseases.[] Primary lateral sclerosis differs from amyotrophic lateral sclerosis by its lack of lower motor neuron signs and long survival.[] Here we report a novel pedigree highlighting an intrafamilial occurrence of PLS and amyotrophic lateral sclerosis (ALS) cases.[]

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  • Paraneoplastic Syndrome

    Paraneoplastic primary lateral sclerosis and amyotrophic lateral sclerosis.[] lateral sclerosis.[] Zachary Simmons, Amyotrophic Lateral Sclerosis–Like Syndromes Associated with Malignancy, Neurobiology of Disease, 10.1016/B978-012088592-3/50047-5, (513-519), (2007).[]

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  • Shy Drager Syndrome

    lateral sclerosis (5 cases) and an age-matched control group (4 cases).[] lateral sclerosis (ALS), and five patients with nonneurologic symptoms.[] lateral sclerosis, a cerebellar system degeneration and a loss of approximately 75% of sympathetic preganglionic neurons.[]

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  • Patulous Eustachian Tube

    We report a 60-year-old case diagnosed as the amyotrophic lateral sclerosis with patulous eustachian tube (ET).[] We report a 64-year-old female with predominantly bulbar amyotrophic lateral sclerosis who experienced 'roaring' in her ears.[] To our knowledge, this is the first case report of the amyotrophic lateral sclerosis complicating patulous ET in the literature, demonstrating the movement of the tympanic[]

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  • Syringomyelia

    Differential Diagnosis is retroolivar syndrome, hematomielia, amyotrophic lateral sclerosis, chronic anterior poliomyelitis, leprosy, disease Morvan, intramedullary tumors[] Amyotrophic lateral sclerosis. There is no sensory abnormality, and there are generalized increased tendon reflexes in ALS. 5. Cervical spondylosis.[] Syphilitic amyotrophy resembles amyotrophic lateral sclerosis and is caused by progressive loss of anterior horn cells secondary to ischemia due to an arteritis involving[]

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