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2,857 Possible Causes for Amyotrophic Lateral Sclerosis

  • 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,[]

  • 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[]

  • 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).[]

  • 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[]

  • Progressive Muscular Atrophy

    Trojanowski, Motor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy, Acta Neuropathologica, 121, 4, (509), (2011). F.[] Abstract Serum and CSF from 48 patients with amyotrophic lateral sclerosis and six patients with late-onset postpoliomyelitis progressive muscular atrophy were investigated[] Abstract Twelve cases of adult-onset progressive muscular atrophy variant of amyotrophic lateral sclerosis (PMA/ALS) were studied in a small rural population of 1500 in the[]

  • Amyotrophic Lateral Sclerosis

    Medication in the last days of life for motor neuron disease/amyotrophic lateral sclerosis. Amyotroph. Lateral Scler. 11, 562–564 (2010). 35.[] Amyotrophic lateral sclerosis (ALS) is one of the most common forms of motor neuron diseases.[] Familial adult motor neuron disease: amyotrophic lateral sclerosis.[]

  • 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.[] Abstract Among the motor neuron diseases, three share the clinical features of prominent upper motor neuron signs--amyotrophic lateral sclerosis (ALS), primary lateral sclerosis[]

  • 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).[]

  • Progressive Bulbar Palsy

    Motor Neuron Disease (or ‘amyotrophic lateral sclerosis’, ALS). ‘’Brain Damage, Brain Repair.’’[] Amyotrophic lateral sclerosis (Lou Gehrig disease) is the most common form of motor neuron disease.[] Eventually this condition may become indistinguishable from amyotrophic lateral sclerosis.[]

  • Shy Drager Syndrome

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

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