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Motor neuron disease

  • Clinically Undetected Motor Neuron Disease in Pathologically Proven Frontotemporal Lobar Degeneration with Motor Neuron Disease

    Clinically Undetected Motor Neuron Disease in Pathologically Proven Frontotemporal Lobar Degeneration with Motor Neuron Disease

  • Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia

    Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia

  • ALS and Other Motor Neuron Diseases Can Represent Diagnostic Challenges

    ALS and Other Motor Neuron Diseases Can Represent Diagnostic Challenges

  • Motor Neuron Disease and the Elderly

    Motor Neuron Disease and the Elderly

  • Exacerbation of Motor Neuron Disease by Chronic Stimulation of Innate Immunity in a Mouse Model of Amyotrophic Lateral Sclerosis

    Exacerbation of Motor Neuron Disease by Chronic Stimulation of Innate Immunity in a Mouse Model of Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease Motor Neuron Disease

    Motor Neuron Disease Motor Neuron Disease

  • Amyotrophic Lateral Sclerosis (ALS)

    Amyotrophic Lateral Sclerosis (ALS)

  • Dissociated Leg Muscle Atrophy in Amyotrophic Lateral

    Dissociated Leg Muscle Atrophy in Amyotrophic Lateral

  • Studies of Cellular Hypersensitivityto Ionising Radiation in Friedreich's

    Studies of Cellular Hypersensitivityto Ionising Radiation in Friedreich's

  • Unilateral Progressive Muscular Atrophy with Fast Symptoms

    Unilateral Progressive Muscular Atrophy with Fast Symptoms

  • Motor Neuron Disease

    Motor Neuron Disease

  • Review of 48 Cases of Motor Neuron Disease Seen at Groote Schuur Hospital: a Pilot Study

    Review of 48 Cases of Motor Neuron Disease Seen at Groote Schuur Hospital: a Pilot Study

  • Animal Models for Motor Neuron Disease

    Animal Models for Motor Neuron Disease

  • Noncoding Repeat Expansions for ALS in Japan Are Associated with the ATXN8OS Gene

    Noncoding Repeat Expansions for ALS in Japan Are Associated with the ATXN8OS Gene

  • AMYOTROPHIC LATERAL SCLEROSIS (ALS Or Lou Gehrig’S Disease)

    AMYOTROPHIC LATERAL SCLEROSIS (ALS Or Lou Gehrig’S Disease)

  • Motor Neuron Disease-Associated Loss of Nuclear TDP-43 Is

    Motor Neuron Disease-Associated Loss of Nuclear TDP-43 Is

  • Motor Neuron Disease Andpolio in Scotland

    Motor Neuron Disease Andpolio in Scotland

  • Psychological Interventions for People with Huntington's Disease

    Psychological Interventions for People with Huntington's Disease

Top View
  • Association of Long ATXN2 CAG Repeat Sizes with Increased Risk of Amyotrophic Lateral Sclerosis
  • From First Symptoms to Diagnosis of Amyotrophic Lateral
  • Electrodiagnosis of Motor Neuron Disease
  • Cognitive and Behavioral Manifestations in ALS: Beyond Motor System Involvement
  • Differentiating Lower Motor Neuron Syndromes
  • ALS, MS and MD | Fact Sheet ALS, MS, and MD: How Do They Differ? Often, the Public Confuses Multiple Sclerosis, Muscular Dystrophy, and Amyotrophic Lateral Sclerosis
  • Defining Post-Polio Problems
  • The Relationship Between Alzheimer's Disease, Parkinson's Disease and Motor Neuron Disease
  • Motor Neurone Disease: Clinical Features, Diagnosis, Diagnostic Pitfalls and Prognostic Markers Sathasivam S
  • Mimickers of Cervical Spondylotic Myelopathy
  • Motor Neuron Disease: Biomarker Development for an Expanding Cerebral Syndrome
  • 18 EDX Studies in ALS and Other Motor Neuron Disorders.Pdf
  • Ncr130038.Pdf
  • The Impact of Robotic Rehabilitation on the Motor System in Neurological Diseases
  • The Environment in Childhood and Risk of Motor Neuron Disease
  • Clinical Reasoning: a 26-Year-Old Man with Right Hand and Arm Weakness
  • Motor Neuron Disease
  • Motor Neurone Disease: a Practical Update on Diagnosis and Management


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