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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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A 42-year-old man with unilateral leg weakness
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Young Adult with Dysphagia and Severe Weight Loss
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
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Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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Spinal Muscular Atrophy A Timely Review
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Spinal Muscular Atrophy
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Amyotrophic Lateral Sclerosis
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Familial Amyotrophic Lateral Sclerosis
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Molecular Basis of the Neurodegenerative Disorders
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Distal Hereditary Upper Limb Muscular Atrophy
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Hereditary Form of Parkinsonism-Dementia
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Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
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Neurogenic Muscle Hypertrophy
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Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
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Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Location of the Gene for X-Linked Spinal Muscular Atrophy
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Lathyrism:Evidence for Role of the Neuroexcitatory Aminoacid BOAA
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Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
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Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
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Conjugal Amyotrophic Lateral Sclerosis
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Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
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Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
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Progressive Pontobulbar Palsy With Deafness
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