• A retrospective evaluation of coral snake envenomation in dogs and cats: 20 cases (1996-2011)
• Amyotrophic lateral sclerosis
• Amyotrophic lateral sclerosis
• Amyotrophic lateral sclerosis causes small fiber pathology
• Anesthetic and surgical management of tracheotomy in a patient with Kennedy's Disease
• Autopsy-proven case of paraneoplastic lower motor neuron disease with sensorimotor neuropathy due to Waldenstrom's macroglobulinemia
• Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?
• Blindness, weakness, and tingling
• Brown-Vialetto-Van Laere syndrome; variability in age at onset and disease progression highlighting the phenotypic overlap with Fazio-Londe disease
• Brown-Vialetto-Van Laere syndrome: clinical and neuroradiological findings of a genetically proven patient
• Case Report: Guillain-Barré Syndrome Characterized by Severe Headache Associated With Metabotropic Glutamate Receptor 5 Antibody
• Central neurodegeneration in Kennedy's disease accompanies peripheral motor dysfunction
• Chapter 15 Juvenile amyotrophic lateral sclerosis
• Childhood progressive spinal muscular atrophy with facioscapulo-humeral predominance, sensory and autonomic involvement and optic atrophy
• Chronic asymmetrical spinal muscular atrophy
• Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy
• Clinical, pathological and functional characterization of riboflavin-responsive neuropathy
• Diagnostic Clinical, Electrodiagnostic and Muscle Pathology Features of Spinal and Bulbar Muscular Atrophy
• Disentangling balance impairments in spinal and bulbar muscular atrophy
• Distal hereditary motor neuropathy type 7B with Dynactin 1 mutation
• Electrodiagnostic Evaluation of Motor Neuron Disease
• Electrodiagnostic Evaluation of Motor Neuron Disease
• Electrophysiological diagnosis of arnyotrophic lateral sclerosis
• Epidemiology, clinical spectrum of ALS and differential diagnoses
• Factors affecting the diagnostic delay in amyotrophic lateral sclerosis
• Familial bulbo-spinal muscular atrophy associated with testicular atrophy and sensory neuropathy (Kennedy-Alter-Sung syndrome). Autopsy case report of two brothers
• Familial bulbospinal neuronopathy with optic atrophy: a distinct entity
• Favorable outcome of acute porphyric neuropathy after treatment with heme arginate
• Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome
• Guillain-Barré syndrome and acute disseminated encephalomyelitis (ADEM)
• Guillain-Barré Syndrome Presenting as Painful Weakness and Edema of the Legs: A Case Report
• Hereditary motor neuron disease: the proximal, adult, sex-linked form (or Kennedy disease). Clinical and neuroendocrinologic observations
• Hereditary motor neuronopathies
• Life-threatening orthostatic hypotension in a case with bulbo-myelo-radiculo-neuropathy
• Motor neuron diseases. Present
• Nerve ultrasound detects abnormally small nerves in patients with spinal and bulbar muscular atrophy
• Neurologic course, endocrine dysfunction and triplet repeat size in spinal bulbar muscular atrophy
• Neuromyelitis Optica and Systemic Lupus Erythematosus Association – the Chicken or the Egg Dilemma: a Case Repor
• Neuromyelitis optica spectrum disorders (NMO-SD) in a Sub-Saharan Africa country: A preliminary study of sixteen Senegalese cases
• Neuropathology of paraneoplastic neuropathy with anti-disialosyl antibody
• Paraneoplastic brainstem encephalomyelitis and atypical form of chronic inflammatory demyelinating polyneuropathy in patient with testicular germinal tumor-is this an overlap syndrome? a case report
• Phenotypes in ALS--clinical features and pathology
• Prominent fatigue in spinal muscular atrophy and spinal and bulbar muscular atrophy: evidence of activity-dependent conduction block
• Respiratory insufficiency in neuronopathic and neuropathic disorders
• Reversible disruption of dynactin 1-mediated retrograde axonal transport in polyglutamine-induced motor neuron degeneration
• Sensory involvement in spinal-bulbar muscular atrophy (Kennedy's disease)
• Sensory neuropathy in X-linked recessive bulbospinal neuronopathy
• SKIN REACTION IN CHILDREN AND ADULTS WITH CENTRAL NERVOUS SYSTEM DISEASE AFTER INTRACUTANEOUS ADMINISTRATION OF MYELIN PREPARATIONS DERIVED FROM HUMAN BRAIN
• Small-fibre neuropathy related to bulbar and spinal-onset in patients with ALS
• Spinal Bulbar Muscular Atrophy -Kennedy's Disease
• The characteristic electrodiagnostic features of Kennedy's disease
• The pseudopolyneuritic form of amyotrophic lateral sclerosis (Patrikios' disease)
• TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestations
• Usefulness of electromyography in diagnostics of the neuro-muscular diseases
• X-linked recessive bulbospinal neuronopathy--Kennedy's syndrome