• A case of X-linked bulbospinal muscular atrophy with bilateral abductor vocal cord paralysis
• A case of X-linked recessive bulbospinal muscular atrophy with demyelinating neuropathy and hypertrophy of the calves
• A familial case of Kennedy's X-linked bulbospinal amyotrophy
• A family study of the association between X-linked bulbospinal muscular atrophy (Kennedy-Alter-Sung type) and color blindness protan
• A sporadic case of bulbospinal muscular atrophy of late onset
• A weak man... X chromosome associated progressive bulbospinal neuropathy (or bulbospinal amyotrophy) or Kennedy syndrome
• Central motor and sensory conduction in X-linked recessive bulbospinal neuronopathy
• Chromosome X-linked recessive bulbospinal neuronopathy (Kennedy's syndrome)
• Chronic X-linked recessive bulbospinal amyotrophy (Kennedy-Stefanis type). Apropos of a case
• Clinical and electrodiagnostic features of X-linked recessive bulbospinal neuronopathy
• Decrease in androgen binding and effect of androgen treatment in a case of X-linked bulbospinal neuronopathy
• Decremental responses to repetitive nerve stimulation in x-linked bulbospinal muscular atrophy
• Distinguishing clinical and electrodiagnostic features of X-linked bulbospinal neuronopathy
• DNA diagnosis of X-linked recessive bulbospinal muscular atrophy by androgen receptor gene mutations
• DNA-diagnosis of bulbospinal muscular atrophy (Kennedy's disease)
• Dysphagia in X-linked bulbospinal muscular atrophy (Kennedy disease)
• Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women
• Fatigue and abnormal neuromuscular transmission in Kennedy's disease
• General Anesthesia With Successful Immediate Post-operative Extubation for Sarcoma Excision in a 61-Year-Old Male With Kennedy's Disease
• Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapy
• Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
• Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene
• Loss of spinal anterior horn cells in X-linked recessive bulbospinal muscular atrophy--a morphometric study of lower motoneuron loss
• Maximal and minimal motor conduction velocity in amyotrophic lateral sclerosis and X-linked bulbospinal muscular atrophy measured by Harayama's collision method
• Mitochondrial implications in bulbospinal muscular atrophy (Kennedy disease)
• Molecular genetics and clinical aspects of inherited disorders of nerve and muscle
• Morphometric quantification of spinal and cranial nerve roots in amyotrophic lateral sclerosis and adult onset X-linked recessive bulbo-spinal muscular atrophy (author's transl)
• Onset Manifestations of Spinal and Bulbar Muscular Atrophy (Kennedy's Disease)
• Overcoming neurological diseases-breakthrough for new era
• Perspectives of Kennedy's disease
• Quinine-responsive muscle cramps in X-linked bulbospinal muscular atrophy Kennedy
• Random X chromosome methylation patterns in the carriers with clinical phenotypic expressions of X-linked recessive bulbospinal neuronopathy
• Risk estimates for developing motor neurone disease in first-degree relatives
• Sandhoff disease mimicking adult-onset bulbospinal neuronopathy
• Sensory ataxia as the initial clinical symptom in X-linked recessive bulbospinal neuronopathy
• Sensory nerve involvement in X-linked bulbospinal amyotrophy (Kennedy syndrome). Contributions of electrophysiologic and histologic data
• Sensory neuropathy in X-linked recessive bulbospinal neuronopathy
• Somatosensory evoked potentials in X-linked recessive bulbospinal neuronopathy: a case demonstration
• Spinal and cranial motor nerve roots in amyotrophic lateral sclerosis and X-linked recessive bulbospinal muscular atrophy: morphometric and teased-fiber study
• Testosterone therapy and the pathogenesis of Kennedy's disease (X-linked bulbospinal muscular atrophy)
• Tremor in X-linked recessive spinal and bulbar muscular atrophy (Kennedy's disease)
• Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy
• Very late onset X-linked recessive bulbospinal neuronopathy: mild clinical features and a mild increase in the size of tandem CAG repeat in androgen receptor gene
• X-chromosomal bulbospinal muscular atrophy (Kennedy syndrome)
• X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy
• X-linked bulbo-spinal neuronopathy of late onset: sporadic case
• X-linked bulbo-spinal neuronopathy: a family study of three patients
• X-linked bulbo-spinal neuronopathy. Kennedy's syndrome
• X-linked bulbospinal muscular atrophy (Kennedy's syndrome): a report of three cases
• X-linked bulbospinal neuronopathy: Kennedy disease
• X-linked recessive bulbospinal muscular atrophy (Kennedy's disease). A family study
• X-linked recessive bulbospinal neuronopathy
• X-linked recessive bulbospinal neuronopathy (SBMA)
• X-linked recessive bulbospinal neuronopathy--Kennedy's syndrome
• X-linked recessive bulbospinal neuronopathy: a report of ten cases
• X-linked recessive bulbospinal neuronopathy: clinical phenotypes and CAG repeat size in androgen receptor gene
• X-linked recessive bulbospinal neuropathy (Kennedy syndrome)
• X-linked spinal muscular atrophy (Kennedy's syndrome). A kindred with hypobetalipoproteinemia