Disease: Hereditary sensory and autonomic neuropathy type 3 (Familial Dysautonomia)
- Assessing microcirculation in familial dysautonomia by laser Doppler flowmeter
- Bone mineral density and metabolism in familial dysautonomia
- Brainstem reflexes in patients with familial dysautonomia
- Cardiac-locked bursts of muscle sympathetic nerve activity are absent in familial dysautonomia
- Chemoreflex failure and sleep-disordered breathing in familial dysautonomia: Implications for sudden death during sleep
- Congenital hypoventilation syndromes
- Correlation between clinical, electromyographic and dysautonomic evolution of familial amyloidotic polyneuropathy of the Portuguese type
- Defects in tongue papillae and taste sensation indicate a problem with neurotrophic support in various neurological diseases
- Disturbances in affective touch in hereditary sensory & autonomic neuropathy type III
- Disturbances in affective touch in hereditary sensory & autonomic neuropathy type III
- Familial dysautonomia
- Hereditary sensory and autonomic neuropathy type 3 in non-Jewish child
- Herpes simplex virus-1 and varicella virus infections in familial dysautonomia patients
- Impaired sensorimotor control of the hand in congenital absence of functional muscle spindles
- Increasing cutaneous afferent feedback improves proprioceptive accuracy at the knee in patients with sensory ataxia
- Long-term survival in Stuve-Wiedemann syndrome: a neuro-myo-skeletal disorder with manifestations of dysautonomia
- Modeling pain in vitro using nociceptor neurons reprogrammed from fibroblasts
- Onabotulinum toxin A for the treatment of sialorrhea in familial dysautonomia
- Pain insensitivity syndrome misinterpreted as inflicted burns
- Relationship between proprioception at the knee joint and gait ataxia in HSAN III
- Riley-Day Syndrome in a Hispanic Infant of Non-Jewish Ashkenazi Descent
- The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene
- The impact of autonomic nervous system dysfunction on breathing during sleep
- Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia
- Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomia