Analysis of characteristics and prognostic impact of phenotypes in hereditary ATTR Free

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Early and late outcome of treated patients referred for syncope to emergency department: the EGSYS 2 follow-up study Get access

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Ictal bradycardia in partial epileptic seizures: Autonomic investigation in three cases and literature review Get access

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Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels Get access

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`Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation Get access

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Progressive disruption of the circadian rhythm of melatonin in fatal familial insomnia Get access

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Fatal familial insomnia and the widening spectrum of prion diseases Get access

Clinical, Autonomic and Therapeutic Observations in Two Siblings With Postural Hypotension and Sympathetic Failure due to an Inability to Synthesize Noradrenaline From Dopamine Because of a Deficiency of Dopamine Beta Hydroxylase Get access

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