Auflistung Nach Schlagwort "dysarthria"
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The frequency of central nervous system complications in the Cypriot cohort of ATTRV30M neuropathy transplanted patients
(2020)Background: Hereditary transthyretin amyloidosis (ATTR) is a hereditary, sensorimotor and autonomic neuropathy caused by deposits of mutated transthyretin (TTR). The commonest TTR mutation is V30M (ATTRV30M) with patients ... -
Hereditary cerebral amyloid angiopathy mimicking CADASIL syndrome
(2021)Background: Small vessel disease (SVD), and most specifically hereditary forms like CADASIL and cerebral amyloid angiopathy (hCAA), are conditions of increasing clinical importance. We report a rare case of hCAA in a Greek ... -
Posterior reversible encephalopathy in a GT1a positive oculopharyngeal variant of Guillain-Barré syndrome: A case-report and review of the literature
(2020)Guillain-Barre syndrome (GBS) is the most common cause of acute flaccid paralysis and its incidence increases with age, although all age groups can be affected. The cranial subtypes of GBS account for approximately 5% of ... -
Primary Sjögren’s syndrome (pSS)-related cerebellar ataxia: a systematic review and meta-analysis
(2022)Background: Primary Sjögren’s syndrome (pSS) is a chronic autoimmune disorder characterized by lymphocytic infiltrates of the exocrine glands, particularly the salivary and lacrimal glands, resulting in oral and ocular ...