Frontiers in Neurology, 2018 IgLON5-associated encephalitis is a syndrome with different clinical presentations consisting of sleep dysfunction, bulbar dysfunction, chorea, and progressive supranuclear palsy-like symptoms whereas dysautonomy and cognitive decline usually appear in ...
Massimiliano Montagna +8 more
doaj +1 more source
陆军军医大学学报, 2023 Objective To investigate the clinical and imaging features of the characteristic "heart appearance" isolated cerebral infarction involving bilateral pons-medulla oblongata.
DIAO Shengpeng +4 more
doaj +1 more source
Accuracy of routinely-collected healthcare data for identifying motor neurone disease cases: a systematic review [PDF]
, 2017 Background Motor neurone disease (MND) is a rare neurodegenerative condition, with poorly understood aetiology. Large, population-based, prospective cohorts will enable powerful studies of the determinants of MND, provided identification of disease cases
Horrocks, Sophie +5 more
core +1 more source
Guillain–Barré syndrome with unilateral peripheral facial and bulbar palsy in a child: A case report
SAGE Open Medical Case Reports, 2019 Guillain–Barré syndrome is characterized by progressive motor weakness, sensory changes, dysautonomia, and areflexia. Cranial nerve palsies are frequent in Guillain–Barré syndrome.
Kamal Sharma +4 more
doaj +1 more source
Tremor in motor neuron disease may be central rather than peripheral in origin [PDF]
, 2018 BACKGROUND AND PURPOSE: Motor neuron disease (MND) refers to a spectrum of degenerative diseases affecting motor neurons. Recent clinical and post-mortem observations have revealed considerable variability in the phenotype.
Balint, B +9 more
core +2 more sources
Fatal subarachnoid hemorrhage following ischemia in vertebrobasilar dolichoectasia. [PDF]
, 2016 Vertebrobasilar dolichoectasia (VBD) is a chronic disorder with various cerebrovascular and compressive manifestations, involving subarachnoid hemorrhage (SAH).
Caso, V. +10 more
core +7 more sources
Clinical Features of Isolated Bulbar Palsy of Amyotrophic Lateral Sclerosis in Chinese Population
Chinese Medical Journal, 2017 Background: Progressive bulbar palsy (PBP) is a classic phenotype of bulbar onset amyotrophic lateral sclerosis (ALS) with more rapid progression and worse prognosis.
Hua-Gang Zhang +4 more
doaj +1 more source
Progress and challenges in directing the differentiation of human iPSCs into spinal motor neurons
Frontiers in Cell and Developmental Biology, 2023 Motor neuron (MN) diseases, including amyotrophic lateral sclerosis, progressive bulbar palsy, primary lateral sclerosis and spinal muscular atrophy, cause progressive paralysis and, in many cases, death.
Cristina Marisol Castillo Bautista +2 more
doaj +1 more source
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family [PDF]
, 2018 Riboflavin transporter deficiency (formerly known as Brown-Vialetto-Van Laere [BVVL] or Fazio-Londe syndrome) is a neurodegenerative disorder characterized by progressive bulbar palsy with sensorineural deafness or bulbar hereditary neuropathy.1 It is ...
Bras, J +3 more
core +1 more source
FACTORS AFFECTING THE DIAGNOSTIC DELAY IN AMYOTROPHIC LATERAL SCLEROSIS [PDF]
, 2012 Background: Although amyotrophic lateral sclerosis (ALS) is a relentlessly progressive disorder, early diagnosis allows a prompt start with the specific drug riluzole and an accurate palliative care planning.
CELLURA, Eleonora +3 more
core +1 more source