Results 1 to 10 of about 29,127 (251)

Metabolic stroke-like episode in a child with FARS2 mutation and SARS-CoV-2 positive cerebrospinal fluid [PDF]

open access: yesMolecular Genetics and Metabolism Reports, 2021
The novel SARS-CoV-2 has infected over 48 million persons around the world. Children have been spared with regards to symptoms and sequelae of this highly infectious virus and in those with neurologic issues, the virus has not been present in the ...
Kelly T. Powers, Jonathan D. Santoro
doaj   +4 more sources

Perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode: A case report [PDF]

open access: yesCerebral Circulation - Cognition and Behavior, 2022
Neuronal intranuclear inclusion disease (NIID) is a slowly progressive neurodegenerative disease. Some patients with NIID occasionally present with acute symptoms. However, its mechanism remains unclear. We report a patient with NIID who presented with a
Fumiya Kutsuna   +11 more
doaj   +4 more sources

Cerebral amyloid angiopathy-related inflammation presenting with a stroke-like episode [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2023
Cerebral amyloid angiopathy (CAA) is characterised by B-amyloid deposition in the walls of small to medium sized arteries of the cerebral cortex and the leptomeninges.
Ana Rita Gaspar   +3 more
doaj   +2 more sources

Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2019
Background Maternally inherited diabetes and deafness, and mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes are examples of mitochondrial diseases that are relatively common in the adult population. Mitochondrial myopathy,
Mai Fukuda, Yoshiro Nagao
doaj   +2 more sources

New Trigger for Stroke-like Episode in Sturge–Weber Syndrome: A Case Report [PDF]

open access: yesChildren
Background. Sturge–Weber syndrome (SWS) is a rare non-hereditary neurovascular disorder characterized by capillary–venous malformations on the face, ocular vascular anomalies, and leptomeningeal capillary–venous malformations.
Emiliano Altavilla   +9 more
doaj   +2 more sources

Acute management of a stroke-like episode in MELAS syndrome: What should we know? [PDF]

open access: yeseNeurologicalSci, 2020
Tirso González-Pinto González   +6 more
doaj   +2 more sources

Recurrent Miscarriages and Postpartum Heart Failure Can Be Phenotypic Manifestations of the m.3243A>G Variant [PDF]

open access: yesClinical Case Reports
Female carriers of the MT‐TL1 variant m.3243A>G may manifest not only phenotypically with diabetes, renal insufficiency, hearing loss, and cardiomyopathy but also with recurrent miscarriages.
Sounira Mehri, Josef Finsterer
doaj   +2 more sources

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