Results 81 to 90 of about 38,305 (257)

Paroxysmal slow wave events as a diagnostic biomarker for epilepsy: Lessons from rural Zambia

open access: yesEpilepsia, EarlyView.
Abstract Objective Epilepsy affects more than 50 million people globally, with low‐ and middle‐income countries (LMICs) bearing the greatest burden due to limited medical resources and stigma. Electroencephalography (EEG) is a cost‐effective diagnostic tool, but its interpretation often requires unavailable expertise in rural areas. There is a pressing
Andrew Malunga   +21 more
wiley   +1 more source

Migraine and patent foramen ovale: correlation, coexistence, dependence. A narrative review

open access: yesHeadache: The Journal of Head and Face Pain, EarlyView.
Plain Language Summary This review looked at what scientists know about the connection between migraine and a small heart opening called a patent foramen ovale (PFO). It showed that people with migraine, especially with aura, often have PFO, but it is not certain whether closing this heart opening helps prevent strokes in these patients.
Olga Grodzka   +5 more
wiley   +1 more source

Measuring Direct Oral Anticoagulant (DOAC) Levels: Applications, Limitations, and Future Directions

open access: yesInternational Journal of Laboratory Hematology, EarlyView.
ABSTRACT Introduction There are important challenges with the measurement and interpretation of direct oral anticoagulant (DOAC) anticoagulant effect including a lack of therapeutic ranges, inaccuracy of routinely available coagulation assays, lack of established thresholds for clinically significant effect, and uncertainty about how to apply the ...
Siraj Mithoowani   +2 more
wiley   +1 more source

Selective contralesional constructional hemi‐apraxia after unilateral brain damage: Which relationship with unilateral spatial neglect?

open access: yesJournal of Neuropsychology, EarlyView.
Abstract We describe a peculiar contralesional drawing disorder in three patients affected by focal brain lesions, who did not show signs of unilateral neglect at standard clinical assessment, including the star cancellation test. This picture, that could be termed selective constructional hemi‐apraxia (CHA), could follow both right and left‐hemisphere
Francesco Panico   +3 more
wiley   +1 more source

Endovascular Treatment of Brain Arteriovenous Malformations in Siriraj Hospital

open access: yesSiriraj Medical Journal, 2020
Objective : To present our experience on endovascular embolization by using N-butyl cyanoacrylate and to demonstrate that this is an effective method in the treatment of brain arteriovenous malformations.
Anchalee Churojana   +4 more
doaj  

Cerebral Arteriovenous Malformations

open access: yesPediatric Neurology Briefs, 1994
A retrospective analysis of 62 children with cerebral arteriovenous malformations (AVM) seen over 17 years is reported from Hospital B, Lille, France.
J Gordon Millichap
doaj   +1 more source

Arteriovenous Malformation

open access: yesPediatric Neurology Briefs, 1987
Three children, ages 5 to 9 years, with A-V malformations that ruptured after trivial head trauma, are reported from the Departments of Neurosurgery, University Medical School and Red Cross Hospital, Kumamoto City, Japan.
openaire   +3 more sources

Lipoma of the Buccal Fat Pad: Systematic Review and Report of a Case

open access: yesOral Surgery, EarlyView.
ABSTRACT Introduction Lipomas in the oral cavity are uncommon, defined by the abnormal proliferation of mature adipocytes. When they arise from the buccal fat pad (BFP), these lipomas frequently impact both the cosmetic appearance and the functional aspects of the face. Objectives The aim of the present review is to investigate the incidence of the BFP
Silvia D'Agostino   +2 more
wiley   +1 more source

Visualizing Genetics: An Investigation of Dermoscopy as a Tool for Genetic Variant Prediction in Capillary Malformations

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Background/Objectives Capillary malformations (CMs) are congenital malformations of capillaries typically visible as blanchable, pink to brown patches on the skin and/or mucosa. The genetic cause of CMs guides diagnosis, treatment, and recurrence counseling.
Aretha On   +6 more
wiley   +1 more source

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