Results 61 to 70 of about 1,617,655 (156)
Frontiers in Neurology, 2020 Moyamoya disease (MMD) is a chronic cerebrovascular disease that frequently results in intracranial ischemia or hemorrhage. Its concurrence with varying ophthalmic findings is relatively rare yet may lead to irreversible blindness.
Yue-ye Wang +6 more
doaj +1 more source
Movement Disorders Clinical Practice, Volume 12, Issue 8, Page 1066-1074, August 2025.Abstract Background Restless Legs Syndrome (RLS) is a neurological disorder reported to be associated with impulsivity and impairments in interoception and emotional regulation. However, limited research has explored the combined influence of RLS severity, psychological factors, and chronotype on impulsive decision‐making and risk‐taking behavior in ...
Giacomo Carollo +5 more
wiley +1 more source
Clinical &Experimental Ophthalmology, Volume 53, Issue 6, Page 682-697, August 2025.ABSTRACT Optical coherence tomography angiography is a burgeoning imaging modality in Ophthalmology. In this review, we outline the breadth of potential utility for optical coherence tomography angiography for diagnosis and prognostication in neuro‐ophthalmology.
Marzieh Tahmasebi Sarvestani +2 more
wiley +1 more source
Molecular Genetics &Genomic Medicine, Volume 13, Issue 6, June 2025.A novel synonymous variant of PAX2 in monochorionic diamniotic twins with bilateral renal dysplasia was demonstrated to be associated with PAX2‐disorders through the integration of clinical findings and minigene assay results. ABSTRACT Background Paired Box 2 (PAX2, NM_000278.5) encodes paired box gene 2, one of many human homologs of the Drosophila ...
Wencong Yao +8 more
wiley +1 more source
Journal of the Royal Anthropological Institute, Volume 31, Issue 1, Page 264-282, March 2025.This article demonstrates the important role family narratives can play in providing ethical, person‐centred support for people with severe intellectual disabilities living in supported accommodation. Focusing on the story of Daniel, a 65‐year‐old man residing in a group home in Australia, I illustrate, through the lens of his mother Arleen, how family
Aaron J. Jackson
wiley +1 more source
Acta Paediatrica, Volume 114, Issue 3, Page 619-627, March 2025.Abstract Aim This qualitative study explored the lived experiences of the patients with microphthalmia and anophthalmia and their parents, focusing on the healthcare, school settings and daily life challenges to improve patient management. Methods In‐depth interviews were conducted in Stockholm, Sweden, from October 2022 to June 2023. Participants were
Evin Chireh +3 more
wiley +1 more source
The Pan African Medical Journal, 2017 Le syndrome dit Morning glory ou à belle de jourà est une anomalie congénitale rare de la papille par émergence du nerf optique dans l'oeil. Il est parfois associé à des anomalies graves du système nerveux central.
Napo Abdoulaye, Sidibe Mohamed Kole
doaj +1 more source
Ecology and Evolution, 2019 The frequent transition from outcrossing to selfing in flowering plants is often accompanied by changes in multiple aspects of floral morphology, termed the “selfing syndrome.” While the repeated evolution of these changes suggests a role for natural ...
Joanna L. Rifkin +3 more
doaj +1 more source
Morning Glory Syndrome, Amaurosis Fugax, and Cortical Laser Tomography
, 1995 Morning Glory Syndrome was identified in the left eye of an 18 yr.-old patient whose only complaint was the presence of amaurosis fogax in the left eye during the last year period with 3-4 episodes a month, lasting up to 20 minutes each ...
Roberto Ebner, MD
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