Results 121 to 130 of about 57,799 (256)
Blindness and visual impairment in retinitis pigmentosa: a Cameroonian hospital-based study
, 2010 André Omgbwa Eballe1, Godefroy Koki2, Claude Bernard Emche2, Lucienne Assumpta Bella2, Jeanne Mayouego Kouam2, Justin Melong31Faculty of Medicine and Pharmaceutical Sciences, University of Douala; 2Faculty of Medicine and Biomedical Sciences ...
Claude Bernard Emche +3 more
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: Peropsin in retinitis pigmentosa
, 2007 Many genes from retinoid metabolism cause retinitis pigmentosa. Peropsin, an opsin-like protein with unknown function, is specifically expressed in apical retinal pigment epithelium microvilli.
Hamel, Christian, P. +5 more
core +1 more source
Targeting Mitochondria in Aging‐Related Diseases: Therapeutic Potential and Obstacles
MedComm, Volume 7, Issue 6, June 2026.This article systematically summarized the specific mechanism of aging‐related diseases caused by mitochondrial dysfunction, and summarized the broad‐spectrum treatment methods and disease targeted treatment strategies for mitochondria. At the same time, it also pointed out the dilemma faced by mitochondrial targeted treatment.
Zijie Xiang +12 more
wiley +1 more source
Human Retinal Organoid Model of Ocular Toxoplasmosis
PathogensThe health burden of ocular toxoplasmosis is substantial, and there is an unmet need for safe and curative anti-microbial drugs. One major barrier to research on new therapeutics is the lack of in vitro human-based models beyond two-dimensional cultured ...
Liam M. Ashander +5 more
doaj +1 more source
, 2014 Retinitis pigmentosa is a retinal/choroidal degeneration caused by various genetic defects. The term retinitis pigmentosa is really a misnomer since it is not inflammation (retinitis) and it is not a disease of the pigmentary system (pigmentosa)
Gregory P. Van Stavern, MD
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Nano Select, Volume 7, Issue 6, June 2026.The introduction covers the background and significance of conjunctivitis. It continues with a review of etiology, epidemiology, and clinical manifestations. Diagnostic methods are described, followed by discussions on pathophysiology and classification. Current treatment strategies, preventive measures, and therapeutic challenges are analyzed.
Xia Linkang +11 more
wiley +1 more source
Neuropsychopharmacology Reports, Volume 46, Issue 2, June 2026.Mitochondrial dysfunction is implicated in depression, and a pillow‐based ELF‐ELME device for nighttime use improved depressive symptoms in a preliminary 8‐week open‐label study of MDD without adverse events. This non‐invasive intervention may offer a safe and feasible adjunctive treatment option.
Ibuki Tomita +9 more
wiley +1 more source
, 1897 RETINITIS HAEMORRHAGICA Retinitis haemorrhagica ([1]) Binding ( - ) Title page ([1]) Chapter ([3]) Section (21) Vita. ( - ) Binding ( -
Hotzen, Friedrich
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The Journal of Pathology, Volume 269, Issue 2, Page 222-231, June 2026.Abstract MYO7A is a causal gene, underlying Usher syndrome type 1B (USH1B) and both autosomal recessive (DFNB2) and dominant (DFNA11) non‐syndromic hearing loss. Despite the large number of reported MYO7A variants (over 2,200), variants located in an extended splice region remain difficult to interpret and are often classified as variants of uncertain ...
Tao Shi +5 more
wiley +1 more source