-
1دورية أكاديمية
المؤلفون: Hao XD; Institute for Translational Medicine, the Affiliated Hospital of Qingdao University, College of Medicine, Qingdao University, Qingdao 266021, China. Electronic address: haoxiaodan@qdu.edu.cn., Liu JX; Institute for Translational Medicine, the Affiliated Hospital of Qingdao University, College of Medicine, Qingdao University, Qingdao 266021, China., Zhang JS; Institute for Translational Medicine, the Affiliated Hospital of Qingdao University, College of Medicine, Qingdao University, Qingdao 266021, China.
المصدر: Life sciences [Life Sci] 2024 Aug 01; Vol. 350, pp. 122769. Date of Electronic Publication: 2024 Jun 06.
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 0375521 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0631 (Electronic) Linking ISSN: 00243205 NLM ISO Abbreviation: Life Sci Subsets: MEDLINE
مواضيع طبية MeSH: Forkhead Box Protein O3*/metabolism , Eye Diseases*/metabolism , Eye Diseases*/drug therapy , Aging*/metabolism, Humans ; Animals ; Longevity
-
2دورية أكاديمية
المؤلفون: Owete AC; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA., Ionin R; National Institutes of Health Library, National Institutes of Health, Bethesda, MD, USA., Huryn LA; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA., Cukras CA; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA., Blain D; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA., Agather AR; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA., Hufnagel RB; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA., Brooks BP; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA., Nwanyanwu K; Department of Ophthalmology and Visual Science, Yale School of Medicine, New Haven, CT, USA., Zein WM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA.
المصدر: Translational vision science & technology [Transl Vis Sci Technol] 2024 Sep 03; Vol. 13 (9), pp. 4.
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Association for Research in Vision and Ophthalmology Country of Publication: United States NLM ID: 101595919 Publication Model: Print Cited Medium: Internet ISSN: 2164-2591 (Electronic) Linking ISSN: 21642591 NLM ISO Abbreviation: Transl Vis Sci Technol Subsets: MEDLINE
مواضيع طبية MeSH: Black or African American*/genetics , Eye Diseases, Hereditary*/genetics , Eye Diseases, Hereditary*/ethnology, Humans ; Genomics/methods
-
3دورية أكاديمية
المؤلفون: Tsur A; Department of Rehabilitation, Galilee Medical Center, Nahariya, Affiliated to the Azrieli Faculty of Medicine of Bar-Ilan at Zfat., Volpin G; Department of Orthopedics, Galilee Medical Center, Nahariya, Affiliated to the Azrieli Faculty of Medicine of Bar-Ilan at Zfat., Segal Z; Department of Ophthalmology, Galilee Medical Center, Nahariya, Affiliated to the Azrieli Faculty of Medicine of Bar-Ilan at Zfat.
المصدر: Harefuah [Harefuah] 2024 Sep; Vol. 163 (9), pp. 585-588.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Israel Medical Association Country of Publication: Israel NLM ID: 0034351 Publication Model: Print Cited Medium: Print ISSN: 0017-7768 (Print) Linking ISSN: 00177768 NLM ISO Abbreviation: Harefuah Subsets: MEDLINE
مواضيع طبية MeSH: Accidental Falls*/statistics & numerical data , Accidental Falls*/prevention & control , Hip Fractures*/epidemiology , Hip Fractures*/etiology , Eyeglasses* , Eye Diseases*/etiology , Eye Diseases*/epidemiology, Humans ; Male ; Female ; Aged ; Aged, 80 and over ; Age Factors ; Cataract/epidemiology
-
4دورية أكاديمية
المصدر: Human gene therapy [Hum Gene Ther] 2024 Sep; Vol. 35 (17-18), pp. 583-584.
نوع المنشور: Editorial; Journal Article
بيانات الدورية: Publisher: M.A. Liebert Country of Publication: United States NLM ID: 9008950 Publication Model: Print Cited Medium: Internet ISSN: 1557-7422 (Electronic) Linking ISSN: 10430342 NLM ISO Abbreviation: Hum Gene Ther Subsets: MEDLINE
مواضيع طبية MeSH: Genetic Therapy*/methods , Genetic Therapy*/trends , Eye Diseases*/therapy , Eye Diseases*/genetics, Humans
-
5دورية أكاديمية
المؤلفون: Russell MW; Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, USA.; Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA., Kumar M; Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA.; Case Western Reserve University School of Medicine, Cleveland, OH, USA., Li A; Cleveland Clinic Cole Eye Institute, Cleveland, OH, USA., Singh RP; Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA.; Cleveland Clinic Cole Eye Institute, Cleveland, OH, USA.; Martin North Hospital, Cleveland Clinic, FL, USA., Talcott KE; Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA. Talcotk@ccf.org.; Cleveland Clinic Cole Eye Institute, Cleveland, OH, USA. Talcotk@ccf.org.
المصدر: Eye (London, England) [Eye (Lond)] 2024 Sep; Vol. 38 (13), pp. 2603-2609. Date of Electronic Publication: 2024 Apr 27.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 8703986 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5454 (Electronic) Linking ISSN: 0950222X NLM ISO Abbreviation: Eye (Lond) Subsets: MEDLINE
مواضيع طبية MeSH: Obesity, Morbid*/surgery , Obesity, Morbid*/epidemiology , Obesity, Morbid*/complications , Bariatric Surgery*/adverse effects , Databases, Factual* , Eye Diseases*/epidemiology , Eye Diseases*/etiology, Humans ; Male ; Retrospective Studies ; Female ; United States/epidemiology ; Incidence ; Middle Aged ; Adult ; Aged ; Postoperative Complications/epidemiology ; Diabetic Retinopathy/epidemiology ; Glaucoma/epidemiology ; Macular Degeneration/epidemiology ; Macular Degeneration/etiology ; Blindness/epidemiology ; Blindness/etiology
-
6دورية أكاديمية
المؤلفون: Gupta C; Shroff Eye Centre, A-9, Kailash Colony, New Delhi 110048, India., Kumar S; Shroff Eye Centre, A-9, Kailash Colony, New Delhi 110048, India. Electronic address: guptasandeep.901@gmail.com., Shroff D; Shroff Eye Centre, A-9, Kailash Colony, New Delhi 110048, India.
المصدر: Journal francais d'ophtalmologie [J Fr Ophtalmol] 2024 Sep; Vol. 47 (7), pp. 104220. Date of Electronic Publication: 2024 Jun 04.
نوع المنشور: Case Reports; Journal Article; Letter
بيانات الدورية: Publisher: Masson Country of Publication: France NLM ID: 7804128 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1773-0597 (Electronic) Linking ISSN: 01815512 NLM ISO Abbreviation: J Fr Ophtalmol Subsets: MEDLINE
مواضيع طبية MeSH: Tomography, Optical Coherence*/methods , Familial Exudative Vitreoretinopathies*/diagnosis , Fluorescein Angiography*/methods , Eye Diseases, Hereditary*/diagnosis , Eye Diseases, Hereditary*/pathology , Eye Diseases, Hereditary*/diagnostic imaging, Humans ; Retinal Diseases/diagnosis ; Retinal Diseases/diagnostic imaging ; Retinal Diseases/pathology ; Male ; Female
-
7دورية أكاديمية
المؤلفون: Zhang X; Department of Ophthalmology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, China., Yang L; Harbin Purui Eye Hospital, Harbin, China., Wang F; Department of Ophthalmology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, China. wangfd@126.com., Su Y; Eye Hospital, The first affiliated hospital of Harbin Medical University, Harbin, China. suying0511@126.com.
المصدر: Human cell [Hum Cell] 2024 Sep; Vol. 37 (5), pp. 1336-1346. Date of Electronic Publication: 2024 Aug 02.
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Springer Country of Publication: Japan NLM ID: 8912329 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1749-0774 (Electronic) Linking ISSN: 09147470 NLM ISO Abbreviation: Hum Cell Subsets: MEDLINE
مواضيع طبية MeSH: Quantum Dots* , Carbon* , Eye Diseases*/diagnosis , Eye Diseases*/therapy, Humans ; Drug Delivery Systems
-
8دورية أكاديمية
المؤلفون: Katta M; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Genetics Department, Moorfields Eye Hospital, London, United Kingdom., de Guimaraes TAC; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Genetics Department, Moorfields Eye Hospital, London, United Kingdom., Fujinami-Yokokawa Y; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Laboratory of Visual Physiology, Division of Vision Research, National Institute of Sensory Organs, NHO Tokyo Medical Center, Tokyo, Japan; Department of Health Policy and Management, Keio University School of Medicine, Tokyo, Japan., Fujinami K; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Genetics Department, Moorfields Eye Hospital, London, United Kingdom; Laboratory of Visual Physiology, Division of Vision Research, National Institute of Sensory Organs, NHO Tokyo Medical Center, Tokyo, Japan., Georgiou M; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Genetics Department, Moorfields Eye Hospital, London, United Kingdom; Jones Eye Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas., Mahroo OA; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Genetics Department, Moorfields Eye Hospital, London, United Kingdom., Webster AR; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Genetics Department, Moorfields Eye Hospital, London, United Kingdom., Michaelides M; UCL Institute of Ophthalmology, University College London, London, United Kingdom; Genetics Department, Moorfields Eye Hospital, London, United Kingdom. Electronic address: michel.michaelides@ucl.ac.uk.
المصدر: Ophthalmology. Retina [Ophthalmol Retina] 2024 Sep; Vol. 8 (9), pp. 932-941. Date of Electronic Publication: 2024 Mar 24.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Published by Elsevier Inc. on behalf of American Academy of Ophthalmology Country of Publication: United States NLM ID: 101695048 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2468-6530 (Electronic) Linking ISSN: 24686530 NLM ISO Abbreviation: Ophthalmol Retina Subsets: MEDLINE
مواضيع طبية MeSH: Night Blindness*/genetics , Night Blindness*/diagnosis , Night Blindness*/physiopathology , Myopia*/genetics , Myopia*/physiopathology , Myopia*/diagnosis , Tomography, Optical Coherence*/methods , Eye Diseases, Hereditary*/genetics , Eye Diseases, Hereditary*/diagnosis , Eye Diseases, Hereditary*/physiopathology , Genetic Diseases, X-Linked*/genetics , Genetic Diseases, X-Linked*/physiopathology , Genetic Diseases, X-Linked*/diagnosis, Humans ; Male ; Retrospective Studies ; Female ; Child ; Child, Preschool ; Adolescent ; Adult ; Genetic Association Studies/methods ; Young Adult ; Visual Acuity ; Follow-Up Studies ; Genotype ; Mutation ; Phenotype ; Middle Aged ; Electroretinography/methods ; Infant ; Retinal Ganglion Cells/pathology ; DNA/genetics
SCR Disease Name: Night blindness, congenital stationary
-
9دورية أكاديمية
المؤلفون: Havrylov S; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.; Department of Ophthalmology, 829 Medical Sciences Building, University of Alberta, Edmonton, AB, T6G 2H7, Canada., Chrystal P; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.; Department of Ophthalmology, 829 Medical Sciences Building, University of Alberta, Edmonton, AB, T6G 2H7, Canada., van Baarle S; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.; Department of Ophthalmology, 829 Medical Sciences Building, University of Alberta, Edmonton, AB, T6G 2H7, Canada., French CR; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.; Department of Ophthalmology, 829 Medical Sciences Building, University of Alberta, Edmonton, AB, T6G 2H7, Canada.; Faculty of Medicine, Memorial University, St. John's, NL, Canada., MacDonald IM; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.; Department of Ophthalmology, 829 Medical Sciences Building, University of Alberta, Edmonton, AB, T6G 2H7, Canada., Avasarala J; Department of Neurology, University of Kentucky Medical Center, Lexington, KY, USA., Rogers RC; Greenwood Genetic Center, Greenwood, SC, USA., Berry FB; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada.; Department of Surgery, 3002D Li Ka Shing Centre, University of Alberta, Edmonton, AB, Canada., Kume T; Feinberg Cardiovascular Research Institute, Feinberg School of Medicine, Northwestern University, Chicago, USA., Waskiewicz AJ; Department of Biological Sciences, University of Alberta, Edmonton, AB, Canada., Lehmann OJ; Department of Medical Genetics, University of Alberta, Edmonton, AB, Canada. olehmann@ualberta.ca.; Department of Ophthalmology, 829 Medical Sciences Building, University of Alberta, Edmonton, AB, T6G 2H7, Canada. olehmann@ualberta.ca.
المصدر: Scientific reports [Sci Rep] 2024 Aug 31; Vol. 14 (1), pp. 20278. Date of Electronic Publication: 2024 Aug 31.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
مواضيع طبية MeSH: Cilia*/metabolism , Cilia*/pathology , Forkhead Transcription Factors*/metabolism , Forkhead Transcription Factors*/genetics , Signal Transduction* , Phenotype* , Eye Abnormalities*/genetics , Eye Abnormalities*/pathology , Eye Abnormalities*/metabolism , Eye Diseases, Hereditary*/genetics , Eye Diseases, Hereditary*/metabolism , Eye Diseases, Hereditary*/pathology, Humans ; Animals ; Mice ; Hedgehog Proteins/metabolism ; Hedgehog Proteins/genetics ; Anterior Eye Segment/abnormalities ; Anterior Eye Segment/metabolism ; Anterior Eye Segment/pathology ; Receptor, Platelet-Derived Growth Factor alpha/metabolism ; Receptor, Platelet-Derived Growth Factor alpha/genetics ; Ciliopathies/genetics ; Ciliopathies/metabolism ; Ciliopathies/pathology ; Female ; Male ; Zinc Finger Protein Gli2/metabolism ; Zinc Finger Protein Gli2/genetics ; Mutation
SCR Disease Name: Axenfeld-Rieger syndrome
-
10دورية أكاديمية
المؤلفون: Su Y; Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.; Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai 200011, China., Chen M; Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.; Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai 200011, China., Xu W; Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.; Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai 200011, China., Gu P; Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.; Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai 200011, China., Fan X; Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.; Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai 200011, China.
المصدر: ACS nano [ACS Nano] 2024 Aug 27; Vol. 18 (34), pp. 22793-22828. Date of Electronic Publication: 2024 Aug 14.
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 101313589 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1936-086X (Electronic) Linking ISSN: 19360851 NLM ISO Abbreviation: ACS Nano Subsets: MEDLINE