المؤلفون: Lagan Paul, Sumit Kumar, Shalini Singh, Tanya Jain

المصدر: BMC Ophthalmology, Vol 20, Iss 1, Pp 1-5 (2020)

مصطلحات موضوعية: Case report, Lebers congenital amaurosis (LCA), Retinal astrocytic hamartomas (RAHs), Inherited retinal disorder (IRD), Ophthalmology, RE1-994

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s12886-020-01646-zTest; https://doaj.org/toc/1471-2415Test

الوصول الحر: https://doaj.org/article/c9762ead160b410d934c56b48241d0aaTest

المؤلفون: Mònica Berges-Marti, Laura Distefano, Eric Kirkegaard-Biosca, José García-Arumí, Brahim Azarfane, Esther Cilveti

المساهمون: Institut Català de la Salut, [Kirkegaard-Biosca E, Berges-Marti M, Azarfane B, Distefano L] Servei d’Oftalmologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Cilveti E] Servei d’Oftalmologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Ophthalmology Department, Moises Broggi Hospital, Barcelona, Spain. [García-Arumí J] Servei d’Oftalmologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Department of Retina and Vitreous, Instituto de Microcirugía Ocular (IMO), Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: BMC Ophthalmology
Scientia
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-6 (2021)

مصطلحات موضوعية: Fundus flavimaculatus, medicine.medical_specialty, Retinal Disorder, genetic structures, Myotonic dystrophy, Posterior pole, Vision Disorders, Case Report, Fundus (eye), Retina, Otros calificadores::Otros calificadores::/complicaciones [Otros calificadores], 03 medical and health sciences, 0302 clinical medicine, Ptosis, Ophthalmology, Humans, Stargardt Disease, Medicine, business.industry, Dystrophy, General Medicine, RE1-994, medicine.disease, Myotonia, Pattern dystrophy, eye diseases, enfermedades musculoesqueléticas::enfermedades musculares::trastornos musculares atróficos::distrofias musculares::distrofia miotónica [ENFERMEDADES], Phenotype, medicine.anatomical_structure, Musculoskeletal Diseases::Muscular Diseases::Muscular Disorders, Atrophic::Muscular Dystrophies::Myotonic Dystrophy [DISEASES], Nervous System Diseases::Neurologic Manifestations::Sensation Disorders::Vision Disorders [DISEASES], Distròfia muscular - Complicacions, 030221 ophthalmology & optometry, Female, sense organs, medicine.symptom, business, Degeneració macular, 030217 neurology & neurosurgery, Other subheadings::Other subheadings::/complications [Other subheadings], enfermedades del sistema nervioso::manifestaciones neurológicas::trastornos sensoriales::trastornos de la visión [ENFERMEDADES]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ea1aef27ecb565331fd013c09a59255Test
https://doi.org/10.1186/s12886-021-02002-5Test

المؤلفون: Elli V. Kostopoulou, Olga E Makri, Constantine D. Georgakopoulos, Foteini Tsapardoni

المصدر: BMC Ophthalmology
BMC Ophthalmology, Vol 18, Iss 1, Pp 1-9 (2018)

مصطلحات موضوعية: medicine.medical_specialty, Pediatrics, Retinal Disorder, Thalassemia, Siderophores, Case Report, Hemosiderosis, Deferoxamine, Infusions, Subcutaneous, Retina, Drug toxicity, 03 medical and health sciences, 0302 clinical medicine, lcsh:Ophthalmology, Internal medicine, Electroretinography, medicine, Humans, Chelation therapy, Dose Modification, Hematology, business.industry, Retinal Degeneration, General Medicine, Middle Aged, medicine.disease, Pattern dystrophy, Discontinuation, Ophthalmology, lcsh:RE1-994, 030221 ophthalmology & optometry, Female, sense organs, business, Tomography, Optical Coherence, 030217 neurology & neurosurgery, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ee8a2653221453fc6845392f75cbfafTest
https://doi.org/10.1186/s12886-018-0911-2Test

المؤلفون: Shankar Khanal, Govinda Paudyal, Suman S Thapa, Stevie Tan, Sanyam Bajimaya, G.H.M.B. van Rens, Raba Thapa

المساهمون: Ophthalmology, APH - Societal Participation & Health, APH - Quality of Care, Amsterdam Reproduction & Development (AR&D)

المصدر: Thapa, R, Bajimaya, S, Paudyal, G, Khanal, S, Tan, S, Thapa, S S & van Rens, G H M B 2018, ' Prevalence and causes of low vision and blindness in an elderly population in Nepal: The Bhaktapur retina study ', BMC Ophthalmology, vol. 18, no. 1, 42 . https://doi.org/10.1186/s12886-018-0710-9Test
BMC Ophthalmology, Vol 18, Iss 1, Pp 1-10 (2018)
BMC Ophthalmology, 18(1):42. BioMed Central
BMC Ophthalmology

مصطلحات موضوعية: Male, Pediatrics, Refractive error, genetic structures, Visual Acuity, Blindness, chemistry.chemical_compound, Elderly, 0302 clinical medicine, lcsh:Ophthalmology, Risk Factors, Surveys and Questionnaires, Prevalence, 030212 general & internal medicine, Low vision, Aged, 80 and over, education.field_of_study, General Medicine, Middle Aged, Refractive Errors, Female, medicine.symptom, Visually Impaired Persons, Research Article, medicine.medical_specialty, Retinal Disorder, Visual impairment, Population, Vision, Low, Refraction, Ocular, Cataract, 03 medical and health sciences, Age Distribution, Retinal Diseases, Nepal, medicine, Humans, Sex Distribution, education, Aged, business.industry, Retinal, medicine.disease, Subjective refraction, eye diseases, Confidence interval, Posterior segment of eyeball, Ophthalmology, Cross-Sectional Studies, chemistry, lcsh:RE1-994, 030221 ophthalmology & optometry, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::421e197415a2e3a69ef9b1403b16888eTest
https://doi.org/10.1186/s12886-018-0710-9Test

المؤلفون: Leera D’Souza, Keith Wetherby, Xinjing Wang, Wadih M. Zein, Yang C. Fann, Amy Turriff, Chimere Roberson, Kory R. Johnson, Hong He, Angela Villarta

المصدر: BMC Ophthalmology, Vol 17, Iss 1, Pp 1-15 (2017)
BMC Ophthalmology

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Proband, Retinal Disorder, DNA Mutational Analysis, Context (language use), Computational biology, 030105 genetics & heredity, Polymerase Chain Reaction, Mutation screening, DNA sequencing, 03 medical and health sciences, chemistry.chemical_compound, Genotype-phenotype distinction, lcsh:Ophthalmology, Retinal Dystrophies, Retinal, Humans, Medicine, Genetic Predisposition to Disease, Next-generation-sequencing, Aged, business.industry, General Medicine, Middle Aged, Amplicon, Microdroplet PCR, Ophthalmology, 030104 developmental biology, chemistry, lcsh:RE1-994, Mutation, Female, business, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffcb5e5be5c3c496149b60903834e0b0Test
https://doi.org/10.1186/s12886-017-0549-5Test