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1
المؤلفون: Rafael Navarro, Mark S. Blumenkranz, Brett J. Rosenblatt, David A. Fastenberg, Steven R. Sanislo, Fred Y. Chien, Carlos Mateo, Mauricio A Lopez, Vincent A. Deramo, Shawn M. Ronan, Stephen J. Saxe, Darius M. Moshfeghi, Susan G. Elner, Iñigo A. Corcóstegui, Pradeepa Yoganathan, Mark W. Johnson, David N. Zacks
المصدر: Retina. 27:535-540
مصطلحات موضوعية: Male, Vascular Endothelial Growth Factor A, medicine.medical_specialty, genetic structures, Bevacizumab, Angiogenesis Inhibitors, Antibodies, Monoclonal, Humanized, Injections, Macular Degeneration, chemistry.chemical_compound, Ophthalmology, Humans, Medicine, Fluorescein Angiography, Pigment Epithelium of Eye, Aged, Retrospective Studies, Aged, 80 and over, Retina, Retinal pigment epithelium, medicine.diagnostic_test, business.industry, Retinal Detachment, Antibodies, Monoclonal, Retinal, General Medicine, Macular degeneration, Retinal Perforations, Fluorescein angiography, medicine.disease, Choroidal Neovascularization, eye diseases, Vitreous Body, medicine.anatomical_structure, chemistry, Tears, Female, sense organs, Ranibizumab, business, Tomography, Optical Coherence, medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::150291a1361c56d08b0fe4d77ee437fe
https://doi.org/10.1097/iae.0b013e3180cc2645 -
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المؤلفون: Larry D. Atwood, Douglas J. Wilkin, Terri L. Young, William S. Oetting, Scott C. Wildenberg, Shawn M. Ronan, Richard A. King, Alison B. Alvear
المصدر: The American Journal of Human Genetics. 63(5):1419-1424
مصطلحات موضوعية: Adult, Genetic Markers, Male, Marfan syndrome, genetic structures, Glaucoma, Locus (genetics), Marfan Syndrome, Gene mapping, Genetic linkage, Germany, medicine, Myopia, Genetics, Humans, Chromosome 12q, Genetics(clinical), Pathologic myopia, Age of Onset, Child, Genetics (clinical), Aged, Recombination, Genetic, Chromosomal mapping, Chromosomes, Human, Pair 12, business.industry, Genetic heterogeneity, Chromosome Mapping, Middle Aged, medicine.disease, Introns, United States, eye diseases, Pedigree, Autosomal dominant, Italy, Child, Preschool, Eye disorder, Female, sense organs, Age of onset, business, Linkage analysis, Research Article
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3
المؤلفون: Richard A. King, Terri L. Young, Shawn M. Ronan, Larry D. Atwood, William S. Oetting, Scott C. Wildenberg, Douglas J. Wilkin, Alison B. Alvear, Leslie A. Drahozal
المصدر: The American Journal of Human Genetics. 63(1):109-119
مصطلحات موضوعية: Male, Marfan syndrome, Chromosome 18p, genetic structures, Genetic Linkage, Locus (genetics), Biology, Eye, Genetic determinism, Marfan Syndrome, Gene mapping, Genetic linkage, Myopia, medicine, Genetics, Humans, Stickler syndrome, Genetics(clinical), Genetics (clinical), Genes, Dominant, Haplotype, Chromosome Mapping, Chromosome, Glaucoma, medicine.disease, eye diseases, Pedigree, Autosomal dominant, Haplotypes, Female, sense organs, Lod Score, Chromosomes, Human, Pair 18, Linkage analysis, Microsatellite Repeats, Research Article
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4
المؤلفون: Jonathan T. Pribila, Jonathan D Trobe, Shawn M. Ronan
المصدر: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society. 28(1)
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, genetic structures, medicine.medical_treatment, Optic Disk, Vision, Low, Nevoid basal-cell carcinoma syndrome, Craniospinal Irradiation, Neurosurgical Procedures, Retina, Meningioma, Neoplasms, Multiple Primary, Meninges, medicine, Humans, Embolization, Papilledema, neoplasms, Medulloblastoma, Radiotherapy, business.industry, Brain Neoplasms, Basal Cell Nevus Syndrome, medicine.disease, Magnetic Resonance Imaging, eye diseases, nervous system diseases, stomatognathic diseases, Ophthalmology, Treatment Outcome, Disease Progression, Neurology (clinical), Radiology, medicine.symptom, Intracranial Hypertension, business, Visual dysfunction, Craniospinal
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42190ce10c6c6dd1d9111ff09cd67c11
https://pubmed.ncbi.nlm.nih.gov/18347458 -
5
المؤلفون: Outi Mäkitie, Shawn M. Ronan, Scott C. Wildenberg, Prasuna Paluru, Terri L. Young, William G. Cole, Marcella Devoto, Ann M. Holleschau, Elise Heon, Richard A. King, Genaro S. Scavello
المصدر: Investigative ophthalmologyvisual science. 44(5)
مصطلحات موضوعية: Male, Genotype, Genetic Linkage, Quantitative Trait Loci, Locus (genetics), Biology, medicine, Myopia, Humans, Severe Myopia, Stickler syndrome, Child, Allele frequency, Genes, Dominant, Genetics, Genetic heterogeneity, Haplotype, Chromosome Mapping, medicine.disease, Penetrance, eye diseases, Pedigree, Child, Preschool, Microsatellite, Female, Lod Score, Chromosomes, Human, Pair 17, Microsatellite Repeats
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f6a49bb89934f9e8fff2a1fcdaf0516
https://pubmed.ncbi.nlm.nih.gov/12714612 -
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المؤلفون: Terri L. Young, Larry D. Atwood, Shawn M. Ronan, Anthony T. Dewan, Alison B. Alvear, Richard A. King, Ann M. Holleschau, Janice Peterson
المصدر: Ophthalmic genetics. 22(2)
مصطلحات موضوعية: Genetics, Genetic Markers, Linkage disequilibrium, genetic structures, Genotype, Haplotype, Locus (genetics), Biology, Physical Chromosome Mapping, eye diseases, Linkage Disequilibrium, Pedigree, Ophthalmology, Centimorgan, Genetic epidemiology, Haplotypes, Genetic linkage, Genetic marker, Pediatrics, Perinatology and Child Health, Myopia, Humans, Allele, Chromosomes, Human, Pair 18, Genetics (clinical), Genes, Dominant
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المؤلفون: Shawn M. Ronan, Terri L. Young, William S. Oetting, Thomas A. Sellers, Richard A. King, Catherine M. Armstrong
المصدر: Electrophoresis. 19(18)
مصطلحات موضوعية: Genetics, Genetic Markers, Polymorphism, Genetic, Spectrophotometry, Infrared, Clinical Biochemistry, Sequence Analysis, DNA, Biology, Biochemistry, Analytical Chemistry, law.invention, DNA sequencer, Spectrometry, Fluorescence, Gene mapping, law, Short Tandem Repeat Polymorphism, Genetic marker, Tandem Repeat Sequences, Multiplex polymerase chain reaction, Microsatellite, Humans, Primer (molecular biology), Polymerase chain reaction, DNA Primers
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8
المؤلفون: Shawn M. Ronan, Terri L. Young, Khanh-Nhat Tran-Viet, Cynthia A. Toth, Erica Burner, Ravikanth Metlapally
المصدر: Archives of Ophthalmology. 127:1511
مصطلحات موضوعية: Adult, Male, Proband, Adolescent, Eye Diseases, DNA Mutational Analysis, Biology, Polymerase Chain Reaction, Article, Exon, Versicans, medicine, Humans, Stickler syndrome, Allele, Child, Base Pairing, Collagen Type II, Gene, Genetics, Splice site mutation, Point mutation, Retinal Degeneration, DNA, Syndrome, Middle Aged, medicine.disease, Pedigree, Vitreous Body, Ophthalmology, Mutation, Female, Tomography, Optical Coherence
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e83d82a1e0a8fdd6303c9040cc2a08a
https://doi.org/10.1001/archophthalmol.2009.273 -
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المؤلفون: Shawn M. Ronan, Hakan Demirci, Deborah Y. Chong, Andrew Flint, Victor M. Elner
المصدر: Archives of Ophthalmology. 125:566
مصطلحات موضوعية: Male, Orbital rhabdomyosarcoma, Pathology, medicine.medical_specialty, business.industry, Infant, Exons, Genes, p53, medicine.disease, Magnetic Resonance Imaging, Polymerase Chain Reaction, Li-Fraumeni Syndrome, Ophthalmology, X ray computed, Li–Fraumeni syndrome, Rhabdomyosarcoma, Humans, Orbital Neoplasms, Medicine, Tomography, X-Ray Computed, business, Germ-Line Mutation
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efb2e1f7a6b7f2eb1d6c6f236299679e
https://doi.org/10.1001/archopht.125.4.566 -
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المؤلفون: Marcia S. Brott, Larry D. Atwood, William S. Oetting, Takaaki Hayashi, Richard A. King, Shawn M. Ronan, Nancy Benegas, Terri L. Young, Ann M. Holleschau, Genaro S. Scavello, Alison B. Alvear, Arno G. Motulsky, Samir S. Deeb, Thomas Rosenberg, Marianne Schwartz, Prasuna Paluru, Andrew T. DeWan
المصدر: Archives of Ophthalmology. 122:897
مصطلحات موضوعية: Adult, Male, Adolescent, Genotype, Genetic Linkage, DNA Mutational Analysis, Color Vision Defects, Locus (genetics), Biology, Polymerase Chain Reaction, Deuteranopia, Centimorgan, Electroretinography, Myopia, medicine, Humans, Color perception test, Age of Onset, Child, Eye Proteins, X-linked recessive inheritance, Genetics, Color Perception Tests, medicine.diagnostic_test, Haplotype, Rod Opsins, Chromosome Mapping, Genetic Diseases, X-Linked, Pedigree, Xq28, Blotting, Southern, Ophthalmology, Haplotypes, OPN1LW, Child, Preschool, Retinal Cone Photoreceptor Cells, Female
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b16a507f351349be2bc3fef52b46c74
https://doi.org/10.1001/archopht.122.6.897