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  • 1-10 ل  68 نتائج ل ""Microphthalmos""
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Academic Journal

Prevalence of complications in eyes with nanophthalmos or microphthalmos: protocol for a systematic review and meta-analysis.

  • Authors : Ally N; Department of Neurosciences, Division of Ophthalmology, University of the Witwatersrand, 7 York Road, Parktown, Johannesburg, Gauteng, 2193, South Africa. .; Ismail S

Subjects: Hyperopia*/Hyperopia*/Hyperopia*/complications ; Hyperopia*/Hyperopia*/Hyperopia*/diagnosis ; Hyperopia*/Hyperopia*/Hyperopia*/epidemiology

  • Source: Systematic reviews [Syst Rev] 2022 Feb 09; Vol. 11 (1), pp. 25. Date of Electronic Publication: 2022 Feb 09.Publisher: BioMed Central Country of Publication: England NLM ID: 101580575 Publication Model: Electronic Cited Medium: Internet ISSN: 2046-4053

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Academic Journal

Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse.

  • Authors : Hassall MM; Department of Ophthalmology, Flinders University, Bedford Park, SA, Australia. .; Javadiyan S

Subjects: Glaucoma, Angle-Closure*/Glaucoma, Angle-Closure*/Glaucoma, Angle-Closure*/pathology ; Hyperopia*/Hyperopia*/Hyperopia*/genetics ; Hyperopia*/Hyperopia*/Hyperopia*/complications

  • Source: Scientific reports [Sci Rep] 2023 Jul 07; Vol. 13 (1), pp. 11017. Date of Electronic Publication: 2023 Jul 07.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Editorial & Opinion

Posterior microphthalmos versus nanophthalmos.

Subjects: Hyperopia/Hyperopia/Hyperopia/*embryology ; Hyperopia/Hyperopia/Hyperopia/*physiopathology ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2008 Dec; Vol. 29 (4), pp. 189.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print Cited Medium: Internet ISSN: 1744-5094

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Academic Journal

Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.

Subjects: Glaucoma, Angle-Closure/Glaucoma, Angle-Closure/Glaucoma, Angle-Closure/*genetics ; Hyperopia/Hyperopia/Hyperopia/*genetics ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics Nanophthalmos 1

  • Source: PLoS genetics [PLoS Genet] 2019 May 02; Vol. 15 (5), pp. e1008130. Date of Electronic Publication: 2019 May 02 (Print Publication: 2019).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort.

  • Authors : Prasov L; Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, 48105, USA. .; Department of Human Genetics, University of Michigan, Ann Arbor, MI, 48109, USA. .

Subjects: Eye Diseases, Hereditary/Eye Diseases, Hereditary/Eye Diseases, Hereditary/*genetics ; Frameshift Mutation/Frameshift Mutation/Frameshift Mutation/*genetics ; Hyperopia/Hyperopia/Hyperopia/*genetics Hyperopia, High

  • Source: Scientific reports [Sci Rep] 2020 Nov 17; Vol. 10 (1), pp. 19986. Date of Electronic Publication: 2020 Nov 17.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Novel membrane frizzled-related protein gene mutation as cause of posterior microphthalmia resulting in high hyperopia with macular folds.

  • Authors : Wasmann RA; Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen, The NetherlandsDepartment of Clinical Genetics, University of Groningen, University Medical Center Groningen, Groningen, The NetherlandsDepartment of Biomedical Sciences Center of Excellence for Neuroscience, Foster School of Medicine, Texas Tech Health Sciences Center, El Paso, Texas, USA.; Wassink-Ruiter JS

Subjects: Mutation*; DNA/DNA/DNA/*genetics ; Eye Diseases, Hereditary/Eye Diseases, Hereditary/Eye Diseases, Hereditary/*physiopathology Hyperopia, High

  • Source: Acta ophthalmologica [Acta Ophthalmol] 2014 May; Vol. 92 (3), pp. 276-81. Date of Electronic Publication: 2013 Jun 07.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101468102 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Developmental basis of nanophthalmos: MFRP Is required for both prenatal ocular growth and postnatal emmetropization.

  • Authors : Sundin OH; Wilmer Eye Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-92889, USA. ; Dharmaraj S

Subjects: Gene Deletion*; Hyperopia/Hyperopia/Hyperopia/*embryology ; Hyperopia/Hyperopia/Hyperopia/*physiopathology

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2008 Mar; Vol. 29 (1), pp. 1-9.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print Cited Medium: Internet ISSN: 1744-5094

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  • 1-10 ل  68 نتائج ل ""Microphthalmos""