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Academic Journal

Outcomes of Non-Penetrating Deep Sclerectomy for Primary Congenital Glaucoma Performed by Experienced versus Trainee Surgeons: A Cohort Study.

Subjects: CONGENITAL glaucoma; SURGEONS; COHORT analysisSAUDI Arabia

  • Source: Clinical Ophthalmology; Mar2023, Vol. 17, p897-906, 10p

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Academic Journal

CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia.

Subjects: *CONGENITAL glaucoma; *GENES; *ALLELESSAUDI Arabia

  • Source: BMC Medical Genetics. 2014, Vol. 15 Issue 1, p1-14. 14p.

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Academic Journal

Molecular Characterization of Newborn Glaucoma Including a Distinct Aniridic Phenotype.

Subjects: *CONGENITAL glaucoma; *NEONATAL diseases; *PHENOTYPESSAUDI Arabia

  • Source: Ophthalmic Genetics. Sep2011, Vol. 32 Issue 3, p138-142. 5p.

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Academic Journal

Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma.

  • Authors : Abu-Amero KK; a Ophthalmic Genetics Laboratory, Department of Ophthalmology , College of Medicine, King Saud University , Riyadh , Saudi Arabia .; b Department of Ophthalmology , College of Medicine, University of Florida , Jacksonville , FL , USA , and.

Subjects: Chromosome Deletion*; Abnormalities, Multiple/Abnormalities, Multiple/Abnormalities, Multiple/*genetics ; Chromosome Duplication/Chromosome Duplication/Chromosome Duplication/*genetics

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2016; Vol. 37 (1), pp. 98-101. Date of Electronic Publication: 2014 Jun 09.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Primary and secondary congenital glaucoma: baseline features from a registry at King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

  • Authors : Alanazi FF; King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.; Song JC

Subjects: Hospitals, Special* ; Intraocular Pressure* ; Registries*

  • Source: American journal of ophthalmology [Am J Ophthalmol] 2013 May; Vol. 155 (5), pp. 882-9. Date of Electronic Publication: 2013 Feb 06.Publisher: Elsevier Science Country of Publication: United States NLM ID: 0370500 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.

  • Authors : Abu-Amero KK; Ophthalmic Genetics Laboratory, Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia. ; Osman EA

Subjects: Aryl Hydrocarbon Hydroxylases/Aryl Hydrocarbon Hydroxylases/Aryl Hydrocarbon Hydroxylases/*genetics ; Eye Proteins/Eye Proteins/Eye Proteins/*genetics ; Glaucoma/Glaucoma/Glaucoma/*genetics

  • Source: Molecular vision [Mol Vis] 2011; Vol. 17, pp. 2911-9. Date of Electronic Publication: 2011 Nov 12.Publisher: Molecular Vision Country of Publication: United States NLM ID: 9605351 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).

Subjects: Mutation*; Cytochrome P-450 Enzyme System/Cytochrome P-450 Enzyme System/Cytochrome P-450 Enzyme System/*genetics ; Cytoskeletal Proteins/Cytoskeletal Proteins/Cytoskeletal Proteins/*genetics

  • Source: Journal of glaucoma [J Glaucoma] 2007 Jan; Vol. 16 (1), pp. 104-11.Publisher: Wolters Kluwer Health, Inc Country of Publication: United States NLM ID: 9300903 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humans.

  • Authors : Bidinost C; Health Research and Education Center, Washington State University Spokane, Spokane, Washington 99210-1495, USA.; Hernandez N

Subjects: Mutation*; Aryl Hydrocarbon Hydroxylases/Aryl Hydrocarbon Hydroxylases/Aryl Hydrocarbon Hydroxylases/*genetics ; Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/*genetics

  • Source: Investigative ophthalmology & visual science [Invest Ophthalmol Vis Sci] 2006 Apr; Vol. 47 (4), pp. 1486-90.Publisher: Association For Research In Vision And Ophthalmology (Arvo) Country of Publication: United States NLM ID: 7703701 Publication Model: Print Cited

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Academic Journal

Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia.

  • Authors : Bejjani BA; Department of Molecular Genetics, Baylor College of Medicine, Houston, TX 77030, USA.; Lewis RA

Subjects: Aryl Hydrocarbon Hydroxylases* ; Chromosomes, Human, Pair 2*; Cytochrome P-450 Enzyme System/Cytochrome P-450 Enzyme System/Cytochrome P-450 Enzyme System/*genetics

  • Source: American journal of human genetics [Am J Hum Genet] 1998 Feb; Vol. 62 (2), pp. 325-33.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print Cited Medium: Print ISSN: 0002-9297 (Print)

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Academic Journal

A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma.

  • Authors : Anderson KL; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.; Lewis RA

Subjects: Chromosomes, Human, Pair 1/Chromosomes, Human, Pair 1/Chromosomes, Human, Pair 1/*genetics ; Genetic Linkage/Genetic Linkage/Genetic Linkage/*genetics ; Glaucoma/Glaucoma/Glaucoma/*congenital

  • Source: Journal of glaucoma [J Glaucoma] 1996 Dec; Vol. 5 (6), pp. 416-21.Publisher: Wolters Kluwer Health, Inc Country of Publication: United States NLM ID: 9300903 Publication Model: Print Cited Medium: Print ISSN:

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  • 1-10 of  55 results for ""CONGENITAL glaucoma""