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WGC-2021

9.1.4 Other (20)

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Display all abstracts in classification 9.1.4 Other

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92529 Clinical spectrum and treatment outcomes of patients with nanophthalmos
Rajendrababu S
Eye 2021; 35: 825-830
92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Koenighofer M
Experimental Eye Research 2021; 205: 108497
92461 Congenital Microcoria: Clinical Features and Molecular Genetics
Angée C
Genes 2021; 12:
92694 Clinical and Histopathological Features of Congenital Fibrovascular Pupillary Membranes in a Chinese Case Series
Liang T; Liang T
Journal of Pediatric Ophthalmology & Strabismus 2021; 58: 105-111
92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Parzefall T
Experimental Eye Research 2021; 205: 108497
92461 Congenital Microcoria: Clinical Features and Molecular Genetics
Nedelec B
Genes 2021; 12:
92529 Clinical spectrum and treatment outcomes of patients with nanophthalmos
Shroff S
Eye 2021; 35: 825-830
92694 Clinical and Histopathological Features of Congenital Fibrovascular Pupillary Membranes in a Chinese Case Series
Zhang C
Journal of Pediatric Ophthalmology & Strabismus 2021; 58: 105-111
92461 Congenital Microcoria: Clinical Features and Molecular Genetics
Erjavec E
Genes 2021; 12:
92694 Clinical and Histopathological Features of Congenital Fibrovascular Pupillary Membranes in a Chinese Case Series
Fu L
Journal of Pediatric Ophthalmology & Strabismus 2021; 58: 105-111
92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Frohne A
Experimental Eye Research 2021; 205: 108497
92529 Clinical spectrum and treatment outcomes of patients with nanophthalmos
Uduman MS; Babu N
Eye 2021; 35: 825-830
92461 Congenital Microcoria: Clinical Features and Molecular Genetics
Rozet JM
Genes 2021; 12:
92694 Clinical and Histopathological Features of Congenital Fibrovascular Pupillary Membranes in a Chinese Case Series
Hu M
Journal of Pediatric Ophthalmology & Strabismus 2021; 58: 105-111
92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Frei E
Experimental Eye Research 2021; 205: 108497
92694 Clinical and Histopathological Features of Congenital Fibrovascular Pupillary Membranes in a Chinese Case Series
Zhang L
Journal of Pediatric Ophthalmology & Strabismus 2021; 58: 105-111
92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Waldstein SM
Experimental Eye Research 2021; 205: 108497
92461 Congenital Microcoria: Clinical Features and Molecular Genetics
Fares Taie L
Genes 2021; 12:
92694 Clinical and Histopathological Features of Congenital Fibrovascular Pupillary Membranes in a Chinese Case Series
Li L
Journal of Pediatric Ophthalmology & Strabismus 2021; 58: 105-111
92558 A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuity
Mitulovic G; Schoefer C; Frei K; Lucas T
Experimental Eye Research 2021; 205: 108497

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WGC-2021