Ophthalmic Genetics,volume 31,issue 3  (09-2014)

Period of time: 2014年3期

Publisher: Informa Healthcare

Founded in: 1981

Total resources: 61

ISSN: 1381-6810

Subject: R77 Ophthalmology

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Ophthalmic Genetics,volume 31,issue 3

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eNOS gene polymorphism association with retinopathy in type 1 diabetes

By Bazzaz Javad Tavakkoly,Amoli Mahsa M.,Pravica Vera,Chandrasecaran Ramesh,Boulton Andrew J,Larijani Bagher,Hutchinson Ian V in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 103-107

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The relationship between ACE gene insertion/deletion polymorphism and diabetic retinopathy in Iranian patients with type 2 diabetes

By Nikzamir Abdolrahim,Rashidi Armin,Esteghamati Alireza,Nakhjavani Manouchehr,Golmohammadi Taghi,Khalilzadeh Omid in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 108-113

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Long-term 12 year follow-up of X-linked congenital retinoschisis

By Kjellström Sten,Vijayasarathy Camasamudram,Ponjavic Vesna,Sieving Paul A.,Andréasson Sten in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 114-125

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Leber’s hereditary optic neuropathy: Clinical and molecular profile of a Brazilian sample

By Maciel-Guerra Andréa Trevas,Zanchetta Luciene Maria,Amaral Fernandes Marcela Scabello,Andrade Paula Baloni,do Amor Divino Miranda Paulo Maurício,Sartorato Edi Lúcia in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 126-128

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Mutation screen of β-crystallin genes in 274 patients with age-related macular degeneration

By Sturgill Gwen M.,Bala Elisa,Yaniglos Stacia S.,Peachey Neal S.,Hagstrom Stephanie A. in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 129-134

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PITPNM3 is an uncommon cause of cone and cone-rod dystrophies

By Köhn Linda,Kohl Susanne,Bowne Sara J,Sullivan Lori S,Kellner Ulrich,Daiger Stephen P,Sandgren Ola,Golovleva Irina in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 139-140

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CDKN1C (p57KIP2) mRNA expression in human retinoblastomas

By Madhavan Jagadeesan,Mallikarjuna Kandalam,Vikas Khetan,George Ronnie,Bremner Rod,Kumaramanickavel Govindasamy in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 141-146

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Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy

By Abu-Amero Khaled K.,Hellani Ali,Salih Mustafa A.,Alorainy Ibrahim A.,Zidan Ghassan,Kern Kyle C.,Sicotte Nancy L.,Bosley Thomas M. in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 147-154

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Familial case of Blau syndrome associated with a CARD15/NOD2 mutation

By Villanueva-Mendoza Cristina,Arellanes-García Lourdes,Cubas-Lorenzo Victoria,Jimenez-Martinez Maria C.,Flores-Suárez Luis Felipe,Zenteno Juan Carlos in (2010)

Ophthalmic Genetics,volume 31,issue 3 , Vol. 31, Iss. 3, 2010-09 , pp. 155-158

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