Výsledky vyhledávání - Taranath, Deepa

Case report: North Carolina macular dystrophy misdiagnosed as congenital ocular toxoplasmosis Autor Tandon, Moktika, Barnett, Christopher, Taranath, Deepa

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Macular Hypoplasia in Congenital Disorder of Glycosylation Type Ia Autor Wang, Bob Z., Siriwardana, Pradeep, Taranath, Deepa

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Orbital Subperiosteal Hematoma in the Newborn Causing Unilateral Proptosis: Ultrasound as First-Line Imaging Modality Autor Angkasa, Florencia, Mohammadi, Leila, Taranath, Deepa, Taranath, Ajay, Brecht, Marcus

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Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia Autor Dave, Alpana, Laurie, Kate, Staffieri, Sandra E., Taranath, Deepa, Mackey, David A., Mitchell, Paul, Wang, Jie Jin, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani

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Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract Autor Siggs, Owen M, Javadiyan, Shari, Sharma, Shiwani, Souzeau, Emmanuelle, Lower, Karen M, Taranath, Deepa A, Black, Jo, Pater, John, Willoughby, John G, Burdon, Kathryn P, Craig, Jamie E

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High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia Autor Javadiyan, Shari, Craig, Jamie E., Souzeau, Emmanuelle, Sharma, Shiwani, Lower, Karen M., Mackey, David A., Staffieri, Sandra E., Elder, James E., Taranath, Deepa, Straga, Tania, Black, Joanna, Pater, John, Casey, Theresa, Hewitt, Alex W., Burdon, Kathryn P.

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Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants Autor Souzeau, Emmanuelle, Siggs, Owen M, Zhou, Tiger, Galanopoulos, Anna, Hodson, Trevor, Taranath, Deepa, Mills, Richard A, Landers, John, Pater, John, Smith, James E, Elder, James E, Rait, Julian L, Giles, Paul, Phakey, Vivek, Staffieri, Sandra E, Kearns, Lisa S, Dubowsky, Andrew, Mackey, David A, Hewitt, Alex W, Ruddle, Jonathan B, Burdon, Kathryn P, Craig, Jamie E

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Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants Autor Souzeau, Emmanuelle, Siggs, Owen M, Zhou, Tiger, Galanopoulos, Anna, Hodson, Trevor, Taranath, Deepa, Mills, Richard A, Landers, John, Pater, John, Smith, James E, Elder, James E, Rait, Julian L, Giles, Paul, Phakey, Vivek, Staffieri, Sandra E, Kearns, Lisa S, Dubowsky, Andrew, Mackey, David A, Hewitt, Alex W, Ruddle, Jonathan B, Burdon, Kathryn P, Craig, Jamie E

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Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma Autor Siggs, Owen M., Souzeau, Emmanuelle, Pasutto, Francesca, Dubowsky, Andrew, Smith, James E. H., Taranath, Deepa, Pater, John, Rait, Julian L., Narita, Andrew, Mauri, Lucia, Del Longo, Alessandra, Reis, André, Chappell, Angela, Kearns, Lisa S., Staffieri, Sandra E., Elder, James E., Ruddle, Jonathan B., Hewitt, Alex W., Burdon, Kathryn P., Mackey, David A., Craig, Jamie E.

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