Literature DB >> 9565065

Population-based assessment of childhood blindness in southern India.

L Dandona, J D Williams, B C Williams, G N Rao.   

Abstract

Entities:  

Mesh：

Year:  1998        PMID： 9565065

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  66 in total

1.  CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

Authors:  Fereshteh Chitsazian; Betsabeh Khoramian Tusi; Elahe Elahi; Heidar Amini Saroei; Mohammad H Sanati; Shahin Yazdani; Mohammad Pakravan; Navid Nilforooshan; Yadollah Eslami; Mohammad Ali Zare Mehrjerdi; Reza Zareei; Mahmood Jabbarvand; Ali Abdolahi; Ali R Lasheyee; Arash Etemadi; Behnaz Bayat; Mehdi Sadeghi; Mohammad M Banoei; Behnam Ghafarzadeh; Mohammad R Rohani; Akram Rismanchian; Yvonne Thorstenson; Mansoor Sarfarazi
Journal:  J Mol Diagn       Date:  2007-07       Impact factor: 5.568

2.  Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract.

Authors:  Surya Prakash G Ponnam; Kekunnaya Ramesha; Sushma Tejwani; Balasubramanya Ramamurthy; Chitra Kannabiran
Journal:  BMJ Case Rep       Date:  2009-06-30

3.  Changing pattern of childhood blindness in Maharashtra, India.

Authors:  P Gogate; M Deshpande; S Sudrik; S Taras; H Kishore; C Gilbert
Journal:  Br J Ophthalmol       Date:  2006-06-29       Impact factor: 4.638

4.  Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

Authors:  Meha Kabra; Wei Zhang; Sonika Rathi; Anil K Mandal; Sirisha Senthil; Goutham Pyatla; Muralidhar Ramappa; Seema Banerjee; Konegari Shekhar; Srinivas Marmamula; Asha L Mettla; Inderjeet Kaur; Rohit C Khanna; Hemant Khanna; Subhabrata Chakrabarti
Journal:  Hum Genet       Date:  2017-06-15       Impact factor: 4.132

5.  Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa.

Authors:  Kota Lalitha; Subhadra Jalali; Tejas Kadakia; Chitra Kannabiran
Journal:  J Genet       Date:  2002-08       Impact factor: 1.166

6.  A novel human CRYGD mutation in a juvenile autosomal dominant cataract.

Authors:  Mascarenhas Roshan; Pai H Vijaya; G Rao Lavanya; Prasada K Shama; S T Santhiya; Jochen Graw; P M Gopinath; K Satyamoorthy
Journal:  Mol Vis       Date:  2010-05-22       Impact factor: 2.367

7.  Mitochondrial DNA analysis in primary congenital glaucoma.

Authors:  Mukesh Tanwar; Tanuj Dada; Ramanjit Sihota; Rima Dada
Journal:  Mol Vis       Date:  2010-03-24       Impact factor: 2.367

8.  Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms.

Authors:  Sathiyavedu T Santhiya; Ganesan Senthil Kumar; Pridhvi Sudhakar; Navnit Gupta; Norman Klopp; Thomas Illig; Torben Söker; Marco Groth; Matthias Platzer; Puthiya M Gopinath; Jochen Graw
Journal:  Mol Vis       Date:  2010-09-10       Impact factor: 2.367

9.  Causes and temporal trends of blindness and severe visual impairment in children in schools for the blind in North India.

Authors:  J S Titiyal; N Pal; G V S Murthy; S K Gupta; R Tandon; R B Vajpayee; C E Gilbert
Journal:  Br J Ophthalmol       Date:  2003-08       Impact factor: 4.638

10.  Identification of four novel cytochrome P4501B1 mutations (p.I94X, p.H279D, p.Q340H, and p.K433K) in primary congenital glaucoma patients.

Authors:  Mukesh Tanwar; Tanuj Dada; Ramanjit Sihota; Rima Dada
Journal:  Mol Vis       Date:  2009-12-30       Impact factor: 2.367
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