Qazi ZA - Search Results

1

Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.

Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF. Riazuddin SA, et al. Among authors: qazi za. Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2264-70. doi: 10.1167/iovs.04-1280. Invest Ophthalmol Vis Sci. 2005. PMID: 15980210

2

Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani families.

Iqbal M, Naeem MA, Riazuddin SA, Ali S, Farooq T, Qazi ZA, Khan SN, Husnain T, Riazuddin S, Sieving PA, Hejtmancik JF, Riazuddin S. Iqbal M, et al. Among authors: qazi za. Arch Ophthalmol. 2011 Oct;129(10):1351-7. doi: 10.1001/archophthalmol.2011.267. Arch Ophthalmol. 2011. PMID: 21987678 Free PMC article.

3

Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families.

Khan SY, Ali S, Naeem MA, Khan SN, Husnain T, Butt NH, Qazi ZA, Akram J, Riazuddin S, Ayyagari R, Hejtmancik JF, Riazuddin SA. Khan SY, et al. Among authors: qazi za. Mol Vis. 2015 Aug 18;21:871-82. eCollection 2015. Mol Vis. 2015. PMID: 26321862 Free PMC article.

4

Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness.

Naeem MA, Gottsch AD, Ullah I, Khan SN, Husnain T, Butt NH, Qazi ZA, Akram J, Riazuddin S, Ayyagari R, Hejtmancik JF, Riazuddin SA. Naeem MA, et al. Among authors: qazi za. Mol Vis. 2015 Oct 31;21:1261-71. eCollection 2015. Mol Vis. 2015. PMID: 26628857 Free PMC article.

5

Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening.

Chen J, Wang Q, Cabrera PE, Zhong Z, Sun W, Jiao X, Chen Y, Govindarajan G, Naeem MA, Khan SN, Ali MH, Assir MZ, Rahman FU, Qazi ZA, Riazuddin S, Akram J, Riazuddin SA, Hejtmancik JF. Chen J, et al. Among authors: qazi za. Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2207-2217. doi: 10.1167/iovs.17-21469. Invest Ophthalmol Vis Sci. 2017. PMID: 28418495 Free PMC article.

6

Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1.

Yasmeen A, Riazuddin SA, Kaul H, Mohsin S, Khan M, Qazi ZA, Nasir IA, Zafar AU, Khan SN, Husnain T, Akram J, Hejtmancik JF, Riazuddin S. Yasmeen A, et al. Among authors: qazi za. Mol Vis. 2010 Apr 15;16:682-8. Mol Vis. 2010. PMID: 20405025 Free PMC article.

7

Ectopia lentis in a consanguineous pakistani family and a novel locus on chromosome 8q.

Kaul H, Riazuddin SA, Qazi ZA, Nasir IA, Zafar AU, Khan SN, Husnain T, Akram J, Hejtmancik JF, Riazuddin S. Kaul H, et al. Among authors: qazi za. Arch Ophthalmol. 2010 Aug;128(8):1046-9. doi: 10.1001/archophthalmol.2010.165. Arch Ophthalmol. 2010. PMID: 20697006 Free PMC article.

8

Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q.

Sabir N, Riazuddin SA, Butt T, Iqbal F, Nasir IA, Zafar AU, Qazi ZA, Butt NH, Khan SN, Husnain T, Hejtmancik JF, Riazuddin S. Sabir N, et al. Among authors: qazi za. Mol Vis. 2010 Dec 8;16:2634-8. Mol Vis. 2010. PMID: 21179239 Free PMC article.

9

Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p.

Sabir N, Riazuddin SA, Kaul H, Iqbal F, Nasir IA, Zafar AU, Qazi ZA, Butt NH, Khan SN, Husnain T, Hejtmancik JF, Riazuddin S. Sabir N, et al. Among authors: qazi za. Mol Vis. 2010 Dec 30;16:2911-5. Mol Vis. 2010. PMID: 21203409 Free PMC article.

10

Incidence of Rhegmatogenous Retinal Detachment (RRD) in a Tertiary Care Center of Pakistan.

Iqbal SM, Iqbal K, Shahid A, Iqbal F, Rahman FU, Tahir MJ, Qazi ZA, Raheem U, Butt JB, Ahmed M. Iqbal SM, et al. Among authors: qazi za. Cureus. 2022 May 17;14(5):e25092. doi: 10.7759/cureus.25092. eCollection 2022 May. Cureus. 2022. PMID: 35719781 Free PMC article.

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