Khan MI - Search Results

1

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.

Azam M, Khan MI, Gal A, Hussain A, Shah ST, Khan MS, Sadeque A, Bokhari H, Collin RW, Orth U, van Genderen MM, den Hollander AI, Cremers FP, Qamar R. Azam M, et al. Among authors: khan ms, khan mi. Mol Vis. 2009 Dec 3;15:2526-34. Mol Vis. 2009. PMID: 19960070 Free PMC article.

2

A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.

Azam M, Collin RW, Khan MI, Shah ST, Qureshi N, Ajmal M, den Hollander AI, Qamar R, Cremers FP. Azam M, et al. Among authors: khan mi. Mol Vis. 2009 Sep 5;15:1788-93. Mol Vis. 2009. PMID: 19753316 Free PMC article.

3

Association of ABO blood groups with glaucoma in the Pakistani population.

Khan MI, Micheal S, Akhtar F, Naveed A, Ahmed A, Qamar R. Khan MI, et al. Can J Ophthalmol. 2009 Oct;44(5):582-6. doi: 10.3129/i09-104. Can J Ophthalmol. 2009. PMID: 19789596

4

MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma.

Micheal S, Qamar R, Akhtar F, Khan MI, Khan WA, Ahmed A. Micheal S, et al. Among authors: khan wa, khan mi. Mol Vis. 2009 Nov 9;15:2268-78. Mol Vis. 2009. PMID: 19936026 Free PMC article.

5

Association of tumor necrosis factor alpha gene polymorphism G-308A with pseudoexfoliative glaucoma in the Pakistani population.

Khan MI, Micheal S, Rana N, Akhtar F, den Hollander AI, Ahmed A, Qamar R. Khan MI, et al. Mol Vis. 2009 Dec 22;15:2861-7. Mol Vis. 2009. PMID: 20029655 Free PMC article.

6

Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts.

Ayub H, Khan MI, Micheal S, Akhtar F, Ajmal M, Shafique S, Ali SH, den Hollander AI, Ahmed A, Qamar R. Ayub H, et al. Among authors: khan mi. Mol Vis. 2010 Jan 11;16:18-25. Mol Vis. 2010. PMID: 20069064 Free PMC article.

7

Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia.

Azam M, Collin RW, Shah ST, Shah AA, Khan MI, Hussain A, Sadeque A, Strom TM, Thiadens AA, Roosing S, den Hollander AI, Cremers FP, Qamar R. Azam M, et al. Among authors: khan mi. Mol Vis. 2010 Apr 29;16:774-81. Mol Vis. 2010. PMID: 20454696 Free PMC article.

8

Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa.

Bandah-Rozenfeld D, Collin RW, Banin E, van den Born LI, Coene KL, Siemiatkowska AM, Zelinger L, Khan MI, Lefeber DJ, Erdinest I, Testa F, Simonelli F, Voesenek K, Blokland EA, Strom TM, Klaver CC, Qamar R, Banfi S, Cremers FP, Sharon D, den Hollander AI. Bandah-Rozenfeld D, et al. Among authors: khan mi. Am J Hum Genet. 2010 Aug 13;87(2):199-208. doi: 10.1016/j.ajhg.2010.07.004. Epub 2010 Jul 30. Am J Hum Genet. 2010. PMID: 20673862 Free PMC article.

9

The association of glutathione S-transferase GSTT1 and GSTM1 gene polymorphism with pseudoexfoliative glaucoma in a Pakistani population.

Khan MI, Micheal S, Akhtar F, Ahmed W, Ijaz B, Ahmed A, Qamar R. Khan MI, et al. Mol Vis. 2010 Oct 26;16:2146-52. Mol Vis. 2010. PMID: 21151336 Free PMC article.

10

Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa.

Khan MI, Collin RW, Arimadyo K, Micheal S, Azam M, Qureshi N, Faradz SM, den Hollander AI, Qamar R, Cremers FP. Khan MI, et al. Mol Vis. 2010 Dec 15;16:2753-9. Mol Vis. 2010. PMID: 21179430 Free PMC article.

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