Kaul H - Search Results

1

Fine mapping of chromosome 9 locus associated with congenital cataract.

Kaul H, Hussain S, Mustafa G, Naz S. Kaul H, et al. Int Ophthalmol. 2018 Jun;38(3):1187-1192. doi: 10.1007/s10792-017-0581-8. Epub 2017 Jun 5. Int Ophthalmol. 2018. PMID: 28585112

2

Genetic mapping of autosomal recessive microspherophakia to chromosome 14q24.3 in a consanguineous Pakistani family and screening of exon 36 of LTBP2 gene.

Shahzadi M, Firasat S, Kaul H, Afshan K, Afzal R, Naz S. Shahzadi M, et al. Among authors: kaul h. J Pak Med Assoc. 2020 Mar;70(3):515-518. doi: 10.5455/JPMA.302440. J Pak Med Assoc. 2020. PMID: 32207437

3

Homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene.

Shakil M, Ullah MI, Hussain S, Firasat S, Mahmood S, Kaul H. Shakil M, et al. Among authors: kaul h. Int J Ophthalmol. 2016 May 18;9(5):794-6. doi: 10.18240/ijo.2016.05.28. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27275442 Free PMC article. No abstract available.

4

Cytochrome 2C19 and paraoxonase-1 polymorphisms and clopidogrel resistance in ischemic heart disease patients.

Akram N, Mustafa G, Hanif AA, Tawwab S, Hussain S, Kaul H, Mohsin S. Akram N, et al. Among authors: kaul h. Per Med. 2019 Sep;16(5):379-386. doi: 10.2217/pme-2018-0030. Epub 2019 Oct 8. Per Med. 2019. PMID: 31591927

5

Association of Interleukin 10 (IL-10) Gene with Type 2 Diabetes Mellitus by Single Nucleotide Polymorphism of Its Promotor Region G/A 1082.

Naz S, Shafique N, Sharif S, Manzoor F, Saifi SZ, Firasat S, Kaul H. Naz S, et al. Among authors: kaul h. Crit Rev Eukaryot Gene Expr. 2020;30(4):285-289. doi: 10.1615/CritRevEukaryotGeneExpr.2020030714. Crit Rev Eukaryot Gene Expr. 2020. PMID: 32894658 Review.

6

SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families.

Firasat S, Dur-E-Shawar, Khan WA, Sughra U, Nousheen, Kaul H, Naz S, Noreen B, Gul R, Afshan K. Firasat S, et al. Among authors: kaul h. Mol Biol Rep. 2021 Nov;48(11):7467-7476. doi: 10.1007/s11033-021-06765-4. Epub 2021 Oct 12. Mol Biol Rep. 2021. PMID: 34637099 Clinical Trial.

7

Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan.

Iqbal A, Naz S, Kaul H, Sharif S, Khushbakht A, Naeem MA, Iqtedar M, Kaleem A, Firasat S, Manzoor F. Iqbal A, et al. Among authors: kaul h. PLoS One. 2022 Aug 29;17(8):e0273685. doi: 10.1371/journal.pone.0273685. eCollection 2022. PLoS One. 2022. PMID: 36037197 Free PMC article.

8

Prevalence of stromal corneal dystrophies in Lahore.

Naz S, Sharif S, Kaul H, Kaleem A, Tehseen A. Naz S, et al. Among authors: kaul h. J Pak Med Assoc. 2018 Apr;68(4):663-665. J Pak Med Assoc. 2018. PMID: 29808064

9

Determination of Serum Trace Elements (Zn, Cu, and Fe) in Pakistani Patients with Rheumatoid Arthritis.

Ullah Z, Ullah MI, Hussain S, Kaul H, Lone KP. Ullah Z, et al. Among authors: kaul h. Biol Trace Elem Res. 2017 Jan;175(1):10-16. doi: 10.1007/s12011-016-0746-8. Epub 2016 May 30. Biol Trace Elem Res. 2017. PMID: 27239678 Clinical Trial.

10

In silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma.

Firasat S, Kaul H, Ashfaq UA, Idrees S. Firasat S, et al. Among authors: kaul h. Int Ophthalmol. 2018 Apr;38(2):807-814. doi: 10.1007/s10792-017-0508-4. Epub 2017 Apr 6. Int Ophthalmol. 2018. PMID: 28386709

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