Haq Nawaz Khan - Search Results

Year	Number of Results
2016	1
2017	1
2018	4
2019	3
2020	1
2021	1
2022	3
2023	7
2024	4

1

Aminoacidopathies: Prevalence, Etiology, Screening, and Treatment Options.

Wasim M, Awan FR, Khan HN, Tawab A, Iqbal M, Ayesha H. Wasim M, et al. Among authors: khan hn. Biochem Genet. 2018 Apr;56(1-2):7-21. doi: 10.1007/s10528-017-9825-6. Epub 2017 Nov 1. Biochem Genet. 2018. PMID: 29094226 Review.

2

An Overview of Traditional and Novel Therapeutic Options for the Management of Phenylketonuria.

Wasim M, Awan FR, Khan HN, Ayesha H. Wasim M, et al. Among authors: khan hn. Crit Rev Eukaryot Gene Expr. 2018;28(2):177-185. doi: 10.1615/CritRevEukaryotGeneExpr.2018023073. Crit Rev Eukaryot Gene Expr. 2018. PMID: 30055544 Review.

3

Role of Leptin Deficiency, Inefficiency, and Leptin Receptors in Obesity.

Wasim M, Awan FR, Najam SS, Khan AR, Khan HN. Wasim M, et al. Among authors: khan hn. Biochem Genet. 2016 Oct;54(5):565-72. doi: 10.1007/s10528-016-9751-z. Epub 2016 Jun 16. Biochem Genet. 2016. PMID: 27313173 Review.

4

Need and Challenges in Establishing Newborn Screening Programs for Inherited Metabolic Disorders in Developing Countries.

Wasim M, Khan HN, Ayesha H, Awan FR. Wasim M, et al. Among authors: khan hn. Adv Biol (Weinh). 2023 Jul;7(7):e2200318. doi: 10.1002/adbi.202200318. Epub 2023 Apr 5. Adv Biol (Weinh). 2023. PMID: 37017505 Review.

5

Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Saadi SM, Cali E, Khalid LB, Yousaf H, Zafar G, Khan HN, Sher M, Vona B, Abdullah U, Malik NA, Klar J, Efthymiou S, Dahl N, Houlden H, Toft M, Baig SM, Fatima A, Iqbal Z. Saadi SM, et al. Among authors: khan hn. Genes (Basel). 2023 Jul 6;14(7):1404. doi: 10.3390/genes14071404. Genes (Basel). 2023. PMID: 37510308 Free PMC article.

6

Genetic Association of Beta-Myosin Heavy-Chain Gene (MYH7) with Cardiac Dysfunction.

Yousaf M, Khan WA, Shahzad K, Khan HN, Ali B, Hussain M, Awan FR, Mustafa H, Sheikh FN. Yousaf M, et al. Among authors: khan hn. Genes (Basel). 2022 Aug 29;13(9):1554. doi: 10.3390/genes13091554. Genes (Basel). 2022. PMID: 36140722 Free PMC article.

7

Adult GAMT deficiency: A literature review and report of two siblings.

Modi BP, Khan HN, van der Lee R, Wasim M, Haaxma CA, Richmond PA, Drögemöller B, Shah S, Salomons G, van der Kloet FM, Vaz FM, van der Crabben SN, Ross CJ, Wasserman WW, van Karnebeek CDM, Awan FR. Modi BP, et al. Among authors: khan hn. Mol Genet Metab Rep. 2021 Apr 26;27:100761. doi: 10.1016/j.ymgmr.2021.100761. eCollection 2021 Jun. Mol Genet Metab Rep. 2021. PMID: 33996490 Free PMC article.

8

High levels of blood glutamic acid and ornithine in children with intellectual disability.

Wasim M, Khan HN, Ayesha H, Tawab A, Habib FE, Asi MR, Iqbal M, Awan FR. Wasim M, et al. Among authors: khan hn. Int J Dev Disabil. 2020 Dec 21;68(5):609-614. doi: 10.1080/20473869.2020.1858520. eCollection 2022. Int J Dev Disabil. 2020. PMID: 36210897 Free PMC article.

9

Genetic association of vitamin D receptor gene with female infertility.

Ashraf M, Khan HN, Ibrahim R, Shahid M, Khan S, Fatima A, Ullah S, Rehman R. Ashraf M, et al. Among authors: khan hn. Nucleosides Nucleotides Nucleic Acids. 2024;43(2):116-133. doi: 10.1080/15257770.2023.2236167. Epub 2023 Jul 26. Nucleosides Nucleotides Nucleic Acids. 2024. PMID: 37496429

10

Development and application of low-cost T-ARMS-PCR assay for AGT and CYP11B1 gene polymorphisms.

Hussain M, Khan HN, Awan FR. Hussain M, et al. Among authors: khan hn. Mol Biol Rep. 2019 Feb;46(1):443-449. doi: 10.1007/s11033-018-4493-0. Epub 2018 Nov 26. Mol Biol Rep. 2019. PMID: 30478747

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