Wasim M - Search Results

1

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

Wasim M, Awan FR, Khan HN, Tawab A, Iqbal M, Ayesha H. Wasim M, et al. 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

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

Wasim M, Awan FR, Najam SS, Khan AR, Khan HN. Wasim M, et al. 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.

3

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. Crit Rev Eukaryot Gene Expr. 2018;28(2):177-185. doi: 10.1615/CritRevEukaryotGeneExpr.2018023073. Crit Rev Eukaryot Gene Expr. 2018. PMID: 30055544 Review.

4

Molecular genetic diagnosis of Wilson disease by ARMS-PCR in a Pakistani family.

Khan HN, Wasim M, Ayesha H, Awan FR. Khan HN, et al. Among authors: wasim m. Mol Biol Rep. 2018 Dec;45(6):2585-2591. doi: 10.1007/s11033-018-4426-y. Epub 2018 Nov 13. Mol Biol Rep. 2018. PMID: 30426382

5

Biochemical Screening of Intellectually Disabled Patients: A Stepping Stone to Initiate a Newborn Screening Program in Pakistan.

Wasim M, Khan HN, Ayesha H, Goorden SMI, Vaz FM, van Karnebeek CDM, Awan FR. Wasim M, et al. Front Neurol. 2019 Jul 17;10:762. doi: 10.3389/fneur.2019.00762. eCollection 2019. Front Neurol. 2019. PMID: 31379716 Free PMC article.

6

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: wasim m. 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.

7

Biochemical screening of intellectually disabled and healthy children in Punjab, Pakistan: differences in liver function test and lipid profiles.

Wasim M, Khan HN, Ayesha H, Awan FR. Wasim M, et al. Int J Dev Disabil. 2019 Jan 15;66(3):190-195. doi: 10.1080/20473869.2018.1533084. Int J Dev Disabil. 2019. PMID: 34141381 Free PMC article.

8

Identification of three novel pathogenic mutations in cystathionine beta-synthase gene of Pakistani intellectually disabled patients.

Wasim M, Khan HN, Ayesha H, Iqbal M, Tawab A, Irfan M, Kanhai W, Goorden SMI, Stroomer L, Salomons G, Vaz FM, Karnebeek CDMV, Awan FR. Wasim M, et al. J Pediatr Endocrinol Metab. 2021 Dec 14;35(3):325-332. doi: 10.1515/jpem-2021-0508. Print 2022 Mar 28. J Pediatr Endocrinol Metab. 2021. PMID: 34905667

9

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. 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.

10

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. Adv Biol (Weinh). 2023 Jul;7(7):e2200318. doi: 10.1002/adbi.202200318. Epub 2023 Apr 5. Adv Biol (Weinh). 2023. PMID: 37017505 Review.

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