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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2009 4
2010 2
2011 2
2012 8
2013 12
2014 10
2015 2
2016 1
2017 2
2018 2
2019 2
2020 5
2021 6
2022 9
2023 11
2024 4

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75 results

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Page 1
The potential of stem cell therapy to tackle visual impairment.
Hassan M, Rajput SK, Salma J, Kirmani S, F Damji K. Hassan M, et al. Among authors: kirmani s. J Pak Med Assoc. 2023 Feb;73(Suppl 1)(2):S79-S88. doi: 10.47391/JPMA.AKUS-13. J Pak Med Assoc. 2023. PMID: 36788396 Free article. Review.
Position paper: Challenges and specific strategies for constitutional mismatch repair deficiency syndrome in low-resource settings.
Kebudi R, Amayiri N, Abedalthagafi M, Rana AN, Kirmani S, Musthaq N, Lamki ZA, Houdzi JE, Yazici H, El-Naggar S, Edwards M, Bianchi VJ, Durno C, Tabori U, Bouffet E; International RRD Consortium on Low-Resource Settings Panel. Kebudi R, et al. Among authors: kirmani s. Pediatr Blood Cancer. 2020 Aug;67(8):e28309. doi: 10.1002/pbc.28309. Epub 2020 May 30. Pediatr Blood Cancer. 2020. PMID: 32472748 Review.
MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study.
Ansar Z, Nasir A, Moatter T, Khan S, Kirmani S, Ibrahim S, Imam K, Ather A, Samreen A, Hasan Z. Ansar Z, et al. Among authors: kirmani s. Genet Test Mol Biomarkers. 2019 Jul;23(7):468-472. doi: 10.1089/gtmb.2018.0262. Epub 2019 May 31. Genet Test Mol Biomarkers. 2019. PMID: 31157985 Review.
PIGG variant pathogenicity assessment reveals characteristic features within 19 families.
Tremblay-Laganière C, Maroofian R, Nguyen TTM, Karimiani EG, Kirmani S, Akbar F, Ibrahim S, Afroze B, Doosti M, Ashrafzadeh F, Babaei M, Efthymiou S, Christoforou M, Sultan T, Ladda RL, McLaughlin HM, Truty R, Mahida S, Cohen JS, Baranano K, Ismail FY, Patel MS, Lehman A, Edmondson AC, Nagy A, Walker MA, Mercimek-Andrews S, Maki Y, Sachdev R, Macintosh R, Palmer EE, Mancini GMS, Barakat TS, Steinfeld R, Rüsch CT, Stettner GM, Wagner M, Wortmann SB, Kini U, Brady AF, Stals KL, Ismayilova N, Ellard S, Bernardo D, Nugent K, McLean SD, Antonarakis SE, Houlden H, Kinoshita T, Campeau PM, Murakami Y. Tremblay-Laganière C, et al. Among authors: kirmani s. Genet Med. 2021 Oct;23(10):1873-1881. doi: 10.1038/s41436-021-01215-9. Epub 2021 Jun 10. Genet Med. 2021. PMID: 34113002 Free PMC article.
Wolcott-Rallison syndrome: a case series of three patients.
Memon F, Arif M, Kirmani S, Humayun K. Memon F, et al. Among authors: kirmani s. Pediatr Endocrinol Diabetes Metab. 2022;28(3):238-240. doi: 10.5114/pedm.2022.118325. Pediatr Endocrinol Diabetes Metab. 2022. PMID: 36106422 Free PMC article.
75 results