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Page 1
CLRN1 mutations cause nonsyndromic retinitis pigmentosa.
Khan MI, Kersten FF, Azam M, Collin RW, Hussain A, Shah ST, Keunen JE, Kremer H, Cremers FP, Qamar R, den Hollander AI. Khan MI, et al. Among authors: shah st. Ophthalmology. 2011 Jul;118(7):1444-8. doi: 10.1016/j.ophtha.2010.10.047. Epub 2011 Feb 18. Ophthalmology. 2011. PMID: 21310491
Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosa.
Azam M, Collin RW, Malik A, Khan MI, Shah ST, Shah AA, Hussain A, Sadeque A, Arimadyo K, Ajmal M, Azam A, Qureshi N, Bokhari H, Strom TM, Cremers FP, Qamar R, den Hollander AI. Azam M, et al. Among authors: shah st, shah aa. Arch Ophthalmol. 2011 Oct;129(10):1377-8. doi: 10.1001/archophthalmol.2011.290. Arch Ophthalmol. 2011. PMID: 21987686 No abstract available.
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.
Shafique S, Siddiqi S, Schraders M, Oostrik J, Ayub H, Bilal A, Ajmal M, Seco CZ, Strom TM, Mansoor A, Mazhar K, Shah ST, Hussain A, Azam M, Kremer H, Qamar R. Shafique S, et al. Among authors: shah st. PLoS One. 2014 Jun 20;9(6):e100146. doi: 10.1371/journal.pone.0100146. eCollection 2014. PLoS One. 2014. PMID: 24949729 Free PMC article.
NeoVault: empowering neonatal research through a neonate data hub.
Pigueiras-Del-Real J, Ruiz-Zafra A, Benavente-Fernández I, Lubián-López SP, Shah SAH, Shah STH, Gontard LC. Pigueiras-Del-Real J, et al. Among authors: shah sth. BMC Pediatr. 2024 Nov 30;24(1):787. doi: 10.1186/s12887-024-05276-y. BMC Pediatr. 2024. PMID: 39614275 Free PMC article.
Data-driven classification and explainable-AI in the field of lung imaging.
Shah STH, Shah SAH, Khan II, Imran A, Shah SBH, Mehmood A, Qureshi SA, Raza M, Di Terlizzi A, Cavaglià M, Deriu MA. Shah STH, et al. Front Big Data. 2024 Sep 19;7:1393758. doi: 10.3389/fdata.2024.1393758. eCollection 2024. Front Big Data. 2024. PMID: 39364222 Free PMC article. Review.
133 results