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Page 1
Early Diagnosis of Classic Homocystinuria in Kuwait through Newborn Screening: A 6-Year Experience.
Int J Neonatal Screen. 2021 Aug 17;7(3):56. doi: 10.3390/ijns7030056.
Int J Neonatal Screen. 2021.
PMID: 34449519
Free PMC article.
Ethylmalonic encephalopathy-report of two cases.
Heberle LC, Al Tawari AA, Ramadan DG, Ibrahim JK.
Heberle LC, et al. Among authors: ramadan dg.
Brain Dev. 2006 Jun;28(5):329-31. doi: 10.1016/j.braindev.2005.10.005. Epub 2006 Jan 10.
Brain Dev. 2006.
PMID: 16376514
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Whole-exome sequencing gives additional benefits compared to candidate gene sequencing in the molecular diagnosis of children with growth hormone or IGF-1 insensitivity.
Shapiro L, Chatterjee S, Ramadan DG, Davies KM, Savage MO, Metherell LA, Storr HL.
Shapiro L, et al. Among authors: ramadan dg.
Eur J Endocrinol. 2017 Dec;177(6):485-501. doi: 10.1530/EJE-17-0453. Epub 2017 Sep 4.
Eur J Endocrinol. 2017.
PMID: 28870985
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Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p.
Hussain K, Bitner-Glindzicz M, Blaydon D, Lindley KJ, Thompson DA, Kriss T, Rajput K, Ramadan DG, Al-Mazidi Z, Cosgrove KE, Dunne MJ, Aynsley-Green A.
Hussain K, et al. Among authors: ramadan dg.
J Pediatr Endocrinol Metab. 2004 Dec;17(12):1613-21. doi: 10.1515/jpem.2004.17.12.1613.
J Pediatr Endocrinol Metab. 2004.
PMID: 15645695
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An early onset form of methylenetetrahydrofolate reductase deficiency: a report of a family from Kuwait.
Al Tawari AA, Ramadan DG, Neubauer D, Heberle LC, Al Awadi F.
Al Tawari AA, et al. Among authors: ramadan dg.
Brain Dev. 2002 Aug;24(5):304-9. doi: 10.1016/s0387-7604(02)00062-1.
Brain Dev. 2002.
PMID: 12142069
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