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Combined TSC1 and LMX1B mutations in a single patient.
Khalifa O, Al-Sakati N, Al-Mane K, Balobaid A, Al-Hassnan ZN. Khalifa O, et al. Among authors: al mane k. Clin Dysmorphol. 2014 Apr;23(2):47-51. doi: 10.1097/MCD.0000000000000025. Clin Dysmorphol. 2014. PMID: 24477276
A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene.
Khalifa O, Imtiaz F, Allam R, Al-Hassnan Z, Al-Hemidan A, Al-Mane K, Abuharb G, Balobaid A, Sakati N, Hyland J, Al-Owain M. Khalifa O, et al. Among authors: al mane k. J Med Genet. 2012 Apr;49(4):246-8. doi: 10.1136/jmedgenet-2012-100783. J Med Genet. 2012. PMID: 22499343 No abstract available.
Extrinsic duodenal obstruction from anomalous congenital band.
Crankson SJ, Al-Mane KA, Al-Zaben A, Al-Dhafian A. Crankson SJ, et al. Among authors: al mane ka. Ann Saudi Med. 2000 Sep-Nov;20(5-6):443-4. doi: 10.5144/0256-4947.2000.443. Ann Saudi Med. 2000. PMID: 17264645 Free article. No abstract available.
CT findings in a child with reflux oesophagitis.
Crankson S, Al Salman MJ, Al Mane KA, Al Zaben AA. Crankson S, et al. Among authors: al mane ka. Trop Gastroenterol. 2004 Jan-Mar;25(1):47-8. Trop Gastroenterol. 2004. PMID: 15303475
Air emboli in the intracranial venous sinuses of neonates.
Al-Hathlol K, Al-Mane K, Al-Hathal M, Al-Tawil K, Abulaimoun B. Al-Hathlol K, et al. Among authors: al mane k. Am J Perinatol. 2002 Jan;19(1):55-8. doi: 10.1055/s-2002-20174. Am J Perinatol. 2002. PMID: 11857097
Intramuscular myxoma: a rare neck mass in a child.
Crankson SJ, Al Namshan M, Al Mane K, Bamefleh H. Crankson SJ, et al. Among authors: al mane k. Pediatr Radiol. 2002 Feb;32(2):120-2. doi: 10.1007/s00247-001-0603-5. Epub 2001 Dec 13. Pediatr Radiol. 2002. PMID: 11819080
16 results