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Indian Pediatr. 2011 Jun;48(6):479-81. doi: 10.1007/s13312-011-0068-z.
DOOR syndrome: A case report and its embryological basis.
Santos M, Reis-Rego Â, Coutinho M, Almeida E Sousa C.
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James AW, Miranda SG, Culver K, Hall BD, Golabi M.
Am J Med Genet A. 2007 Dec 1;143A(23):2821-31. doi: 10.1002/ajmg.a.32054.
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Reducing the Emergency Department Revolving Door Syndrome for the Poor, Uninsured, and Chronically Ill Patient in Los Angeles: Process Improvement Recommendations from a County Health Program Evaluation.
Noulaheu SF.
Popul Health Manag. 2021 Jun;24(3):376-384. doi: 10.1089/pop.2020.0036. Epub 2020 Jul 16.
DOOR syndrome concomitant with non-convulsive status epilepticus and hyperintense cerebellar cortex on T2-weighted imaging.
Nomura T, Koyama N, Yokoyama M, Awaya A, Yokochi K.
Brain Dev. 2009 Jan;31(1):75-8. doi: 10.1016/j.braindev.2008.03.006. Epub 2008 Apr 28.
Unresolved questions regarding human hereditary deafness.
Rehman AU, Friedman TB, Griffith AJ.
Oral Dis. 2017 Jul;23(5):551-558. doi: 10.1111/odi.12516. Epub 2016 Jul 11.
Fryns syndrome without diaphragmatic hernia, DOOR syndrome or Fryns-like syndrome? Report on patients from Indian Ocean islands.
Alessandri JL, Cuillier F, Malan V, Brayer C, Grondard M, Jacquemot-Dekkak L, Kieffer-Traversier M, Pierre F, Laurain C, Samperiz S, Tiran-Rajaofera I, Ramful D.
Am J Med Genet A. 2014 Mar;164A(3):648-54. doi: 10.1002/ajmg.a.36323. Epub 2013 Dec 19.
DOOR syndrome: deficiency of E1 component of the 2-oxoglutarate dehydrogenase complex.
Surendran S, Michals-Matalon K, Krywawych S, Qazi QH, Tuchman R, Rady PL, Tyring SK, Matalon R.
Am J Med Genet. 2002 Dec 15;113(4):371-4. doi: 10.1002/ajmg.b.10804.
'Revolving door syndrome'.
Gordon A.
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