DOOR syndrome.
Girish M, Mujawar N, Salodkar A.
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.
Int J Pediatr Otorhinolaryngol. 2019 Feb;117:57-60. doi: 10.1016/j.ijporl.2018.11.015. Epub 2018 Nov 14.
DOOR syndrome: additional case and literature review.
Bos CJ, Ippel PF, Beemer FA.
Clin Dysmorphol. 1994 Jan;3(1):15-20.
DOOR syndrome: clinical report, literature review and discussion of natural history.
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.
'Revolving door syndrome'.
Gordon A.
Elder Care. 1995 Aug-Sep;7(4):9-10, 12.
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.
The revolving door syndrome: the Chinese COPD patients' perspectives.
Yu DS, Lee DT, Woo J.
J Clin Nurs. 2007 Sep;16(9):1758-60. doi: 10.1111/j.1365-2702.2007.02089.x.
Further delineation of the DOOR syndrome.
Rajab A, Riaz A, Paul G, Al-Khusaibi S, Chalmers R, Patton MA.
Clin Dysmorphol. 2000 Oct;9(4):247-51. doi: 10.1097/00019605-200009040-00003.
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.
[Epilepsy syndromes associated with hearing loss].
Burd SG, Lebedeva AV, Rubleva YV, Pantina NV, Yurchenko AV, Bogomazova MA, Kovaleva II, Karchevskaya AE.
Zh Nevrol Psikhiatr Im S S Korsakova. 2023;123(1):28-33. doi: 10.17116/jnevro202312301128.
