[1] |
Lance JW, Drummond PD, Gandevia SC,et al. Harlequin syndrome: the sudden onset of unilateral flushing and sweating[J] .J Neurol Neurosurg Psychiatry, 1988, 51(5):635-642.
doi: 10.1136/jnnp.51.5.635
URL
|
[2] |
Douvali T, Papageorgiou V, Gerochristou M, et al. Harlequin syndrome in a young girl: An opportunity to rethink the terminology[J]. Pediatr Dermatol, 2021, 38(4): 984-985.
doi: 10.1111/pde.14681
pmid: 34227168
|
[3] |
Elboukhari K, Baybay H, Elloudi S, et al. Idiopathic harlequin syndrome: A case report and literature review[J]. Pan Afr Med J, 2019, 33: 141.
doi: 10.11604/pamj.2019.33.141.18102
pmid: 31558939
|
[4] |
Schultz L, Mackarey A, Oh C, et al. Harlequin syndrome following microwave ablation in a child with a symptomatic paraspinal mass[J]. BMJ Case Rep, 2020, 13(8): e232700.
doi: 10.1136/bcr-2019-232700
URL
|
[5] |
Zhang ZQ, Zhang J, Chen YF. Harlequin syndrome[J]. J Eur Acad Dermatol Venereol, 2021, 35(9): e604-e605.
|
[6] |
Guilloton L, Demarquay G, Quesnel L, et al. Dysautonomic syndrome of the face with Harlequin sign and syndrome: Three new cases and a review of the literature[J]. Rev Neurol (Paris), 2013. 169(11):884-891.
doi: 10.1016/j.neurol.2013.01.628
URL
|
[7] |
Chen L, Zhou M. Must be sympathetic nervous system with unilateral facial flushing in harlequin syndrome[J]. Lancet, 2021, 397 (10271): 318.
doi: 10.1016/S0140-6736(21)00087-8
pmid: 33485456
|
[8] |
Kang JH, Shahzad Zafar M, Werner KE. Child Neurology: An infant with episodic facial flushing: A rare case and review of congenital harlequin syndrome[J]. Neurology, 2018, 91(6): 278-281.
doi: 10.1212/WNL.0000000000005949
pmid: 30082439
|
[9] |
Willaert WI, Scheltinga MR, Steenhuisen SF, et al. Harlequin syndrome: Two new cases and a management proposal[J]. Acta Neurol Belg, 2009, 109(3): 214-220.
pmid: 19902816
|
[10] |
Tascilar N, Tekin NS, Erdem Z, et al. Unnoticed dysautonomic syndrome of the face: Harlequin syndrome[J]. Auton Neurosci, 2007, 137 (1-2): 1-9.
doi: 10.1016/j.autneu.2007.05.004
URL
|
[11] |
Rovner MS, Redding AT, Wolf BJ, et al. Detection of subclinical Harlequin syndrome in pediatric patients[J]. Paediatr Anaesth, 2020, 30(5): 592-598.
doi: 10.1111/pan.13852
pmid: 32160375
|
[12] |
Tatebe M, Kawakami D. Harlequin syndrome after surgery for aortic dissection[J]. Intensive Care Med, 2021, 47(12): 1485-1486.
doi: 10.1007/s00134-021-06477-0
pmid: 34286361
|
[13] |
Redondo JM, Rivas M, Martín ML, et al. Harlequin syndrome as a rare complication after epidural anesthesia in an obstetric patient[J]. Minerva Anestesiol, 2018, 84(4): 524-526.
doi: 10.23736/S0375-9393.18.12310-8
pmid: 29343042
|
[14] |
Adams JS, Minzola DJ. Isolated Harlequin Syndrome Following Brachial Plexus Nerve Block via Interscalene Approach: A Case Report[J]. AANA J, 2018, 86(1): 56-58.
pmid: 31573494
|
[15] |
Lee DH, Seong JY, Yoon TM, et al. Harlequin syndrome and Horner syndrome after neck schwannoma excision in a pediatric patient: A case report[J]. Medicine (Baltimore), 2017, 96(45): e8548.
doi: 10.1097/MD.0000000000008548
URL
|
[16] |
Van Oosterhout WPJ. Patient with Cluster Headache and Harlequin Sign-Related or Not?[J]. Headache, 2020, 60(8): 1761-1766.
doi: 10.1111/head.13894
URL
|
[17] |
Kim HO, Kim JC, Chung BY, et al. Harlequin syndrome with petechiae caused by a pituitary adenoma[J]. J Eur Acad Dermatol Venereol, 2021, 35(9): e605-e607.
doi: 10.1111/jdv.17338
pmid: 33974308
|
[18] |
Beullens N, Tourlamain G, Vallaeys L, et al. Harlequin syndrome in a pediatric population: A case series[J]. Acta Neurol Belg, 2021, 121(3): 625-631.
doi: 10.1007/s13760-021-01593-6
pmid: 33515404
|
[19] |
Butragueño Laiseca L, Vázquez López M, Polo Arrondo A. Harlequin syndrome in a paediatric patient: A diagnostic challenge[J]. Neurologia (Engl Ed), 2018, 33(7): 478-480.
doi: 10.1016/j.nrl.2016.04.006
pmid: 27296496
|
[20] |
Boling B, Key C, Wainscott J, et al. Harlequin syndrome as a complication of epidural anesthesia[J]. Crit Care Nurse, 2014, 34(3): 57-61.
doi: 10.4037/ccn2014870
pmid: 24882829
|
[21] |
Algahtani H, Shirah B, Algahtani R, et al. Idiopathic harlequin syndrome manifesting during exercise: A case report and review of the literature[J]. Case Rep Med, 2017, 2017: 5342593.
|
[22] |
Mohindra A, Herd MK, Roszkowski N, et al. Concurrent Horner's and Harlequin syndromes[J]. Int J Oral Maxillofac Surg, 2015, 44(6): 710-712.
doi: 10.1016/j.ijom.2015.01.008
URL
|
[23] |
Bremner F, Smith S. Pupillographic findings in 39 consecutive cases of harlequin syndrome[J]. J Neuroophthalmol, 2008, 28(3): 171-177.
doi: 10.1097/WNO.0b013e318183c885
URL
|
[24] |
McKenna MC, Menon P, Smyth S, et al. Harlequin Syndrome in Acute Thalamic Hemorrhage[J]. J Stroke Cerebrovasc Dis, 2019, 28(9): e127-e128.
doi: 10.1016/j.jstrokecerebrovasdis.2019.06.037
|
[25] |
Lamotte G, Sandroni P, Cutsforth-Gregory JK, et al. Clinical presentation and autonomic profile in Ross syndrome[J]. J Neurol, 2021, 268(10): 3852-3860.
doi: 10.1007/s00415-021-10531-8
pmid: 33813643
|
[26] |
Reddy H, Fatah S, Gulve A, et al. Novel management of harlequin syndrome with stellate ganglion block[J]. Br J Dermatol, 2013, 169(4): 954-956.
doi: 10.1111/bjd.12561
pmid: 23909827
|
[27] |
Naharro-Fernández C, De Quintana-Sancho A, López-Sundh AE, et al. Successful treatment of idiopathic Harlequin Syndrome with oxybutynin and propranolol[J]. Australas J Dermatol, 2021, 62(4): 504-505.
doi: 10.1111/ajd.13665
pmid: 34314021
|
[28] |
Jain P, Arya R, Jaryal A, et al. Idiopathic harlequin syndrome: A pediatric case[J]. J Child Neurol, 2013, 28(4): 527-530.
doi: 10.1177/0883073812446484
pmid: 22638078
|