[1]王煜文 石长斌.Chiari畸形Ⅰ型临床表现的研究进展[J].中国临床神经外科杂志,2021,26(06):484-486.[doi:10.13798/j.issn.1009-153X.2021.06.026]
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Chiari畸形Ⅰ型临床表现的研究进展()
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《中国临床神经外科杂志》[ISSN:1009-153X/CN:42-1603/TN]

卷:
26
期数:
2021年06期
页码:
484-486
栏目:
综述
出版日期:
2021-06-25

文章信息/Info

文章编号:
1009-153X(2021)06-0484-03
作者:
王煜文 石长斌
作者单位:150081 哈尔滨,哈尔滨医科大学研究生院(王煜文);150001 哈尔滨,哈尔滨医科大学附属第一医院神经外科(石长斌)
关键词:
Chiari畸形I型临床表现弥散张量成像神经心理功能障碍
分类号:
R 742.8+2; R 651.1+1
DOI:
10.13798/j.issn.1009-153X.2021.06.026
文献标志码:
A

参考文献/References:

[1] Keser N, Kuskucu A, Is M, et al. Familial Chiari type 1: amolecular karyotyping study in a Turkish family and reviewof the literature [J]. World Neurosurg, 2019, 121: e852-e857.
[2] Markunas CA, Soldano K, Dunlap K, et al. Stratified wholegenome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates [J]. PLoS One, 2013, 8(4): e61521.
[3] Saletti V, Esposito S, Maccaro A, et al. Chiari I malformationin a child with PTEN hamartoma tumor syndrome: associa-tion or coincidence [J]. Eur J Med Genet, 2017, 60(5): 261-264.
[4] Han Y, Chen M, Wang H. Chiari I malformation in patients with RASopathies [J]. Childs Nerv Syst, 2021, 37(6): 1831-1836.
[5] Feghali J, Marinaro E, Xie Y, et al. Family history in Chiari malformation type I: presentation and outcome [J]. World Neurosurg, 2020, 142: e350-e356.
[6] Ravindra VM, Iyer RR, Awad AW, et al. Defining the role of the condylar-C2 sagittal vertical alignment in Chiari mal-formation type I [J]. J Neurosurg Pediatr, 2020. Online ahead of print. doi: 10.3171/2020.4.PEDS20113.
[7] Aitken LA, Lindan CE, Sidney S, et al. Chiari type I malfor-mation in a pediatric population [J]. Pediatr Neurol, 2009, 40(6): 449-454.
[8] Seaman SC, Dawson JD, Magnotta V, et al. Fourth ventricle enlargement in Chiari malformation type I [J]. World Neuro-surg, 2020, 133: e259-e266.
[9] Ozsoy KM, Oktay K, Cetinalp NE, et al. The role of cine flowmagnetic resonance imaging in patients with Chiari 0 mal-formation [J]. Turk Neurosurg, 2018, 28(2): 251-256.
[10] Hales PW, Smith V, Dhanoa-Hayre D, et al. Delineation of the visual pathway in paediatric optic pathway glioma patients using probabilistic tractography, and correlations with visual acuity [J]. Neuroimage Clin, 2018, 17: 541-548.
[11] Krishna V, Sammartino F, Yee P, et al. Diffusion tensorimaging assessment of microstructural brainstem integrity in Chiari malformation type I [J]. J Neurosurg, 2016, 125 (5): 1112-1119.
[12] Gok H, Naderi S. Prognostic value of craniovertebral junc-tion diffusion tensor imaging in patients with Chiari type 1 malformation [J]. Turk Neurosurg, 2020, 30(3): 400-406.
[13] Greenlee JD, Donovan KA, Hasan DM, et al. Chiari I mal-formation in the very young child: the spectrum of presenta-tions and experience in 31 children under age 6 years [J].Pediatrics, 2002, 110(6): 1212-1219.
[14] Massimi L, Della Pepa GM, Caldarelli M, et al. Abrupt cli-nical onset of Chiari type I/syringomyelia complex: clinical and physiopathological implications [J]. Neurosurg Rev,2012, 35(3): 321-329.
[15] Almotairi FS, Tisell M. Acute deterioration of adults with Chiari I malformation associated with extensive syrinx [J].Br J Neurosurg, 2020, 34(1): 13-17.
[16] Tubbs RS, Beckman J, Naftel RP, et al. Institutional experi-ence with 500 cases of surgically treated pediatric Chiari malformation type I [J]. J Neurosurg Pediatr, 2011, 7(3):248-256.
[17] Lacy M, Ellefson SE, Dedios-Stern S, et al. Parent-reported executive dysfunction in children and adolescents with Chiari malformation type 1 [J]. Pediatr Neurosurg,2016, 51(5): 236-243.
[18] Lacy M, Dedios-Stern S, Fredrickson S, et al. Prevalence of psychiatric diagnoses in pediatric Chiari malformation type 1 [J]. Pediatr Neurosurg, 2018, 53(6): 371-378.
[19] Allen PA, Houston JR, Pollock JW, et al. Task-specific and general cognitive effects in Chiari malformation type I [J].PLoS One, 2014, 9(4): e94844.
[20] Kumar M, Rathore RK, Srivastava A, et al. Correlation ofdiffusion tensor imaging metrics with neurocognitive func-tion in Chiari I malformation [J]. World Neurosurg, 2011, 76(1-2): 189-194.
[21] Riva D, Usilla A, Saletti V, et al. Can Chiari malformation negatively affect higher mental functioning in developmen-tal age [J]. Neurol Sci, 2011, 32 Suppl 3: S307-309.
[22] Almotairi FS, Hellst?rm P, Skoglund T, et al. Chiari I mal-formation-neuropsychological functions and quality of life[J]. Acta Neurochir (Wien), 2020, 162(7): 1575-1582.
[23] García M, Lázaro E, Amayra I, et al. Analysis of visuospatialabilities in Chiari malformation type I [J]. Cerebellum, 2020, 19(1): 6-15.
[24] García M, Lázaro E, López-Paz JF, et al. Cognitive func-tioning in Chiari malformation type I without posterior fossasurgery [J]. Cerebellum, 2018, 17(5): 564-574.
[25] García M, Amayra I, López-Paz JF, et al. Social cognition in Chiari malformation type I: a preliminary characterization[J]. Cerebellum, 2020, 19(3): 392-400.
[26] Elsamadicy AA, Koo AB, David WB, et al. Pre-operative headaches and obstructive hydrocephalus predict an extended length of stay following suboccipital decompres-sion for pediatric Chiari I malformation [J]. Childs Nerv Syst, 2021, 37(1): 91-99.
[27] Luciano MG, Batzdorf U, Kula RW, et al. Development of common data elements for use in Chiari malformation type I clinical research: an NIH/NINDS project [J]. Neurosurgery,2019, 85(6): 854-860.

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备注/Memo

备注/Memo:
通讯作者:石长斌,E-mail:changbinshi@hotmail.com
更新日期/Last Update: 2021-06-25