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Items: 1 to 20 of 97

1.

Chiari malformation type I: a case-control association study of 58 developmental genes.

Urbizu A, Toma C, Poca MA, Sahuquillo J, Cuenca-León E, Cormand B, Macaya A.

PLoS One. 2013;8(2):e57241. doi: 10.1371/journal.pone.0057241. Epub 2013 Feb 21.

2.

Incidence of basioccipital hypoplasia in Chiari malformation type I: comparative morphometric study of the posterior cranial fossa. Clinical article.

Noudel R, Jovenin N, Eap C, Scherpereel B, Pierot L, Rousseaux P.

J Neurosurg. 2009 Nov;111(5):1046-52. doi: 10.3171/2009.2.JNS08284.

PMID:
19463049
3.

MRI-based morphometric analysis of posterior cranial fossa in the diagnosis of chiari malformation type I.

Urbizu A, Poca MA, Vidal X, Rovira A, Sahuquillo J, Macaya A.

J Neuroimaging. 2014 May-Jun;24(3):250-6. doi: 10.1111/jon.12007. Epub 2013 Jan 16.

PMID:
23324118
4.

Posterior cranial fossa morphometry in symptomatic adult Chiari I malformation patients: comparative clinical and anatomical study.

Dagtekin A, Avci E, Kara E, Uzmansel D, Dagtekin O, Koseoglu A, Talas D, Bagdatoglu C.

Clin Neurol Neurosurg. 2011 Jun;113(5):399-403. doi: 10.1016/j.clineuro.2010.12.020. Epub 2011 Feb 18.

PMID:
21333437
5.

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation.

Markunas CA, Enterline DS, Dunlap K, Soldano K, Cope H, Stajich J, Grant G, Fuchs H, Gregory SG, Ashley-Koch AE.

Ann Hum Genet. 2014 Jan;78(1):1-12. doi: 10.1111/ahg.12041. Epub 2013 Oct 6.

6.

Zebrafish foxc1a plays a crucial role in early somitogenesis by restricting the expression of aldh1a2 directly.

Li J, Yue Y, Dong X, Jia W, Li K, Liang D, Dong Z, Wang X, Nan X, Zhang Q, Zhao Q.

J Biol Chem. 2015 Apr 17;290(16):10216-28. doi: 10.1074/jbc.M114.612572. Epub 2015 Feb 27.

7.

Pathogenesis of Chiari malformation: a morphometric study of the posterior cranial fossa.

Nishikawa M, Sakamoto H, Hakuba A, Nakanishi N, Inoue Y.

J Neurosurg. 1997 Jan;86(1):40-7.

PMID:
8988080
8.

Magnetic resonance imaging measures of posterior cranial fossa morphology and cerebrospinal fluid physiology in Chiari malformation type I.

Alperin N, Loftus JR, Oliu CJ, Bagci AM, Lee SH, Ertl-Wagner B, Green B, Sekula R.

Neurosurgery. 2014 Nov;75(5):515-22; discussion 522. doi: 10.1227/NEU.0000000000000507.

9.

Chiari type I malformations in adults: a morphometric analysis of the posterior cranial fossa.

Aydin S, Hanimoglu H, Tanriverdi T, Yentur E, Kaynar MY.

Surg Neurol. 2005 Sep;64(3):237-41; discussion 241.

PMID:
16099255
10.

Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial development.

Merello E, Tattini L, Magi A, Accogli A, Piatelli G, Pavanello M, Tortora D, Cama A, Kibar Z, Capra V, De Marco P.

Eur J Hum Genet. 2017 Aug;25(8):952-959. doi: 10.1038/ejhg.2017.71. Epub 2017 May 17.

PMID:
28513615
11.

Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients.

Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, Speer MC.

Neurosurgery. 1999 May;44(5):1005-17.

PMID:
10232534
12.

Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.

Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, Benzel E, Ellenbogen R, Green BA, Kula R, Menezes A, Mueller D, Oro' JJ, Iskandar BJ, George TM, Milhorat TH, Speer MC.

Am J Med Genet A. 2006 Dec 15;140(24):2776-85.

PMID:
17103432
13.

Automated posterior cranial fossa volumetry by MRI: applications to Chiari malformation type I.

Bagci AM, Lee SH, Nagornaya N, Green BA, Alperin N.

AJNR Am J Neuroradiol. 2013 Sep;34(9):1758-63. doi: 10.3174/ajnr.A3435. Epub 2013 Mar 14.

14.

Volumetric analysis of the posterior cranial fossa in a family with four generations of the Chiari malformation Type I.

Tubbs RS, Hill M, Loukas M, Shoja MM, Oakes WJ.

J Neurosurg Pediatr. 2008 Jan;1(1):21-4. doi: 10.3171/PED-08/01/021.

PMID:
18352798
15.

[Genetic analysis of posterior cranial fossa morphology in families of Chiari malformation type Ⅰ].

Yuan XX, Li Y, Sha SF, Sun WX, Qiu Y, Liu Z, Zhu WG, Zhu ZZ.

Zhonghua Yi Xue Za Zhi. 2017 Apr 18;97(15):1140-1144. doi: 10.3760/cma.j.issn.0376-2491.2017.15.006. Chinese.

PMID:
28427119
16.

Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management.

Milhorat TH, Nishikawa M, Kula RW, Dlugacz YD.

Acta Neurochir (Wien). 2010 Jul;152(7):1117-27. doi: 10.1007/s00701-010-0636-3. Epub 2010 May 4.

17.

Cdx1 and Cdx2 have overlapping functions in anteroposterior patterning and posterior axis elongation.

van den Akker E, Forlani S, Chawengsaksophak K, de Graaff W, Beck F, Meyer BI, Deschamps J.

Development. 2002 May;129(9):2181-93.

18.

Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

Markunas CA, Soldano K, Dunlap K, Cope H, Asiimwe E, Stajich J, Enterline D, Grant G, Fuchs H, Gregory SG, Ashley-Koch AE.

PLoS One. 2013 Apr 19;8(4):e61521. doi: 10.1371/journal.pone.0061521. Print 2013.

19.

Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation.

Lock EF, Soldano KL, Garrett ME, Cope H, Markunas CA, Fuchs H, Grant G, Dunson DB, Gregory SG, Ashley-Koch AE.

BMC Genomics. 2015 Jan 22;16:11. doi: 10.1186/s12864-014-1211-8.

20.

Posterior fossa morphometry in symptomatic pediatric and adult Chiari I malformation.

Furtado SV, Reddy K, Hegde AS.

J Clin Neurosci. 2009 Nov;16(11):1449-54. doi: 10.1016/j.jocn.2009.04.005. Epub 2009 Sep 6.

PMID:
19736012

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