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Items: 1 to 20 of 96

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.

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
3.

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
4.

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
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.

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
7.

Posterior fossa dimension and volume estimates in pediatric patients with Chiari I malformations.

Trigylidas T, Baronia B, Vassilyadi M, Ventureyra EC.

Childs Nerv Syst. 2008 Mar;24(3):329-36. Epub 2007 Jul 27.

PMID:
17657497
8.

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
9.

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
10.

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
11.

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
12.

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.

13.

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.

14.

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.

15.

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
16.

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.

17.

The road to the vertebral formula.

Mallo M, Vinagre T, Carapuço M.

Int J Dev Biol. 2009;53(8-10):1469-81. doi: 10.1387/ijdb.072276mm. Review.

18.

Morphometric comparison of foramen magnum in non-syndromic craniosynostosis patients with or without Chiari I malformation.

Leikola J, Haapamäki V, Karppinen A, Koljonen V, Hukki J, Valanne L, Koivikko M.

Acta Neurochir (Wien). 2012 Oct;154(10):1809-13. doi: 10.1007/s00701-012-1451-9. Epub 2012 Aug 7.

PMID:
22868492
19.

Positive association between ALDH1A2 and schizophrenia in the Chinese population.

Wan C, Shi Y, Zhao X, Tang W, Zhang M, Ji B, Zhu H, Xu Y, Li H, Feng G, He L.

Prog Neuropsychopharmacol Biol Psychiatry. 2009 Nov 13;33(8):1491-5. doi: 10.1016/j.pnpbp.2009.08.008. Epub 2009 Aug 22.

PMID:
19703508
20.

Cdx-Hox code controls competence for responding to Fgfs and retinoic acid in zebrafish neural tissue.

Shimizu T, Bae YK, Hibi M.

Development. 2006 Dec;133(23):4709-19. Epub 2006 Nov 1.

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