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Items: 1 to 20 of 88

1.

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics.

Markunas CA, Lock E, Soldano K, Cope H, Ding CK, Enterline DS, Grant G, Fuchs H, Ashley-Koch AE, Gregory SG.

BMC Med Genomics. 2014 Jun 25;7:39. doi: 10.1186/1755-8794-7-39.

2.

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.

3.

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
4.

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.

5.

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.

6.

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
7.

Clinical and radiological findings in Arnold Chiari malformation.

Khan AA, Bhatti SN, Khan G, Ahmed E, Aurangzeb A, Ali A, Khan A, Afzal S.

J Ayub Med Coll Abbottabad. 2010 Apr-Jun;22(2):75-8.

PMID:
21702272
8.

Posterior odontoid process angulation in pediatric Chiari I malformation: an MRI morphometric external validation study.

Ladner TR, Dewan MC, Day MA, Shannon CN, Tomycz L, Tulipan N, Wellons JC 3rd.

J Neurosurg Pediatr. 2015 Aug;16(2):138-45. doi: 10.3171/2015.1.PEDS14475. Epub 2015 May 22.

PMID:
26053869
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.

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.

11.

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
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.

[A complex of skull base and cervical spine anomalies and Chiari type I malformation].

Krupina NE, Beloded VM.

Zh Nevrol Psikhiatr Im S S Korsakova. 2002;102(8):3-7. Russian.

PMID:
12233255
14.
15.

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
16.

Cephalometric oropharynx and oral cavity analysis in Chiari malformation Type I: a retrospective case-control study.

Urbizu A, Ferré A, Poca MA, Rovira A, Sahuquillo J, Martin BA, Macaya A.

J Neurosurg. 2017 Feb;126(2):626-633. doi: 10.3171/2016.1.JNS151590. Epub 2016 May 6.

PMID:
27153161
17.

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
18.

Analysis of the volumes of the posterior cranial fossa, cerebellum, and herniated tonsils using the stereological methods in patients with Chiari type I malformation.

Vurdem ÜE, Acer N, Ertekin T, Savranlar A, Inci MF.

ScientificWorldJournal. 2012;2012:616934. doi: 10.1100/2012/616934. Epub 2012 May 2.

19.

Analysis of the posterior fossa in children with the Chiari 0 malformation.

Tubbs RS, Elton S, Grabb P, Dockery SE, Bartolucci AA, Oakes WJ.

Neurosurgery. 2001 May;48(5):1050-4; discussion 1054-5.

PMID:
11334271
20.

Expansion of Chiari I-associated syringomyelia after posterior-fossa decompression.

Gil Z, Rao S, Constantini S.

Childs Nerv Syst. 2000 Sep;16(9):555-8.

PMID:
11048628

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