Review of animal models of surgically induced spinal neural tube defects: Implications for fetal surgeryGEORGE, Timothy M; FUH, Eric.Pediatric neurosurgery. 2003, Vol 39, Num 2, pp 81-90, issn 1016-2291, 10 p.Article

Adult tethered cord syndrome in patients with postrepair myelomeningocele: an evidence-based outcome studyGEORGE, Timothy M; FAGAN, Lisa H.Journal of neurosurgery. Pediatrics. 2005, Vol 102, Num 2, pp 150-156, issn 1933-0707, 7 p.Article

The immunohistochemical profile of the myelomeningocele placode: Is the placode normal?GEORGE, Timothy M; CUMMINGS, Thomas J.Pediatric neurosurgery. 2003, Vol 39, Num 5, pp 234-239, issn 1016-2291, 6 p.Article

Comparison of revision rates following endoscopically versus nonendoscopically placed ventricular shunt catheters. CommentaryVILLAVICENCIO, Alan T; LEVEQUE, Jean-Christophe; MCGIRT, Matthew J et al.Surgical neurology. 2003, Vol 59, Num 5, pp 375-380, issn 0090-3019, 6 p.Article

Successful aqueductal plasty and stenting for tectal plate tumor after failed third ventriculostomy: A case report. CommentariesBULSARA, Ketan R; VILLAVICENCIO, Alan T; SHAH, Anand J et al.Surgical neurology. 2003, Vol 59, Num 1, pp 58-62, issn 0090-3019, 5 p.Article

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35STAMM, Demetra S; RAMPERSAUD, Evadnie; GILBERT, John R et al.Birth defects research. Clinical and molecular teratology. 2006, Vol 76, Num 6, pp 499-505, issn 1542-0752, 7 p.Conference Paper

T Locus shows no evidence for linkage disequilibrium or mutation in American caucasian neural tube defect familiesSPEER, Marcy C; MELVIN, Elizabeth C; GILBERT, John R et al.American journal of medical genetics. 2002, Vol 110, Num 3, pp 215-218, issn 0148-7299Article

Human neural tube defects : Developmental biology, epidemiology, and geneticsDETRAIT, Eric R; GEORGE, Timothy M; ETCHEVERS, Heather C et al.Neurotoxicology and teratology. 2005, Vol 27, Num 3, pp 515-524, issn 0892-0362, 10 p.Article

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defectsDEAK, Kristen L; BOYLES, Abee L; MCCLAY, David et al.Human genetics. 2005, Vol 117, Num 2-3, pp 133-142, issn 0340-6717, 10 p.Article

Treatment practices for Chiari malformation Type I with syringomyelia: results of a survey of the American Society of Pediatric Neurosurgeons: Clinical articleROCQUE, Brandon G; GEORGE, Timothy M; KESTLE, John et al.Journal of neurosurgery. Pediatrics. 2011, Vol 8, Num 5, pp 430-437, issn 1933-0707, 8 p.Article

Preoperative functional MR imaging localization of language and motor areas : Effect on therapeutic decision making in patients with potentially resectable brain tumorsPETRELLA, Jeffrey R; SHAH, Lubdha M; HARRIS, Katy M et al.Radiology. 2006, Vol 240, Num 3, pp 793-802, issn 0033-8419, 10 p.Article

TERC is not a major gene in human neural tube defectsBENZ, Lisa P; SWIFT, Frances E; GEORGE, Timothy M et al.Birth defects research. Clinical and molecular teratology. 2004, Vol 70, Num 8, pp 531-533, issn 1542-0752, 3 p.Article

The value of magnetic resonance imaging in the evaluation of fatty filum terminale. CommentariesBULSARA, Ketan R; ZOMORODI, Ali R; NAIDICH, Thomas P et al.Neurosurgery. 2004, Vol 54, Num 2, pp 375-380, issn 0148-396X, 6 p.Article

Comparison of total versus partial revision of initial ventriculoperitoneal shunt failuresMCGIRT, Matthew J; WELLONS, John C; NIMJEE, Shahid M et al.Pediatric neurosurgery. 2003, Vol 38, Num 1, pp 34-40, issn 1016-2291, 7 p.Article

Cerebrospinal fluid shunt survival and etiology of failures: A seven-year institutional experienceMCGIRT, Matthew J; LEVEQUE, Jean-Christophe; WELLONS, John C et al.Pediatric neurosurgery. 2002, Vol 36, Num 5, pp 248-255, issn 1016-2291Article

Capillary hemangioma of the fourth ventricle in an infantKARIKARI, Isaac O; SELZNICK, Lee A; CUMMINGS, Thomas J et al.Journal of neurosurgery. Pediatrics. 2006, Vol 104, Num 3, pp 188-191, issn 1933-0707, 4 p.Article

Relationship of cine phase-contrast magnetic resonance imaging with outcome after decompression for chiari I malformationsMCGIRT, Matthew J; NIMJEE, Shahid M; FUCHS, Herbert E et al.Neurosurgery. 2006, Vol 59, Num 1, pp 140-146, issn 0148-396X, 7 p.Article

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 15BOYLES, Abee L; ENTERLINE, David S; BENZEL, Edward et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 24, pp 2776-2785, issn 1552-4825, 10 p.Article

Correlation of cerebrospinal fluid flow dynamics and headache in Chiari I malformationMCGIRT, Matthew J; NIMJEE, Shahid M; FLOYD, James et al.Neurosurgery. 2005, Vol 56, Num 4, pp 716-721, issn 0148-396X, 6 p.Article

The immunohistochemical profile of the tethered filum terminaleGEORGE, Timothy M; BULSARA, Ketan R; CUMMINGS, Thomas J et al.Pediatric neurosurgery. 2003, Vol 39, Num 5, pp 227-233, issn 1016-2291, 7 p.Article

Clinical outcome differences for lipomyelomeningoceles, intraspinal lipomas, and lipomas of the filum terminaleBULSARA, Ketan R; ZOMORODI, Ali R; VILLAVICENCIO, Alan T et al.Neurosurgical review. 2001, Vol 24, Num 4, pp 192-194, issn 0344-5607Article

Antiepileptic Drugs and Pregnanc OutcomesWLODARCZYK, Bogdan J; PALACIOS, Ana M; GEORGE, Timothy M et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 8, pp 2071-2090, issn 1552-4825, 20 p.Article

Genetic Basis of Susceptibility to Teratogen Induced Birth DefectsWLODARCZYK, Bogdan J; PALACIOS, Ana M; CHAPA, Claudia J et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2011, Vol 157, Num 3, pp 215-226, issn 1552-4868, 12 p.Article

Ventriculoperitoneal shunt failure causing myelopathy in a patient with bilateral jugular vein occlusion : Case reportHUMPHRIES, William E; GROSSI, Peter M; LIETHE, Linda G et al.Journal of neurosurgery. Spine. 2007, Vol 6, Num 1, pp 60-63, issn 1547-5654, 4 p.Article

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2DEAK, Kristen L; DICKERSON, Margaret E; BASSUK, Alexander G et al.Birth defects research. Clinical and molecular teratology. 2005, Vol 73, Num 11, pp 868-875, issn 1542-0752, 8 p.Article