Antiepileptic drugs and pregnancy outcomes.
Am. J. Med. Genet. A., Aug;158A(8):2071-90 (2012)
The reliability and advantages of the sentinel vein as a microsurgical recipient vessel.
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Treatment practices for Chiari malformation type I with syringomyelia: results of a survey of the American Society of Pediatric Neurosurgeons.
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Genetic basis of susceptibility to teratogen induced birth defects.
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Commentary on 'quality of life and myelomeningocele: an ethical and evidence-based analysis of the Groningen Protocol' by Sean Barry, Pediatr Neurosurg 2010;46:409-414.
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Defining the signs and symptoms of Chiari malformation type I with and without syringomyelia.
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Polymorphisms of 5,10-Methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in SÃ©tif, Algeria. Concerning the article by Houcher et al., Pediatr Neurosurg 2009;45:472-477.
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Hearing evaluation in pediatric patients treated at the hospital following head injury.
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Few isolated neurons in hypothalamic hamartomas may cause gelastic seizures.
Pediatr Neurosurg., 45(3):225-9 (2009)
Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects.
Birth Defects Res. Part A Clin. Mol. Teratol., Oct;82(10):662-9 (2008)
Refinement of 2q and 7p loci in a large multiplex NTD family.
Birth Defects Res. Part A Clin. Mol. Teratol., Jun;82(6):441-52 (2008)
Primary cerebral ALK-1-positive anaplastic large cell lymphoma in a child. Case report and literature review.
Pediatr Neurosurg., 43(6):516-21 (2007)
Spinal capillary hemangioma in infants: report of two cases and review of the literature.
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Ventriculoperitoneal shunt failure causing myelopathy in a patient with bilateral jugular vein occlusion. Case report.
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Chronic subdural hematoma of the neonate: report of two cases and literature review.
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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.
Am. J. Med. Genet. A., Dec;140(24):2776-85 (2006)
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.
Environ. Health Perspect., Oct;114(10):1547-52 (2006)
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-q35.
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Preoperative functional MR imaging localization of language and motor areas: effect on therapeutic decision making in patients with potentially resectable brain tumors.
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Relationship of cine phase-contrast magnetic resonance imaging with outcome after decompression for Chiari I malformations.
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Capillary hemangioma of the fourth ventricle in an infant. Case report and review of the literature.
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Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.
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Adult tethered cord syndrome in patients with postrepair myelomeningocele: an evidence-based outcome study.
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Human neural tube defects: developmental biology, epidemiology, and genetics.
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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.
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Correlation of cerebrospinal fluid flow dynamics and headache in Chiari I malformation.
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Recurrence risks for neural tube defects in siblings of patients with lipomyelomeningocele.
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TERC is not a major gene in human neural tube defects.
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The pathology of extracranial scalp and skull masses in young children.
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The value of magnetic resonance imaging in the evaluation of fatty filum terminale.
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The immunohistochemical profile of the myelomeningocele placode: is the placode normal?
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The immunohistochemical profile of the tethered filum terminale.
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Avoiding complicated shunt systems by open fenestration of symptomatic fourth ventricular cysts associated with hydrocephalus.
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Intradural spinal teratoma: evidence for a dysembryogenic origin. Report of four cases.
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Postneurulation rapid brain growth represents a critical time for encephalocele formation: a chick model.
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Brainstem tethering in Dandy-Walker syndrome: a complication of cystoperitoneal shunting. Case report.
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Operative resection of 100 spinal lipomas in infants less than 1 year of age.
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Mechanisms of mutant genes in spina bifida: a review of implications from animal models.
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