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.
J Reconstr Microsurg., Jun;28(5):301-4 (2012)
Treatment practices for Chiari malformation type I with syringomyelia: results of a survey of the American Society of Pediatric Neurosurgeons.
J Neurosurg Pediatr., Nov;8(5):430-7 (2011)
Genetic basis of susceptibility to teratogen induced birth defects.
Am J Med Genet C Semin Med Genet., Aug;157(3):215-26 (2011)
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.
Pediatr Neurosurg., 46(6):415-6 (2010)
Defining the signs and symptoms of Chiari malformation type I with and without syringomyelia.
Neurol. Res., Apr;33(3):240-6 (2011)
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.
Pediatr Neurosurg., 45(6):478 (2009)
Hearing evaluation in pediatric patients treated at the hospital following head injury.
J Trauma Nurs., 16(3):169-78 (2009 Jul-Sep)
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.
Pediatr Neurosurg., 43(2):125-9 (2007)
Ventriculoperitoneal shunt failure causing myelopathy in a patient with bilateral jugular vein occlusion. Case report.
J Neurosurg Spine., Jan;6(1):60-3 (2007)
Chronic subdural hematoma of the neonate: report of two cases and literature review.
Pediatr Neurosurg., 43(1):25-8 (2007)
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.
Birth Defects Res. Part A Clin. Mol. Teratol., Jun;76(6):499-505 (2006)
Preoperative functional MR imaging localization of language and motor areas: effect on therapeutic decision making in patients with potentially resectable brain tumors.
Radiology., Sep;240(3):793-802 (2006)
Relationship of cine phase-contrast magnetic resonance imaging with outcome after decompression for Chiari I malformations.
Neurosurgery., Jul;59(1):140-6; discussion 140-6 (2006)