Current prevalence of latex sensitization in children with spina bifida with use of latex precautions

door Adkinson N Franklin, Hamilton Robert, Demetrides Susan, Levey Eric
Gepubliceerd in 2007-12-01

Associations between orthopaedic findings, ambulation and health-related quality of life in children with myelomeningocele

door Danielsson, Aina J., Bartonek, Åsa, Levey, Eric, McHale, Kathleen, Sponseller, Paul, Saraste, Helena
Gepubliceerd in 2007

ST3GAL5-related disorders: a deficiency in ganglioside metabolism and a genetic cause of intellectual disability and choreoathetosis.

door Gordon-Lipkin, Eliza, Cohen, Julie S., Srivastava, Siddharth, Soares, Bruno P., Levey, Eric, Fatemi, Ali
Gepubliceerd in J Child Neurol (2018)

Bowel and bladder continence among children with spina bifida: a retrospective study

door Zabel T Andrew, Lakshmanan Yeggepan, Slifer Keith, Rogers Valerie, Stashinko Elaine, Demetrides Susan, Campbell Michelle, Levey Eric
Gepubliceerd in 2007-12-01

Correlates of Depressive and Anxiety Symptoms in Young Adults with Spina Bifida *

door Bellin, Melissa H, Zabel, T. Andrew, Dicianno, Brad E., Levey, Eric, Garver, Kim, Linroth, Ronna, Braun, Patricia
Gepubliceerd in 2010

The Kennedy Krieger Independence Scales–Spina Bifida Version: A Measure of Executive Components of Self-Management

door Jacobson, Lisa A., Tarazi, Reem A., McCurdy, Mark D., Schultz, Scott, Levey, Eric, Mahone, E. Mark, Zabel, T. Andrew
Gepubliceerd in 2013

A Diagnostic Approach for Cerebral Palsy in the Genomic Era

door Lee, Ryan W., Poretti, Andrea, Cohen, Julie S., Levey, Eric, Gwynn, Hilary, Johnston, Michael V., Hoon, Alexander H., Fatemi, Ali
Gepubliceerd in Neuromolecular Med (2014)

Sensory and motor deficits in children with cerebral palsy born preterm correlate with diffusion tensor imaging abnormalities in thalamocortical pathways

door HOON, ALEXANDER H, STASHINKO, ELAINE E, NAGAE, LIDIA M, LIN, DORIS DM, KELLER, JENNIFER, BASTIAN, AMY, CAMPBELL, MICHELLE L, LEVEY, ERIC, MORI, SUSUMU, JOHNSTON, MICHAEL V
Gepubliceerd in 2009

In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristics

door Weiss, Karin, Kruszka, Paul, Guillen Sacoto, Maria J, Addissie, Yonit A, Hadley, Donald W, Hadsall, Casey K, Stokes, Bethany, Hu, Ping, Roessler, Erich, Solomon, Beth, Wiggs, Edythe, Thurm, Audrey, Hufnagel, Robert B, Zein, Wadih M, Hahn, Jin S, Stashinko, Elaine, Levey, Eric, Baldwin, Debbie, Clegg, Nancy J, Delgado, Mauricio R, Muenke, Maximilian
Gepubliceerd in Genet Med (2018)

Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

door Solomon, Benjamin D., Lacbawan, Felicitas, Mercier, Sandra, Clegg, Nancy J., Delgado, Mauricio R., Rosenbaum, Kenneth, Dubourg, Christèle, David, Véronique, Olney, Ann Haskins, Wehner, Lars-Erik, Hehr, Ute, Bale, Sherri, Paulussen, Aimee, Smeets, Hubert J., Hardisty, Emily, Tylki-Szymanska, Anna, Pronicka, Ewa, Clemens, Michelle, Mcpherson, Elizabeth, Hennekam, Raoul Cm, Hahn, Jin, Stashinko, Elaine, Levey, Eric, Wieczorek, Dagmar, Roeder, Elizabeth, Schell-Apacik, Chayim Can, Booth, Carol W., Thomas, Ronald L., Kenwrick, Sue, Keaton, Amelia, Balog, Joan Z., Hadley, Donald, Zhou, Nan, Long, Robert, Velez, Jorge I., Pineda-Alvarez, Daniel E., Odent, Sylvie, Roessler, Erich, Muenke, Maximilian
Gepubliceerd in 2010