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

von Adkinson N Franklin, Hamilton Robert, Demetrides Susan, Levey Eric
Veröffentlicht 2007-12-01

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

von Danielsson, Aina J., Bartonek, Åsa, Levey, Eric, McHale, Kathleen, Sponseller, Paul, Saraste, Helena
Veröffentlicht 2007

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

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

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

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

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

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

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

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

A Diagnostic Approach for Cerebral Palsy in the Genomic Era

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

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

von 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
Veröffentlicht 2009

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

von 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
Veröffentlicht in Genet Med (2018)

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

von 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
Veröffentlicht 2010