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

Por Adkinson N Franklin, Hamilton Robert, Demetrides Susan, Levey Eric
Publicado em 2007-12-01

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

Por Danielsson, Aina J., Bartonek, Åsa, Levey, Eric, McHale, Kathleen, Sponseller, Paul, Saraste, Helena
Publicado em 2007

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

Por Gordon-Lipkin, Eliza, Cohen, Julie S., Srivastava, Siddharth, Soares, Bruno P., Levey, Eric, Fatemi, Ali
Publicado no J Child Neurol (2018)

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

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

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

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

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

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

A Diagnostic Approach for Cerebral Palsy in the Genomic Era

Por Lee, Ryan W., Poretti, Andrea, Cohen, Julie S., Levey, Eric, Gwynn, Hilary, Johnston, Michael V., Hoon, Alexander H., Fatemi, Ali
Publicado no Neuromolecular Med (2014)

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

Por 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
Publicado em 2009

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

Por 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
Publicado no Genet Med (2018)

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

Por 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
Publicado em 2010