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

بواسطة Adkinson N Franklin, Hamilton Robert, Demetrides Susan, Levey Eric
منشور في 2007-12-01

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

بواسطة Danielsson, Aina J., Bartonek, Åsa, Levey, Eric, McHale, Kathleen, Sponseller, Paul, Saraste, Helena
منشور في 2007

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

بواسطة Gordon-Lipkin, Eliza, Cohen, Julie S., Srivastava, Siddharth, Soares, Bruno P., Levey, Eric, Fatemi, Ali
الحاوية / القاعدة J Child Neurol (2018)

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

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

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

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

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

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

A Diagnostic Approach for Cerebral Palsy in the Genomic Era

بواسطة Lee, Ryan W., Poretti, Andrea, Cohen, Julie S., Levey, Eric, Gwynn, Hilary, Johnston, Michael V., Hoon, Alexander H., Fatemi, Ali
الحاوية / القاعدة Neuromolecular Med (2014)

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

بواسطة 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
منشور في 2009

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

بواسطة 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
الحاوية / القاعدة Genet Med (2018)

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

بواسطة 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
منشور في 2010