MeSH Review:
Language Development Disorders
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- Reversible brain creatine deficiency in two sisters with normal blood creatine level. Bianchi, M.C., Tosetti, M., Fornai, F., Alessandri', M.G., Cipriani, P., De Vito, G., Canapicchi, R. Ann. Neurol. (2000)
- A two-phased population epidemiological study of the safety of thimerosal-containing vaccines: a follow-up analysis. Geier, D.A., Geier, M.R. Med. Sci. Monit. (2005)
- Brain morphology in children with specific language impairment. Gauger, L.M., Lombardino, L.J., Leonard, C.M. J. Speech Lang. Hear. Res. (1997)
- History of in utero cocaine exposure in language-delayed children. Angelilli, M.L., Fischer, H., Delaney-Black, V., Rubinstein, M., Ager, J.W., Sokol, R.J. Clinical pediatrics. (1994)
- Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Buxbaum, J.D., Silverman, J.M., Smith, C.J., Kilifarski, M., Reichert, J., Hollander, E., Lawlor, B.A., Fitzgerald, M., Greenberg, D.A., Davis, K.L. Am. J. Hum. Genet. (2001)
- Predictors of outcome in perinatal arterial stroke: a population-based study. Lee, J., Croen, L.A., Lindan, C., Nash, K.B., Yoshida, C.K., Ferriero, D.M., Barkovich, A.J., Wu, Y.W. Ann. Neurol. (2005)
- Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay. Kwasnicka-Crawford, D.A., Carson, A.R., Roberts, W., Summers, A.M., Rehnström, K., Järvelä, I., Scherer, S.W. Genomics (2005)
- Central auditory processing disorder and ADHD. Jerome, L. Journal of the American Academy of Child and Adolescent Psychiatry. (2000)
- Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain. Miller, W.J., Skinner, J.A., Foss, G.S., Davies, K.E. Eur. J. Neurosci. (2000)
- A prospective evaluation of early language development in children with in utero cocaine exposure and in control subjects. Hurt, H., Malmud, E., Betancourt, L., Brodsky, N.L., Giannetta, J. J. Pediatr. (1997)
- Normal intrasylvian anatomical asymmetry in children with developmental language disorder. Preis, S., Jäncke, L., Schittler, P., Huang, Y., Steinmetz, H. Neuropsychologia. (1998)
- Phenobarbital side effects: hyperactivity with speech delay. Levenstein, D., Gutgesell, M.E., Percy, P. Pediatrics (1984)
- Urinary organic acid screening in children with developmental language delay. Michelson, M., Harel, S., Gutman, A., Lerman-Sagie, T. J. Inherit. Metab. Dis. (1999)
- Focal grey matter heterotopias in monozygotic twins with developmental language disorder. Preis, S., Engelbrecht, V., Huang, Y., Steinmetz, H. Eur. J. Pediatr. (1998)
- Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization. Zenger-Hain, J.L., Van Dyke, D.L., Wiktor, A., Walker, H., Feldman, G.L. Am. J. Med. Genet. (1993)
- Differential diagnosis and management of central auditory processing disorder and attention deficit hyperactivity disorder. Chermak, G.D., Hall, J.W., Musiek, F.E. Journal of the American Academy of Audiology. (1999)
- Clinical, electroencephalographic, and behavioral features of temporal lobe epilepsy in childhood. Franzon, R.C., Montenegro, M.A., Guimarães, C.A., Guerreiro, C.A., Cendes, F., Guerreiro, M.M. J. Child Neurol. (2004)
- The prevalence of the FMR1 and FMR2 mutations among preschool children with language delay. Mazzocco, M.M., Myers, G.F., Hamner, J.L., Panoscha, R., Shapiro, B.K., Reiss, A.L. J. Pediatr. (1998)
- GJB2 mutations and additional disabilities in a pediatric cochlear implant population. Wiley, S., Choo, D., Meinzen-Derr, J., Hilbert, L., Greinwald, J. Int. J. Pediatr. Otorhinolaryngol. (2006)
- D(+)-glyceric aciduria: etiology and clinical consequences. Bonham, J.R., Stephenson, T.J., Carpenter, K.H., Rattenbury, J.M., Cromby, C.H., Pollitt, R.J., Hull, D. Pediatr. Res. (1990)
- Special features of Graves' disease in early childhood. Segni, M., Leonardi, E., Mazzoncini, B., Pucarelli, I., Pasquino, A.M. Thyroid (1999)
- Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin. Mao, R., Jalal, S.M., Snow, K., Michels, V.V., Szabo, S.M., Babovic-Vuksanovic, D. Genet. Med. (2000)
- Comorbidity of central auditory processing disorder and attention-deficit hyperactivity disorder. Riccio, C.A., Hynd, G.W., Cohen, M.J., Hall, J., Molt, L. Journal of the American Academy of Child and Adolescent Psychiatry. (1994)
- Association of Chiari I malformation, mental retardation, speech delay, and epilepsy: a specific disorder? Grosso, S., Scattolini, R., Paolo, G., Di Bartolo, R.M., Morgese, G., Balestri, P. Neurosurgery (2001)
- Neurodevelopmental delay associated with nonconvulsive status epilepticus in a toddler. Shinawi, M., Shahar, E. J. Child Neurol. (2001)
- Neurocognitive outcome in pediatric liver transplant recipients. Krull, K., Fuchs, C., Yurk, H., Boone, P., Alonso, E. Pediatric transplantation. (2003)