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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
MeSH Review

Language Development Disorders

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Disease relevance of Language Development Disorders


Psychiatry related information on Language Development Disorders


High impact information on Language Development Disorders

  • Because decreasing sample heterogeneity would increase the power to identify genes, the effect on evidence for linkage of restricting a sample of autism-affected relative pairs to those with delayed onset (at age >36 mo) of phrase speech (PSD, for phrase speech delay) was studied [8].
  • Abnormal outcomes included CP (58%), epilepsy (39%), language delay (25%), and behavioral abnormalities (22%) [9].
  • Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay [10].
  • Central auditory processing disorder and ADHD [11].
  • FRAXE individuals have been shown to exhibit learning deficits, including speech delay, reading and writing problems [12].

Chemical compound and disease context of Language Development Disorders


Biological context of Language Development Disorders


Anatomical context of Language Development Disorders


Gene context of Language Development Disorders


Analytical, diagnostic and therapeutic context of Language Development Disorders


  1. Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase. Hogema, B.M., Gupta, M., Senephansiri, H., Burlingame, T.G., Taylor, M., Jakobs, C., Schutgens, R.B., Froestl, W., Snead, O.C., Diaz-Arrastia, R., Bottiglieri, T., Grompe, M., Gibson, K.M. Nat. Genet. (2001) [Pubmed]
  2. Autosomal recessive cerebellar hypoplasia. Mathews, K.D., Afifi, A.K., Hanson, J.W. J. Child Neurol. (1989) [Pubmed]
  3. 18q-syndrome and ectodermal dysplasia syndrome: description of a child and his family. Zannolli, R., Pierluigi, M., Pucci, L., Lagrasta, N., Gasparre, O., Matera, M.R., Di Bartolo, R.M., Mazzei, M.A., Sacco, P., Miracco, C., de Santi, M.M., Aitiani, P., Cavani, S., Pellegrini, L., Fimiani, M., Alessandrini, C., Galluzzi, P., Livi, W., Gonnelli, S., Terrosi-Vagnoli, P., Zappella, M., Morgese, G. Am. J. Med. Genet. A (2003) [Pubmed]
  4. 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) [Pubmed]
  5. 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) [Pubmed]
  6. Brain morphology in children with specific language impairment. Gauger, L.M., Lombardino, L.J., Leonard, C.M. J. Speech Lang. Hear. Res. (1997) [Pubmed]
  7. 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) [Pubmed]
  8. 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) [Pubmed]
  9. 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) [Pubmed]
  10. 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) [Pubmed]
  11. Central auditory processing disorder and ADHD. Jerome, L. Journal of the American Academy of Child and Adolescent Psychiatry. (2000) [Pubmed]
  12. 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) [Pubmed]
  13. 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) [Pubmed]
  14. Normal intrasylvian anatomical asymmetry in children with developmental language disorder. Preis, S., Jäncke, L., Schittler, P., Huang, Y., Steinmetz, H. Neuropsychologia. (1998) [Pubmed]
  15. Phenobarbital side effects: hyperactivity with speech delay. Levenstein, D., Gutgesell, M.E., Percy, P. Pediatrics (1984) [Pubmed]
  16. Urinary organic acid screening in children with developmental language delay. Michelson, M., Harel, S., Gutman, A., Lerman-Sagie, T. J. Inherit. Metab. Dis. (1999) [Pubmed]
  17. Focal grey matter heterotopias in monozygotic twins with developmental language disorder. Preis, S., Engelbrecht, V., Huang, Y., Steinmetz, H. Eur. J. Pediatr. (1998) [Pubmed]
  18. 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) [Pubmed]
  19. 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) [Pubmed]
  20. 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) [Pubmed]
  21. 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) [Pubmed]
  22. 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) [Pubmed]
  23. 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) [Pubmed]
  24. Special features of Graves' disease in early childhood. Segni, M., Leonardi, E., Mazzoncini, B., Pucarelli, I., Pasquino, A.M. Thyroid (1999) [Pubmed]
  25. 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) [Pubmed]
  26. 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) [Pubmed]
  27. 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) [Pubmed]
  28. Neurodevelopmental delay associated with nonconvulsive status epilepticus in a toddler. Shinawi, M., Shahar, E. J. Child Neurol. (2001) [Pubmed]
  29. Neurocognitive outcome in pediatric liver transplant recipients. Krull, K., Fuchs, C., Yurk, H., Boone, P., Alonso, E. Pediatric transplantation. (2003) [Pubmed]
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