IV. Neuroanatomy of Williams syndrome: A high-resolution MRI study

Journal of Cognitive Neuroscience

Volumn 12, Issue SUPPL. 1, 2000, Pages 65-73

  Reiss, Allan L ^a   Eliez, Stephan ^a   Schmitt, J Eric ^a   Straus, Erica ^a   Lai, Zona ^a   Jones, Wendy ^a   Bellugi, Ursula ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN SIZE; BRAIN STEM; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GRAY MATTER; HUMAN; MALE; NEUROANATOMY; NEURORADIOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; OCCIPITAL LOBE; PARIETAL LOBE; PRIORITY JOURNAL; WILLIAMS BEUREN SYNDROME;

EID: 0034044878     PISSN: 0898929X     EISSN: None     Source Type: Journal    
DOI: 10.1162/089892900561986     Document Type: Article

References (41)

1. Andreasen, N. C., Rajarethinam, R., Cizadlo, T., Arndt, S., Swayze H, V. W., Flashman, L. A., O'Leary, D. S., Ehrhardt, J. C., & Yuh, W. T. (1996). Automatic atlas-based volume-estimation of human brain regions from MR images. Journal of Computer Assisted Tomography, 20, 98-106.
2. Aylward, E. H., & Reiss, A. (1991). Area and volume measurement of posterior fossa structures in MRI. Journal of Psychiatric Research, 25, 159-168.
3. Bellugi, U., Bihrle, A., Jernigan, T., Trauner, D., & Doherty, S. (1990). Neuropsychological, neurological, and neuroanatomical profile of Williams syndrome. American Journal of Medical Genetics, Supplement, 6, 115-125.
4. Bellugi, U., Lichtenberger, L., Jones, W., Lai, Z., & St. George. M. (this volume). The neurocognitive profile of Williams syndrome: A complex pattern of strengths and weaknesses.
5. Bellugi, U., Lichtenberger, L., Mills, D., Galaburda, A., & Korenberg, J. (1999a). Bridging cognition, brain and molecular genetics: Evidence from Williams syndrome. Trends Neurosciences, 22, 197-207.
6. Bellugi, U., Mills, D., Jernigan, T., Hickok, G., & Galaburda, A. (1999b). Linking cognition, brain structure and brain function in Williams syndrome. In H. Tager-Flusberg (Ed.), Neurodevelopmental disorders: Contributions to a new framework from the cognitive neurosciences (pp. 111-136). Cambridge, MA: MIT Press.
7. Bellugi, U., Wang, P., & Jernigan, T. (1993). Williams syndrome: An unusual neuropsychological profile. In S. Broman & J. Grafman (Eds.), Atypical cognitive deficits in developmental disorders: Implications for brain function (pp. 23-56). Hillsdale, NJ: Erlbaum.
8. Demonet, J. F., Chollet, F., Ramsay, S., Cardebat, D., Nespoulous, J. L., Wise, R., Rascol, A., & Frackowiak, R. (1992). The anatomy of phonological and semantic processing in normal subjects. Brain, 115, 1753-1768.
9. Ewart, A. K., Morris, C. A., Atkinson, D., Jin, W., Sternes, K., Spallone, P., Stock, A., Leppert, M., & Keating, M. (1993). Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Mature Genetics, 5, 11-16.
10. Galaburda, A., & Bellugi, U. (this volume). Multi-level analysis of cortical neuroanatomy in Williams syndrome.
11. Galaburda, A., Wang, P. P., Bellugi, U., & Rosen, M. (1994). Cytoarchitectonic findings in a genetically-based disorder: Williams syndrome. NeuroReport, 5, 758-787.
12. Gosch, A., & Pankau, R. (1997). Personality characteristics and behaviour problems in individuals of different ages with Williams syndrome. Developmental Medicine and Child Neurology, 39, 527-533.
13. Harris-Collazo, M., Archibald, S., Lai, Z., Bellugi, U., & Jernigan, T. (1997). Morphological differences on quantitative MRI in Williams syndrome. Society for Neuroscience, New Orleans, LA.
14. Hickok, G., Bellugi, U., & Jones, W. (1995a). Asymmetrical ability [letter; comment]. Science, 270, 219-220.
15. Hickok, G., Neville, H., Mills, D., Jones, W., Rossen, M., & Bellugi, U. (1995b). Electrophysiological and quantitative MR analysis of the cortical auditory system in Williams syndrome. Cognitive Neuroscience Society Abstracts, 2, 66.
16. Jernigan, T. L., & Bellugi, U. (1990). Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome. Archives of Neurology, 47, 529-533.
17. Jernigan, T. L., Bellugi, U., Sowell, E., Doherty, S., & Hesselink, J. R. (1993). Cerebral morphologic distinctions between Williams and Down syndromes. Archives of Neurology, 50, 186-191.
18. Jones, K. L. (1990). Williams syndrome: An historical perspective of its evolution, natural history, and etiology. American Journal of Medical Genetics, Supplement, 6, 89-96.
19. Kaplan, D. M., Liu, A. M., Abrams, M. T., Warsofsky, I. S., Kates, W. R., White, C. D., Kaufmann, W. E., & Reiss, A. (1997). Application of an automated parcellation method to the analysis of pediatric brain volumes. Psychiatry Research, 76, 15-27.
20. Kates, W. R., Warsofsky, I. S., Patwardhan, A., Abrams, M. T., Liu, A., Kaufmann, W. E., Naidu, S., & Reiss, A. L. (1999). Automated Talairach-based parcellation and measurement of cerebral lobes in children. Psychiatry Research, 91, 11-30.
21. Korenberg, J., Chen, X.-N., Hirota, H., Lai, Z., Bellugi, U., Burian, D., Roc, B., & Matsuoka, R. (this volume). Genome structure and cognitive map of Williams syndrome.
22. Korenberg, J., Chen, X.-N., Lai, Z., Yimlamai, D., Bisighini, R., & Bellugi, U. (1997a). Williams syndrome: The search for the genetic origins of cognition. American Journal of Human Genetics, 61, 103.
23. Korenberg, J., Chen, X.-N., Mirchell, S., & Sun, Z., (1997b). The genomic organization of Williams syndrome. International Behavioral Neuroscience Society Abstracts, 6, 59.
24. Korenberg, J., Chen, X.-N., Mirchell, S., Sun, Z.-G., Hubert, R., Vataru, E., & Bellugi, U. (1996). The genomic organization of Williams syndrome. American Journal of Human Genetics (Supplement), 59, A306.
25. Lenhoff, H. M., Wang, P. P., Greenberg, F., & Bellugi, U. (1997). Williams syndrome and the brain. Scientific American, 277, 68-73.
26. Liegeois-Chauvel, C., Peretz, I., Babai, M., Laguitton, V., & Chauvel, P. (1998). Contribution of different cortical areas in the temporal lobes to music processing [see comments]. Brain, 121, 1853-1867.
27. Lowery, M. C., Morris, C. A., Ewart, A., Brothman, L. J., Zhu, X. L., Leonard, C., Carey, J., Keating, M., & Rothman, A. (1995). Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: Evaluation of 235 patients. American Journal of Human Genetics, 57, 49-53.
28. Morris, C. A., Demsey, S. A., Leonard, C. O., Dilts, C., & Blackburn, B. L. (1988). Natural history of Williams syndrome: Physical characteristics. Journal of Pediatrics, 113, 318-326.
29. Nakayama, T., Matsuoka, R., Kimura, M., Hirota, H., Mikoshiba, K., Shimizu, Y., Shimizu, N., & Akagawa, K. (1998). Hemizygous deletion of the HPC-1/syntaxin 1A gene (STX1A) in patients with Williams syndrome. Cytogenetics and Cell Genetics, 82, 49-51.
30. Pantev, C., Oostenveld, R., Engelien, A., Ross, B., Roberts, L. E., & Hoke, M. (1998). Increased auditory cortical representation in musicians [see comments]. Nature, 392, 811-814.
31. Price, C., Wise, R., Ramsay, S., Friston, K., Howard, D., Patterson, K., & Frackowiak, R. (1992). Regional response differences within the human auditory cortex when listening to words. Neuroscience Letters, 146, 179-182.
32. Reiss, A. L. (1999).BrainImage. Stanford, CA: Stanford University.
33. Reiss, A. L., Hennessey, J. G., Rubin, M., Beach, L., Abrams, M. T., Warsofsky, I. S., Liu, A. M. C., et al. (1998). Reliability and validity of an algorithm for fuzzy tissue segmentation of magnetic resonance images. Journal of Computer-Assisted Tomography, 22, 471-479.
34. Schlosser, M. J., et al. (1998). Functional MRI studies of auditory comprehension. Human Brain Mapping, 6, 1-13.
35. Sirevaag, A. M., Black, J. E., Shafron, D., & Greenough, W. T. (1988). Direct evidence that complex experience increases capillary branching and surface area in visual cortex of young rats. Brain Research, 471, 299-304.
36. Subramanium, B., Hennessey, J. G., Rubin, M. A., Beach, L. S., & Reiss, A. L. (1997). Software and methods for quantitative imaging in neuroscience: The Kennedy Krieger Institute Human Brain Project. In S. H. Koslow & M.F. Huerta (Eds.), Neuroinformatics: An overview of the human brain project (pp. 335-360). Hillsdale, NJ: Erlbaum.
37. Wang, J. Y., Frenzel, K. E., Wen, D., & Falls, D. L. (1998). Transmembrane neuregulins interact with LIM kinase 1, a cytoplasmic protein kinase implicated in development of visuospatial cognition. Journal of Biological Chemistry, 273, 20525-20534.
38. Wang, P. P., Hesselink, J. R., Jernigan, T. L., Doherty, S., & Bellugi, U. (1992). Specific neurobehavioral profile of Williams syndrome is associated with neocerebellar hemispheric preservation. Neurology, 42, 1999-2002.
39. Wang, Y. K., Samos, C. H., Peoples, R., Perez-Jurado, L. A., Nusse, R., & Francke, U. (1997). A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23. Human Molecular Genetics, 6, 465-472.
40. Williams Syndrome Association 6th National/International Professional Conference Abstracts. (1994). Genetic Counseling, 6, 131-192.
41. Zatorre, R. J., Evans, A. C., & Meyer, E. (1994). Neural mechanisms underlying melodic perception and memory for pitch. Journal of Neuroscience, 14, 1908-1919.