Нейропсихологический анализ патологии мозолистого тела - Мария Ковязина

Woodruff P. W., McManus I.C., David A. S. Meta-analysis of corpuscallosum size in schizophrenia // Journal of Neurology, Neurosurgery and Psychiatry. 1995. V. 58. № 4. P. 457–461.

Woodruff P. W., Phillips M. L., Rushe T., Wright I. C., Murray R. M., David A. S. Corpus callosum size and inter-hemispheric function in schizophrenia // Schizophrenia Research. 1997. V. 23. № 3. P. 189–196.

Yakovlev P. I., Lecours A. R. The myelogenetic cycles of regional maturation of the brain // Regional Development of the brain in early life / Minkowski A. (Ed). – Boston (MA): Blackwell Scientific Publications, 1967. P. 3–70.

Yazgan Y., Kinsbourne M. Functional consequences of changes in callosal area in Tourette's syndrome and Attention Deficit/ Hyperactivity Disorder // The Parallel Brain: The Cognitive Neuroscience of the Corpus Callosum (Issues in Clinical and Cognitive Neuropsychology) / E. Zaidel, M. Iacoboni (Eds.). – Cambridge (MA): The MIT Press, 2003. P. 423–432.

Zaidel D. W. The case for a relationship between human memory, hippocampus, and corpus callosum // Biological Research. 1995. V. 28. P. 51–57.

Zaidel E., Aboitiz F., Clarke J. Sexual dimorphism in interhemispheric relations: anatomical-behavioral convergence // Biological Research. 1995. V. 28. № 1. P. 27–43.

Zaidel E., Iacoboni M. New insights in callosal anatomy and morphometry // The Parallel Brain: The Cognitive Neuroscience of the Corpus Callosum (Issues in Clinical and Cognitive Neuropsychology) / E. Zaidel, M. Iacoboni (Eds.). – Cambridge (MA): The MIT Press, 2003. P. 131–136.

Zaidel D. W., Sperry R. W. Memory impairment after commissurotomy in man // Brain. 1974. V. 97. № 1. P. 263–272.

Zweier C., Thiel C. T., Dufke A., Crow Y. J., Meinecke P., Suri M., Ala-Mello S., Beemer F., Bernasconi S., Bianchi P., Bier A., Devriendt K., Dimitrov B., Firth H., Gallagher R. C., Garavelli L., Gillessen-Kaesbach G., Hudgins L., Kaariainen H., Karstens S., Krantz I., Mannhardt A., Medne L., Mucke J., Kibaek M., Krogh L. N., Peippo M., Rittinger O., Schulz S., Schelley S. L., Temple I. K., Dennis N. R., Van der Knaap M. S., Wheeler P., Yerushalmi B., Zenker M., Seidel H., Lachmeijer A., Prescott T., Kraus C., Lowry R. B., Rauch A. Clinical and mutational spectrum of Mowat-Wilson syndrome // European Journal of Medical Genetics. 2005. V. 48. № 2. P. 97–111.