Items where Subject is "neurofibromatosis"
- CSHL Subject List (5)
- diseases & disorders (5)
- congenital hereditary genetic diseases (5)
- neurofibromatosis (5)
- congenital hereditary genetic diseases (5)
- diseases & disorders (5)
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Hannan, F., Ho, I., Tong, J. J., Zhu, Y., Nurnberg, P., Zhong, Y. (April 2006) Effect of neurofibromatosis type I mutations on a novel pathway for adenylyl cyclase activation requiring neurofibromin and Ras. Hum Mol Genet, 15 (7). pp. 1087-98. ISSN 0964-6906 (Print)
Ho, I. S., Hannan, F., Guo, H.-F., Hakker, I., Zhong, Y. (June 2007) Distinct functional domains of neurofibromatosis type 1 regulate immediate versus long-term memory formation. J Neurosci, 27 (25). pp. 6852-7. ISSN 1529-2401 (Electronic)
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Preiser, Samuel A., Davenport, Charles Benedict (October 1918) Multiple neurofibromatosis (Von Recklinghausen's disease) and its inheritance: With description of a case. American Journal of Medical Sciences, 156 (4). pp. 507-541.
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Silva, A. J., Elgersma, Y., Friedman, E., Stern, J., Kogan, J. (November 1998) A mouse model for learning and memory defects associated with neurofibromatosis type I. Pathol Biol (Paris), 46 (9). pp. 697-8. ISSN 0369-8114 (Print)
Silva, A. J., Frankland, P. W., Marowitz, Z., Friedman, E., Laszlo, G. S., Cioffi, D., Jacks, T., Bourtchuladze, R. (March 1997) A mouse model for the learning and memory deficits associated with neurofibromatosis type I. Nature Genetics, 15 (3). pp. 281-4. ISSN 1061-4036 (Print)