Health Survey of Adults with Neurofibromatosis 1 Compared to Population Study Controls

Author:

Fjermestad Krister W.,Nyhus Livø,Kanavin Øivind J.,Heiberg Arvid,Hoxmark Lise B.

Publisher

Wiley

Subject

Genetics(clinical)

Reference40 articles.

1. Abramowicz, A., & Gos, M. (2014). Neurofibromin in neurofibromatosis type 1—mutations in NF1gene as a cause of disease. Developmental Period Medicine, 18(3), 297–306.

2. Agaimy, A., Vassos, N., & Croner, R. S. (2012). Gastrointestinal manifestations of neurofibromatosis type 1 (Recklinghausen’s disease): clinicopathological spectrum with pathogenetic considerations. International Journal of Clinical and Experimental Pathology, 5(9), 852–862.

3. Barton, B., & North, K. (2004). Social skills of children with neurofibromatosis type 1. Developmental Medicine and Child Neurology, 46(8), 553–563. https://doi.org/10.1017/s0012162204000921

4. Bicudo, N. P., de Menezes Neto, B. F., da Silva de Avo, L. R., Ramos Germano, C. M., & Melo, D. G. (2016). Quality of life in adults with neurofibromatosis 1 in Brazil. Journal of Genetic Counseling, 25(5), 1063–1074. https://doi.org/10.1007/s10897-016-9939-8

5. Birch, P., & Friedman, J. M. (2012). Quality of life in NF1. In M. Upadhyaya & D. N. Cooper (Eds.), Neurofibromatosis type 1 (pp. 93–103). Berlin: Springer-Verlag.

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