C. Lindholm

Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease

H. Feldman, B. Leavitt, S. Butland, 2006, BMC neurology.

Localized laryngeal amyloidosis: partial characterization of an amyloid fibril protein AL.

K. Sletten, P. Westermark, J. Natvig, 1982, Molecular immunology.

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

S. Melquist, D. Neary, B. Boeve, 2006, Nature.

Age-associated micronuclei containing centromeres and the X chromosome in lymphocytes of women

H. Norppa, S. Knuutila, M. Wessman, 1995 .

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17.

S. Melquist, H. Feldman, A. Sadovnick, 2006, Brain : a journal of neurology.

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

H. Feldman, M. Hutton, G. Hsiung, 2006, Brain : a journal of neurology.

Identification of single amino acid substitutions in the staphylococcal nuclease protein that enhance and diminish T cell clone recognition of naturally processed peptides.

A. Finnegan, K. Seamon, C. Lindholm, 1992, International Immunology.