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CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome.
Notarangelo LD, Peitsch MC, Abrahamsen TG, Bachelot C, Bordigoni P, Cant AJ, Chapel H, Clementi M, Deacock S, de Saint Basile G, Duse M, Espanol T, Etzioni A, Fasth A, Fischer A, Giliani S, Gomez L, Hammarstorm L, Jones A, Kanariou M, Kinnon C, Klemola T, Kroczek RA, Levy J, Matamoros N, Monafo V, Paolucci P, Reznick I, Sanal O, Smith CI, Thompson RA, Tovo P, Villa A, Vihinen M, Vossen J, Zegers BJ. Notarangelo LD, et al. Among authors: abrahamsen tg. Immunol Today. 1996 Nov;17(11):511-6. doi: 10.1016/0167-5699(96)30059-5. Immunol Today. 1996. PMID: 8961627
The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parents.
Stray-Pedersen A, Jónsson T, Heiberg A, Lindman CR, Widing E, Aaberge IS, Borresen-Dale AL, Abrahamsen TG. Stray-Pedersen A, et al. Among authors: abrahamsen tg. Clin Exp Immunol. 2004 Jul;137(1):179-86. doi: 10.1111/j.1365-2249.2004.02492.x. Clin Exp Immunol. 2004. PMID: 15196260 Free PMC article.
Clinical spectrum of X-linked hyper-IgM syndrome.
Levy J, Espanol-Boren T, Thomas C, Fischer A, Tovo P, Bordigoni P, Resnick I, Fasth A, Baer M, Gomez L, Sanders EA, Tabone MD, Plantaz D, Etzioni A, Monafo V, Abinun M, Hammarstrom L, Abrahamsen T, Jones A, Finn A, Klemola T, DeVries E, Sanal O, Peitsch MC, Notarangelo LD. Levy J, et al. Among authors: abrahamsen t. J Pediatr. 1997 Jul;131(1 Pt 1):47-54. doi: 10.1016/s0022-3476(97)70123-9. J Pediatr. 1997. PMID: 9255191
Primary immunodeficiency diseases in Norway.
Stray-Pedersen A, Abrahamsen TG, Frøland SS. Stray-Pedersen A, et al. Among authors: abrahamsen tg. J Clin Immunol. 2000 Nov;20(6):477-85. doi: 10.1023/a:1026416017763. J Clin Immunol. 2000. PMID: 11202238
157 results