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Page 1
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
[Patients with severe chronic neutropenia].
Amundsen HF, Stray-Pedersen A, Tjønnfjord GE, Abrahamsen TG. Amundsen HF, et al. Among authors: abrahamsen tg. Tidsskr Nor Laegeforen. 2003 Mar 6;123(5):621-3. Tidsskr Nor Laegeforen. 2003. PMID: 12683187 Free article. Norwegian. No abstract available.
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.
[Chronic neutropenia--subtypes and treatment].
Amundsen HF, Stray-Pedersen A, Tjønnfjord GE, Abrahamsen TG. Amundsen HF, et al. Among authors: abrahamsen tg. Tidsskr Nor Laegeforen. 2003 Mar 6;123(5):624-6. Tidsskr Nor Laegeforen. 2003. PMID: 12683188 Review. Norwegian. No abstract available.
Alpha fetoprotein is increasing with age in ataxia-telangiectasia.
Stray-Pedersen A, Borresen-Dale AL, Paus E, Lindman CR, Burgers T, Abrahamsen TG. Stray-Pedersen A, et al. Among authors: abrahamsen tg. Eur J Paediatr Neurol. 2007 Nov;11(6):375-80. doi: 10.1016/j.ejpn.2007.04.001. Epub 2007 May 30. Eur J Paediatr Neurol. 2007. PMID: 17540590
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.
Stray-Pedersen A, Backe PH, Sorte HS, Mørkrid L, Chokshi NY, Erichsen HC, Gambin T, Elgstøen KB, Bjørås M, Wlodarski MW, Krüger M, Jhangiani SN, Muzny DM, Patel A, Raymond KM, Sasa GS, Krance RA, Martinez CA, Abraham SM, Speckmann C, Ehl S, Hall P, Forbes LR, Merckoll E, Westvik J, Nishimura G, Rustad CF, Abrahamsen TG, Rønnestad A, Osnes LT, Egeland T, Rødningen OK, Beck CR; Baylor-Johns Hopkins Center for Mendelian Genomics; Boerwinkle EA, Gibbs RA, Lupski JR, Orange JS, Lausch E, Hanson IC. Stray-Pedersen A, et al. Among authors: abrahamsen tg. Am J Hum Genet. 2014 Jul 3;95(1):96-107. doi: 10.1016/j.ajhg.2014.05.007. Epub 2014 Jun 12. Am J Hum Genet. 2014. PMID: 24931394 Free PMC article.
A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction.
Sorte HS, Osnes LT, Fevang B, Aukrust P, Erichsen HC, Backe PH, Abrahamsen TG, Kittang OB, Øverland T, Jhangiani SN, Muzny DM, Vigeland MD, Samarakoon P, Gambin T, Akdemir ZH, Gibbs RA, Rødningen OK, Lyle R, Lupski JR, Stray-Pedersen A. Sorte HS, et al. Among authors: abrahamsen tg. Mol Genet Genomic Med. 2016 Sep 17;4(6):604-616. doi: 10.1002/mgg3.237. eCollection 2016 Nov. Mol Genet Genomic Med. 2016. PMID: 27896283 Free PMC article.
124 results