Koefoed P - Search Results

1

Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.

Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC. Milman N, et al. Among authors: koefoed p. Ann Hematol. 2005 Mar;84(3):146-9. doi: 10.1007/s00277-004-0865-8. Epub 2004 Mar 23. Ann Hematol. 2005. PMID: 15042317

2

HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.

Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC. Koefoed P, et al. Scand J Clin Lab Invest. 2002;62(7):527-35. doi: 10.1080/003655102321004549. Scand J Clin Lab Invest. 2002. PMID: 12512743

3

Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods.

Milman N, Koefoed P, Pedersen P, Nielsen FC, Eiberg H. Milman N, et al. Among authors: koefoed p. Eur J Haematol. 2003 Dec;71(6):403-7. doi: 10.1046/j.0902-4441.2003.00156.x. Eur J Haematol. 2003. PMID: 14703688

4

Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1.

Koefoed P, Hasholt L, Fenger K, Nielsen JE, Eiberg H, Buschard K, Sørensen SA. Koefoed P, et al. Hum Genet. 1998 Nov;103(5):564-9. doi: 10.1007/s004390050870. Hum Genet. 1998. PMID: 9860298

5

CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.

Nielsen JE, Koefoed P, Abell K, Hasholt L, Eiberg H, Fenger K, Niebuhr E, Sørensen SA. Nielsen JE, et al. Among authors: koefoed p. Hum Mol Genet. 1997 Oct;6(11):1811-6. doi: 10.1093/hmg/6.11.1811. Hum Mol Genet. 1997. PMID: 9302257

6

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study.

Nielsen JE, Krabbe K, Jennum P, Koefoed P, Jensen LN, Fenger K, Eiberg H, Hasholt L, Werdelin L, Sørensen SA. Nielsen JE, et al. Among authors: koefoed p. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):61-6. doi: 10.1136/jnnp.64.1.61. J Neurol Neurosurg Psychiatry. 1998. PMID: 9436729 Free PMC article.

7

Procholecystokinin as marker of human Ewing sarcomas.

Reubi JC, Koefoed P, Hansen Tv, Stauffer E, Rauch D, Nielsen FC, Rehfeld JF. Reubi JC, et al. Among authors: koefoed p. Clin Cancer Res. 2004 Aug 15;10(16):5523-30. doi: 10.1158/1078-0432.CCR-1015-03. Clin Cancer Res. 2004. PMID: 15328192

8

No association between the -399 C > T polymorphism of the neuropeptide Y gene and schizophrenia, unipolar depression or panic disorder in a Danish population.

Lindberg C, Koefoed P, Hansen ES, Bolwig TG, Rehfeld JF, Mellerup E, Jørgensen OS, Kessing LV, Werge T, Haugbøl S, Wang AG, Woldbye DP. Lindberg C, et al. Among authors: koefoed p. Acta Psychiatr Scand. 2006 Jan;113(1):54-8. doi: 10.1111/j.1600-0447.2005.00648.x. Acta Psychiatr Scand. 2006. PMID: 16390370

9

Symptomatic type 1 protein C deficiency caused by a de novo Ser270Leu mutation in the catalytic domain.

Lind B, Koefoed P, Thorsen S. Lind B, et al. Among authors: koefoed p. Br J Haematol. 2001 Jun;113(3):642-8. doi: 10.1046/j.1365-2141.2001.02809.x. Br J Haematol. 2001. PMID: 11380450 Free article.

10

Common variants of the ACE gene and aneurysmal subarachnoid hemorrhage in a Danish population: a case-control study.

Staalsø JM, Nielsen M, Edsen T, Koefoed P, Springborg JB, Moltke FB, Laursen H, Nielsen HB, Olsen NV. Staalsø JM, et al. Among authors: koefoed p. J Neurosurg Anesthesiol. 2011 Oct;23(4):304-9. doi: 10.1097/ANA.0b013e318225c979. J Neurosurg Anesthesiol. 2011. PMID: 21709586

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