Koefoed P - Search Results

1

Reduced regional cerebral blood flow in SPG4-linked hereditary spastic paraplegia.

Scheuer KH, Nielsen JE, Krabbe K, Simonsen C, Koefoed P, Sørensen SA, Gade A, Paulson OB, Law I. Scheuer KH, et al. Among authors: koefoed p. J Neurol Sci. 2005 Aug 15;235(1-2):23-32. doi: 10.1016/j.jns.2005.03.051. J Neurol Sci. 2005. PMID: 15939438

2

Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia.

Svenstrup K, Bross P, Koefoed P, Hjermind LE, Eiberg H, Born AP, Vissing J, Gyllenborg J, Nørremølle A, Hasholt L, Nielsen JE. Svenstrup K, et al. Among authors: koefoed p. J Neurol Sci. 2009 Sep 15;284(1-2):90-5. doi: 10.1016/j.jns.2009.04.024. Epub 2009 May 6. J Neurol Sci. 2009. PMID: 19423133

3

Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

Nielsen JE, Johnsen B, Koefoed P, Scheuer KH, Grønbech-Jensen M, Law I, Krabbe K, Nørremølle A, Eiberg H, Søndergård H, Dam M, Rehfeld JF, Krarup C, Paulson OB, Hasholt L, Sørensen SA. Nielsen JE, et al. Among authors: koefoed p. Eur J Neurol. 2004 Dec;11(12):817-24. doi: 10.1111/j.1468-1331.2004.00888.x. Eur J Neurol. 2004. PMID: 15667412

4

Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG4) using direct mutation detection.

Nielsen JE, Koefoed P, Kjaergaard S, Jensen LN, Nørremølle A, Hasholt L. Nielsen JE, et al. Among authors: koefoed p. Prenat Diagn. 2004 May;24(5):363-6. doi: 10.1002/pd.875. Prenat Diagn. 2004. PMID: 15164410

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

Urodynamic evaluation of patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.

Jensen LN, Gerstenberg T, Kallestrup EB, Koefoed P, Nordling J, Nielsen JE. Jensen LN, et al. Among authors: koefoed p. J Neurol Neurosurg Psychiatry. 1998 Nov;65(5):693-6. doi: 10.1136/jnnp.65.5.693. J Neurol Neurosurg Psychiatry. 1998. PMID: 9810939 Free PMC article.

8

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

9

Increased blood BDNF in healthy individuals with a family history of depression.

Knorr U, Søndergaard MHG, Koefoed P, Jørgensen A, Faurholt-Jepsen M, Vinberg M, Kessing LV. Knorr U, et al. Among authors: koefoed p. Psychiatry Res. 2017 Oct;256:176-179. doi: 10.1016/j.psychres.2017.06.057. Epub 2017 Jun 17. Psychiatry Res. 2017. PMID: 28645077

10

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

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