Ousager LB - Search Results

1

[Early-onset epileptic encephalopathy caused by CDKL5 mutation].

Hjalmgrim H, Hansen LK, Ousager LB, Møller RS. Hjalmgrim H, et al. Among authors: ousager lb. Ugeskr Laeger. 2014 Dec 15;176(25A):V01130031. Ugeskr Laeger. 2014. PMID: 25497626 Danish.

2

[Selenoprotein-related muscular dystrophy].

Hansen LK, Schrøder H, Ousager L. Hansen LK, et al. Ugeskr Laeger. 2011 Nov 28;173(48):3116-7. Ugeskr Laeger. 2011. PMID: 22118657 Danish.

3

[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation].

Jelsig AM, Tørring PM, Wikman F, Mortensen MB, Qvist N, Ousager LB. Jelsig AM, et al. Among authors: ousager lb. Ugeskr Laeger. 2014 Oct 27;176(44):V06130392. Ugeskr Laeger. 2014. PMID: 25354002 Danish.

4

[Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].

Jelsig AM, Tørring PM, Qvist N, Bernstein I, Ousager LB. Jelsig AM, et al. Among authors: ousager lb. Ugeskr Laeger. 2014 Oct 27;176(44):V06130391. Ugeskr Laeger. 2014. PMID: 25354001 Review. Danish.

5

[Genetic causes of infantile spasms--a systematic review].

Hansen LK, Ousager LB, Møller RS, Uldall PV, Hjalgrim H. Hansen LK, et al. Among authors: ousager lb. Ugeskr Laeger. 2012 Apr 23;174(17):1152-5. Ugeskr Laeger. 2012. PMID: 22533931 Review. Danish.

6

[Dravet syndrome diagnostics].

Hansen LK, Rasmussen NH, Ousager LB. Hansen LK, et al. Among authors: ousager lb. Ugeskr Laeger. 2010 Feb 22;172(8):626-7. Ugeskr Laeger. 2010. PMID: 20184820 Danish.

7

[Dravet syndrome].

Hansen LK, Rasmussen NH, Ousager LB. Hansen LK, et al. Among authors: ousager lb. Ugeskr Laeger. 2010 Feb 22;172(8):622-5. Ugeskr Laeger. 2010. PMID: 20184819 Danish.

8

Allelic dropout in the ENG gene, affecting the results of genetic testing in hereditary hemorrhagic telangiectasia.

Tørring PM, Kjeldsen AD, Ousager LB, Brasch-Andersen C, Brusgaard K. Tørring PM, et al. Among authors: ousager lb. Genet Test Mol Biomarkers. 2012 Dec;16(12):1419-23. doi: 10.1089/gtmb.2012.0230. Epub 2012 Oct 9. Genet Test Mol Biomarkers. 2012. PMID: 23046070

9

[Noonan syndrome can be diagnosed clinically and through molecular genetic analyses].

Henningsen MK, Jelsig AM, Andersen H, Brusgaard K, Ousager LB, Hertz JM. Henningsen MK, et al. Among authors: ousager lb. Ugeskr Laeger. 2015 Aug 3;177(32):V12140755. Ugeskr Laeger. 2015. PMID: 26321587 Review. Danish.

10

Hamartomatous polyposis syndromes: a review.

Jelsig AM, Qvist N, Brusgaard K, Nielsen CB, Hansen TP, Ousager LB. Jelsig AM, et al. Among authors: ousager lb. Orphanet J Rare Dis. 2014 Jul 15;9:101. doi: 10.1186/1750-1172-9-101. Orphanet J Rare Dis. 2014. PMID: 25022750 Free PMC article. Review.

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