Jensen H - Search Results

1

[Genetic testing and counselling in inherited eye disease].

Brøndum-Nielsen K, Jensen H, Timshel S, Grønskov K, Larsen M. Brøndum-Nielsen K, et al. Among authors: jensen h. Ugeskr Laeger. 2013 Sep 2;175(36):2031-4. Ugeskr Laeger. 2013. PMID: 23992910 Review. Danish.

2

Blepharophimosis, corneal vascularization, deafness, and acroosteolysis: a "new" syndrome?

Warburg M, Ullman S, Jensen H, Pedersen H, Kobayashi T, Russell B, Tranebjaerg L, Richard G, Brøndum-Nielsen K. Warburg M, et al. Among authors: jensen h. Am J Med Genet A. 2006 Dec 15;140(24):2709-13. doi: 10.1002/ajmg.a.31543. Am J Med Genet A. 2006. PMID: 17103436

3

Axonal loss occurs early in dominant optic atrophy.

Milea D, Sander B, Wegener M, Jensen H, Kjer B, Jørgensen TM, Lund-Andersen H, Larsen M. Milea D, et al. Among authors: jensen h. Acta Ophthalmol. 2010 May;88(3):342-6. doi: 10.1111/j.1755-3768.2008.01469.x. Epub 2009 Mar 19. Acta Ophthalmol. 2010. PMID: 19302076 Free article.

4

[The genetic background for the eye malformations anophthalmia and microphthalmia].

Roos LS, Grønskov K, Jensen H, Tümer Z. Roos LS, et al. Among authors: jensen h. Ugeskr Laeger. 2012 Mar 12;174(11):713-6. Ugeskr Laeger. 2012. PMID: 22409892 Danish.

5

Absence of NR2E1 mutations in patients with aniridia.

Corso-Díaz X, Borrie AE, Bonaguro R, Schuetz JM, Rosenberg T, Jensen H, Brooks BP, Macdonald IM, Pasutto F, Walter MA, Grønskov K, Brooks-Wilson A, Simpson EM. Corso-Díaz X, et al. Among authors: jensen h. Mol Vis. 2012;18:2770-82. Epub 2012 Nov 22. Mol Vis. 2012. PMID: 23213277 Free PMC article.

6

Prevalence and diagnostic spectrum of generalized retinal dystrophy in Danish children.

Bertelsen M, Jensen H, Larsen M, Lorenz B, Preising MN, Rosenberg T. Bertelsen M, et al. Among authors: jensen h. Ophthalmic Epidemiol. 2013 Jun;20(3):164-9. doi: 10.3109/09286586.2013.776692. Epub 2013 May 10. Ophthalmic Epidemiol. 2013. PMID: 23662838

7

A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia.

Roos L, Fang M, Dali C, Jensen H, Christoffersen N, Wu B, Zhang J, Xu R, Harris P, Xu X, Grønskov K, Tümer Z. Roos L, et al. Among authors: jensen h. Clin Genet. 2014 Sep;86(3):276-81. doi: 10.1111/cge.12277. Epub 2013 Oct 25. Clin Genet. 2014. PMID: 24024553

8

Ocular phenotype analysis of a family with biallelic mutations in the BEST1 gene.

Sharon D, Al-Hamdani S, Engelsberg K, Mizrahi-Meissonnier L, Obolensky A, Banin E, Sander B, Jensen H, Larsen M, Schatz P. Sharon D, et al. Among authors: jensen h. Am J Ophthalmol. 2014 Mar;157(3):697-709.e1-2. doi: 10.1016/j.ajo.2013.12.010. Epub 2013 Dec 15. Am J Ophthalmol. 2014. PMID: 24345323

9

Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function.

Roos L, Bertelsen B, Harris P, Bygum A, Jensen H, Grønskov K, Tümer Z. Roos L, et al. Among authors: jensen h. BMC Med Genet. 2015 Jun 23;16:40. doi: 10.1186/s12881-015-0179-9. BMC Med Genet. 2015. PMID: 26099342 Free PMC article.

10

OPTICAL COHERENCE TOMOGRAPHY IN JUVENILE NEURONAL CEROID LIPOFUSCINOSIS.

Hansen MS, Hove MN, Jensen H, Larsen M. Hansen MS, et al. Among authors: jensen h. Retin Cases Brief Rep. 2016 Spring;10(2):137-9. doi: 10.1097/ICB.0000000000000200. Retin Cases Brief Rep. 2016. PMID: 26308342 Free PMC article.

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