Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 52

1.

[Diagnosis, monitoring and treatment of tuberous sclerosis complex].

Reinhard M, Sunde L, Madsen MG, Andersen BN, Bendstrup E, Sommerlund M, Gjørup H, Larsen DA, Møller HU, Nielsen DG, Mortensen UM, Handrup MM, Aagaard NKM, Cortnum S, Khatir DS, Bayat M, Andersen G, Stausbøl-Grøn B, Christensen J.

Ugeskr Laeger. 2019 Nov 4;181(45). pii: V05190293. Danish.

PMID:
31791451
2.

The Corneal Dystrophies-Does the Literature Clarify or Confuse?

Weiss JS, Møller HU, Lisch W.

Am J Ophthalmol. 2018 Nov;195:xv-xvii. doi: 10.1016/j.ajo.2018.07.047. Epub 2018 Sep 11. No abstract available.

PMID:
30217469
3.

Retinal hemangioblastoma: prevalence, incidence and frequency of underlying von Hippel-Lindau disease.

Binderup MLM, Stendell AS, Galanakis M, Møller HU, Kiilgaard JF, Bisgaard ML.

Br J Ophthalmol. 2018 Jul;102(7):942-947. doi: 10.1136/bjophthalmol-2017-310884. Epub 2017 Sep 28.

PMID:
28972023
4.

Is Tadpole Pupil in an Adolescent Girl Caused by Denervation Hypersensitivity?

Hansen JK, Møller HU.

Neuropediatrics. 2017 Jun;48(3):185-187. doi: 10.1055/s-0036-1597614. Epub 2017 Jan 4.

PMID:
28052304
5.

IC3D classification of corneal dystrophies--edition 2.

Weiss JS, Møller HU, Aldave AJ, Seitz B, Bredrup C, Kivelä T, Munier FL, Rapuano CJ, Nischal KK, Kim EK, Sutphin J, Busin M, Labbé A, Kenyon KR, Kinoshita S, Lisch W.

Cornea. 2015 Feb;34(2):117-59. doi: 10.1097/ICO.0000000000000307. Erratum in: Cornea. 2015 Oct;34(10):e32.

PMID:
25564336
6.

Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition.

Binderup ML, Bisgaard ML, Harbud V, Møller HU, Gimsing S, Friis-Hansen L, Hansen Tv, Bagi P, Knigge U, Kosteljanetz M, Bøgeskov L, Thomsen C, Gerdes AM, Ousager LB, Sunde L; Danish vHL Coordination Group.

Dan Med J. 2013 Dec;60(12):B4763.

PMID:
24355456
7.

[Idiopathic intracranial hypertension is a rare cause of headache in children].

Viuff AC, Hansen JK, Møller HU.

Ugeskr Laeger. 2013 Mar 4;175(10):661-2. Danish.

PMID:
23462040
8.

Prevalence of corneal dystrophies in the United States: estimates from claims data.

Møller HU, Sunde L.

Invest Ophthalmol Vis Sci. 2013 Jan 14;54(1). pii: 387. doi: 10.1167/iovs.12-11211. No abstract available.

PMID:
23319566
9.

Eye features in three Danish patients with multisystemic smooth muscle dysfunction syndrome.

Moller HU, Fledelius HC, Milewicz DM, Regalado ES, Ostergaard JR.

Br J Ophthalmol. 2012 Sep;96(9):1227-31. doi: 10.1136/bjophthalmol-2011-301462. Epub 2012 Jul 11.

10.

von Hippel-Lindau disease: surveillance strategy for endolymphatic sac tumors.

Poulsen ML, Gimsing S, Kosteljanetz M, Møller HU, Brandt CA, Thomsen C, Bisgaard ML.

Genet Med. 2011 Dec;13(12):1032-41. doi: 10.1097/GIM.0b013e31822beab1.

PMID:
21912262
11.

Genotype of lattice corneal dystrophy (R124C mutation in TGFBI) in a patient presenting with features of Avellino corneal dystrophy.

Lisch W, Moller HU.

Cornea. 2011 Aug;30(8):949; author reply 949-50. doi: 10.1097/ICO.0b013e3182031e5c. No abstract available.

PMID:
21617530
12.

IC3D classification of corneal dystrophies.

Møller HU, Weiss JS.

Dev Ophthalmol. 2011;48:1-8. doi: 10.1159/000324074. Epub 2011 Apr 26. Review.

PMID:
21540628
13.

[The IC3D classification of the corneal dystrophies].

Weiss JS, Møller HU, Lisch W, Kinoshita S, Aldave AJ, Belin MW, Kivelä T, Busin M, Munier FL, Seitz B, Sutphin J, Bredrup C, Mannis MJ, Rapuano C, Van Rij G, Kim EK, Klintworth GK.

Klin Monbl Augenheilkd. 2011 Jan;228 Suppl 1:S1-39. doi: 10.1055/s-0029-1245895. Epub 2011 Feb 2. German.

PMID:
21290351
14.

Pediatric corneal dystrophies. A plea for pictures.

Hu M, Kestelyn P, Weiss JS.

Cornea. 2010 Dec;29(12):1469. doi: 10.1097/ICO.0b013e3181e9b540. No abstract available.

PMID:
20847666
15.

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.

Tischfield MA, Baris HN, Wu C, Rudolph G, Van Maldergem L, He W, Chan WM, Andrews C, Demer JL, Robertson RL, Mackey DA, Ruddle JB, Bird TD, Gottlob I, Pieh C, Traboulsi EI, Pomeroy SL, Hunter DG, Soul JS, Newlin A, Sabol LJ, Doherty EJ, de Uzcátegui CE, de Uzcátegui N, Collins ML, Sener EC, Wabbels B, Hellebrand H, Meitinger T, de Berardinis T, Magli A, Schiavi C, Pastore-Trossello M, Koc F, Wong AM, Levin AV, Geraghty MT, Descartes M, Flaherty M, Jamieson RV, Møller HU, Meuthen I, Callen DF, Kerwin J, Lindsay S, Meindl A, Gupta ML Jr, Pellman D, Engle EC.

Cell. 2010 Jan 8;140(1):74-87. doi: 10.1016/j.cell.2009.12.011.

16.

The IC3D classification of the corneal dystrophies.

Weiss JS, Møller HU, Lisch W, Kinoshita S, Aldave AJ, Belin MW, Kivelä T, Busin M, Munier FL, Seitz B, Sutphin J, Bredrup C, Mannis MJ, Rapuano CJ, Van Rij G, Kim EK, Klintworth GK.

Cornea. 2008 Dec;27 Suppl 2:S1-83. doi: 10.1097/ICO.0b013e31817780fb. Review. English, Spanish.

17.

Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata.

Bisgaard AM, Rasmussen LN, Møller HU, Kirchhoff M, Bryndorf T.

Clin Dysmorphol. 2007 Apr;16(2):109-12.

PMID:
17351355
18.

Reis-Bücklers dystrophy.

Møller HU, Wittebolpost D, Weidle EG.

Cornea. 2006 May;25(4):499; author reply 499-500. No abstract available.

PMID:
16670500
19.

Ophthalmic manifestations of congenital disorder of glycosylation type 1a.

Jensen H, Kjaergaard S, Klie F, Moller HU.

Ophthalmic Genet. 2003 Jun;24(2):81-8.

PMID:
12789572
20.

[Von Hippel-Lindau disease--a multidisciplinary, underdiagnosed condition].

Møller HU.

Ugeskr Laeger. 1999 Feb 15;161(7):969-70. Danish. No abstract available.

PMID:
10051810
21.

Recurrent ophthalmoplegia in childhood: diagnostic and etiologic considerations.

Ostergaard JR, Møller HU, Christensen T.

Cephalalgia. 1996 Jun;16(4):276-9.

PMID:
8792041
22.

An unusual presentation of Smith-Magenis syndrome with iris dysgenesis.

Barnicoat AJ, Moller HU, Palmer RW, Russell-Eggitt I, Winter RM.

Clin Dysmorphol. 1996 Apr;5(2):153-8.

PMID:
8723565
23.

Assignment of granular corneal dystrophy Groenouw type I (CDGG1) to chromosome 5q.

Eiberg H, Møller HU, Berendt I, Mohr J.

Eur J Hum Genet. 1994;2(2):132-8.

PMID:
8044658
24.

Differential diagnosis between granular corneal dystrophy Groenouw type I and paraproteinemic crystalline keratopathy.

Møller HU, Ehlers N, Bojsen-Møller M, Ridgway AE.

Acta Ophthalmol (Copenh). 1993 Aug;71(4):552-5.

PMID:
8249591
25.

Immunoglobulins in granular corneal dystrophy Groenouw type I.

Møller HU, Bojsen-Møller M, Schrøder HD, Nelson ME, Vegge T.

Acta Ophthalmol (Copenh). 1993 Aug;71(4):548-51.

PMID:
8249590
26.

Genetics of granular dystrophy.

Ridgway AE, Moller HU.

Ophthalmology. 1992 Dec;99(12):1753. No abstract available.

PMID:
1480387
27.

Recessively inherited, simple optic atrophy--does it exist?

Møller HU.

Ophthalmic Paediatr Genet. 1992 Mar;13(1):31-2. No abstract available.

PMID:
1594192
28.

Corneal deposits associated with flecainide.

Møller HU, Thygesen K, Kruit PJ.

BMJ. 1991 Mar 2;302(6775):506-7. No abstract available.

29.

Granular corneal dystrophy Groenouw type I. Clinical and genetic aspects.

Møller HU.

Acta Ophthalmol Suppl. 1991;(198):1-40. Review. No abstract available.

PMID:
1651039
30.

Granular corneal dystrophy Groenouw type I. Clinical aspects and treatment.

Møller HU.

Acta Ophthalmol (Copenh). 1990 Aug;68(4):384-9.

PMID:
2220354
31.
32.

Granular corneal dystrophy Groenouw type I. A report of a probable homozygous patient.

Møller HU, Ridgway AE.

Acta Ophthalmol (Copenh). 1990 Feb;68(1):97-101.

PMID:
2336942
33.

Granular corneal dystrophy Groenouw type I (GrI) and Reis-Bücklers' corneal dystrophy (R-B). One entity?

Møller HU.

Acta Ophthalmol (Copenh). 1989 Dec;67(6):678-84. Review.

PMID:
2694746
34.

Linkage relations of the locus for granular corneal dystrophy Groenouw type I with 35 polymorphic systems.

Møller HU, Eiberg H, Kruse TA.

Acta Ophthalmol (Copenh). 1989 Dec;67(6):721-3.

PMID:
2618643
36.

Dystrophy: a revised definition.

Warburg M, Møller HU.

J Med Genet. 1989 Dec;26(12):769-71.

37.

Pathology and pathomechanisms of epithelial microcystic and basement membrane abnormalities of the cornea.

Ehlers N, Møller HU.

Acta Ophthalmol (Copenh). 1988 Jun;66(3):318-26.

PMID:
10994455
38.

Dot-map-fingerprint dystrophy--Cogan's microcystic dystrophy--normal reactions of the corneal epithelium?

Ehlers N, Møller HU.

Acta Ophthalmol Suppl. 1987;182:62-6. No abstract available.

PMID:
2837064
39.

[Von Hippel-Lindau disease. A condition requiring multidisciplinary efforts].

Møller HU, Frimodt-Møller PC, Haase J, Dyreborg U.

Ugeskr Laeger. 1986 Feb 3;148(6):310-3. Danish. No abstract available.

PMID:
3952860
40.

Early treatment of granular dystrophy (Groenouw type I).

Møller HU, Ehlers N.

Acta Ophthalmol (Copenh). 1985 Oct;63(5):597-600.

PMID:
3907260
41.

Topographical arrangements of feline motor cortical projections onto the pretectum.

Flindt-Egebak P, Møller HU.

Neurosci Lett. 1984 Nov 23;52(1-2):85-9.

PMID:
6527839
42.

[Occlusion of the central retinal artery with scintigraphic demonstration of the source of emboli in the aorta].

Møller HU, Marushak D, Rasmussen JW, Schmidt KG.

Ugeskr Laeger. 1983 Sep 5;145(36):2761-2. Danish. No abstract available.

PMID:
6636339
43.

[Follow-up study of patients after eye enucleation].

Møller HU.

Ugeskr Laeger. 1983 May 16;145(20):1528-30. Danish. No abstract available.

PMID:
6879776
44.

[Corneal erosions aggravated by local anesthetic eye-drops].

Møller HU, Ahrendt N.

Ugeskr Laeger. 1983 Jan 17;145(3):173-4. Danish. No abstract available.

PMID:
6845471
45.

[Iatrogenic tarsorrhaphy with cyanoacrylate].

Møller HU, Marushak D.

Ugeskr Laeger. 1983 Jan 17;145(3):172-3. Danish. No abstract available.

PMID:
6845470
46.

Therapeutic value of nebacetin in ophthalmology.

LAWAETZ B, MØLLER HU, ØSTERBERG G.

Am J Ophthalmol. 1953 Dec;36(12):1686-7. No abstract available.

PMID:
13104582
47.

[Applicability of nebacetin in ophthalmology].

Lawaetz B, Møller HU, Østerberg G.

Ugeskr Laeger. 1953 Jan 29;115(5):166-8. Undetermined Language. No abstract available.

PMID:
13077828
48.

Diagnosis of tumours in anterior and middle cranial fossae.

Bardram M, Møller HU.

Acta Ophthalmol (Copenh). 1952;30(1):65-96. No abstract available.

PMID:
12985282
49.

[Arrangements for ophthalmological service at the hospital].

MØLLER HU.

Ugeskr Laeger. 1950 May 25;112(21):767-72. Undetermined Language. No abstract available.

PMID:
15443119
50.

Om farvesansundersøgelser.

MØLLER HU.

Ugeskr Laeger. 1948 Feb 12;110(7):182. Undetermined Language. No abstract available.

PMID:
18859177

Supplemental Content

Loading ...
Support Center