Búsqueda | Biblioteca Virtual en Salud

1.

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

Tischfield, Max A; Baris, Hagit N; Wu, Chen; Rudolph, Guenther; Van Maldergem, Lionel; He, Wei; Chan, Wai-Man; Andrews, Caroline; Demer, Joseph L; Robertson, Richard L; Mackey, David A; Ruddle, Jonathan B; Bird, Thomas D; Gottlob, Irene; Pieh, Christina; Traboulsi, Elias I; Pomeroy, Scott L; Hunter, David G; Soul, Janet S; Newlin, Anna; Sabol, Louise J; Doherty, Edward J; de Uzcátegui, Clara E; de Uzcátegui, Nicolas; Collins, Mary Louise Z; Sener, Emin C; Wabbels, Bettina; Hellebrand, Heide; Meitinger, Thomas; de Berardinis, Teresa; Magli, Adriano; Schiavi, Costantino; Pastore-Trossello, Marco; Koc, Feray; Wong, Agnes M; Levin, Alex V; Geraghty, Michael T; Descartes, Maria; Flaherty, Maree; Jamieson, Robyn V; Møller, H U; Meuthen, Ingo; Callen, David F; Kerwin, Janet; Lindsay, Susan; Meindl, Alfons; Gupta, Mohan L; Pellman, David; Engle, Elizabeth C.

Cell ; 140(1): 74-87, 2010 Jan 08.

Artículo en Inglés | MEDLINE | ID: mdl-20074521

2.

[The IC3D classification of the corneal dystrophies]. / IC3D-Klassifikation von Hornhautdystrophien.

Weiss, J S; Møller, H U; Lisch, W; Kinoshita, S; Aldave, A J; Belin, M W; Kivelä, T; Busin, M; Munier, F L; Seitz, B; Sutphin, J; Bredrup, C; Mannis, M J; Rapuano, C; Van Rij, G; Kim, E K; Klintworth, G K.

Klin Monbl Augenheilkd ; 228 Suppl 1: S1-39, 2011 Jan.

Artículo en Alemán | MEDLINE | ID: mdl-21290351

3.

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

Eiberg, H; Møller, H U; Berendt, I; Mohr, J.

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

Artículo en Inglés | MEDLINE | ID: mdl-8044658

4.

Topographical arrangements of feline motor cortical projections onto the pretectum.

Flindt-Egebak, P; Møller, H U.

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

Artículo en Inglés | MEDLINE | ID: mdl-6527839

5.

Ophthalmic manifestations of congenital disorder of glycosylation type 1a.

Jensen, Hanne; Kjaergaard, Susanne; Klie, Flemming; Moller, H U.

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

Artículo en Inglés | MEDLINE | ID: mdl-12789572

6.

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

Barnicoat, A J; Moller, H U; Palmer, R W; Russell-Eggitt, I; Winter, R M.

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

Artículo en Inglés | MEDLINE | ID: mdl-8723565

7.

Reis-Bücklers dystrophy.

Møller, H U; Wittebolpost, D; Weidle, E G.

Cornea ; 25(4): 499; author reply 499-500, 2006 May.

Artículo en Inglés | MEDLINE | ID: mdl-16670500

8.

IC3D classification of corneal dystrophies.

Møller, H U; Weiss, Jayne S.

Dev Ophthalmol ; 48: 1-8, 2011.

Artículo en Inglés | MEDLINE | ID: mdl-21540628

9.

Corneal deposits associated with flecainide.

Møller, H U; Thygesen, K; Kruit, P J.

BMJ ; 302(6775): 506-7, 1991 Mar 02.

Artículo en Inglés | MEDLINE | ID: mdl-1901500

10.

[Follow-up study of patients after eye enucleation]. / Efterundersøgelse af øjenenukleerede patienter.

Møller, H U.

Ugeskr Laeger ; 145(20): 1528-30, 1983 May 16.

Artículo en Da | MEDLINE | ID: mdl-6879776

11.

[Von Hippel-Lindau disease--a multidisciplinary, underdiagnosed condition]. / Von Hippel-Lindaus sygdom--en multidisciplinaer, underdiagnosticeret tilstand.

Møller, H U.

Ugeskr Laeger ; 161(7): 969-70, 1999 Feb 15.

Artículo en Da | MEDLINE | ID: mdl-10051810

12.

[Iatrogenic tarsorrhaphy with cyanoacrylate]. / Iatrogen tarsorafi med cyanoakrylat.

Møller, H U; Marushak, D.

Ugeskr Laeger ; 145(3): 172-3, 1983 Jan 17.

Artículo en Da | MEDLINE | ID: mdl-6845470

13.

[Corneal erosions aggravated by local anesthetic eye-drops]. / Korneale erosioner forvaerret af lokalanaestetiske dråber.

Møller, H U; Ahrendt, N.

Ugeskr Laeger ; 145(3): 173-4, 1983 Jan 17.

Artículo en Da | MEDLINE | ID: mdl-6845471

14.

[Von Hippel-Lindau disease. A condition requiring multidisciplinary efforts]. / Von Hippel-Lindau's sygdom. En multidisciplinaer lidelse.

Møller, H U; Frimodt-Møller, P C; Haase, J; Dyreborg, U.

Ugeskr Laeger ; 148(6): 310-3, 1986 Feb 03.

Artículo en Da | MEDLINE | ID: mdl-3952860

15.

[Occlusion of the central retinal artery with scintigraphic demonstration of the source of emboli in the aorta]. / Arteria centralis retinae okklusioner med scintigrafisk påvist embolikilde i aorta.

Møller, H U; Marushak, D; Rasmussen, J W; Schmidt, K G.

Ugeskr Laeger ; 145(36): 2761-2, 1983 Sep 05.

Artículo en Da | MEDLINE | ID: mdl-6636339

16.

The IC3D classification of the corneal dystrophies.

Weiss, Jayne S; Møller, H U; Lisch, Walter; Kinoshita, Shigeru; Aldave, Anthony J; Belin, Michael W; Kivelä, Tero; Busin, Massimo; Munier, Francis L; Seitz, Berthold; Sutphin, John; Bredrup, Cecilie; Mannis, Mark J; Rapuano, Christopher J; Van Rij, Gabriel; Kim, Eung Kweon; Klintworth, Gordon K.

Cornea ; 27 Suppl 2: S1-83, 2008 Dec.

Artículo en Inglés, Español | MEDLINE | ID: mdl-19337156

17.

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

Møller, H U.

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

Artículo en Inglés | MEDLINE | ID: mdl-2694746

18.

Granular corneal dystrophy Groenouw type I. 115 Danish patients. An epidemiological and genetic population study.

Møller, H U.

Acta Ophthalmol (Copenh) ; 68(3): 297-303, 1990 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-2392905

19.

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

Møller, H U.

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

Artículo en Inglés | MEDLINE | ID: mdl-2220354

20.

Inter-familial variability and intra-familial similarities of granular corneal dystrophy Groenouw type I with respect to biomicroscopical appearance and symptomatology.

Møller, H U.

Acta Ophthalmol (Copenh) ; 67(6): 669-77, 1989 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-2618635

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

[The IC3D classification of the corneal dystrophies]. / IC3D-Klassifikation von Hornhautdystrophien.

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

Topographical arrangements of feline motor cortical projections onto the pretectum.

Ophthalmic manifestations of congenital disorder of glycosylation type 1a.

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

Reis-Bücklers dystrophy.

IC3D classification of corneal dystrophies.

Corneal deposits associated with flecainide.

[Follow-up study of patients after eye enucleation]. / Efterundersøgelse af øjenenukleerede patienter.

[Von Hippel-Lindau disease--a multidisciplinary, underdiagnosed condition]. / Von Hippel-Lindaus sygdom--en multidisciplinaer, underdiagnosticeret tilstand.

[Iatrogenic tarsorrhaphy with cyanoacrylate]. / Iatrogen tarsorafi med cyanoakrylat.

[Corneal erosions aggravated by local anesthetic eye-drops]. / Korneale erosioner forvaerret af lokalanaestetiske dråber.

[Von Hippel-Lindau disease. A condition requiring multidisciplinary efforts]. / Von Hippel-Lindau's sygdom. En multidisciplinaer lidelse.

[Occlusion of the central retinal artery with scintigraphic demonstration of the source of emboli in the aorta]. / Arteria centralis retinae okklusioner med scintigrafisk påvist embolikilde i aorta.

The IC3D classification of the corneal dystrophies.

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

Granular corneal dystrophy Groenouw type I. 115 Danish patients. An epidemiological and genetic population study.

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

Inter-familial variability and intra-familial similarities of granular corneal dystrophy Groenouw type I with respect to biomicroscopical appearance and symptomatology.