H. Møller

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IC3D Classification of Corneal Dystrophies—Edition 2

B. Seitz, T. Kivelä, C. Rapuano, 2015, Cornea.

The IC3D classification of the corneal dystrophies.

B. Seitz, T. Kivelä, C. Rapuano, 2008, Cornea.

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

H. Fledelius, D. Milewicz, E. Regalado, 2012, British Journal of Ophthalmology.

Vibeke Harbud, The Danish association for von Hippel-Lindau patients and their relatives

L. Sunde, A. Gerdes, C. Thomsen, 2013 .

von Hippel-Lindau disease: Surveillance strategy for endolymphatic sac tumors

M. Kosteljanetz, C. Thomsen, M. Bisgaard, 2011, Genetics in Medicine.

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

R. Winter, R. Palmer, A. Barnicoat, 1996, Clinical dysmorphology.

Diagnosis of tumours in anterior and middle cranial fossae.

M. Bardram, H. Møller, 1952, Acta ophthalmologica.

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

T. Meitinger, Mohan L Gupta, D. Hunter, 2010, Cell.

Ophthalmic manifestations of congenital disorder of glycosylation type 1a

S. Kjaergaard, H. Jensen, F. Klie, 2003, Ophthalmic genetics.

Assignment of Granular Corneal Dystrophy Groenouw Type I (CDGG1) to Chromosome 5q

H. Eiberg, J. Mohr, H. Møller, 1994, European journal of human genetics : EJHG.

Familial Benign Recurrent Cranial Nerve Palsies

H. Møller, J. Gordon Klee, 1984 .

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

J. Kiilgaard, M. Bisgaard, M. Galanakis, 2017, British Journal of Ophthalmology.

TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy

Janice S. Lee, F. Collins, E. Jabs, 2021, Human Genetics.

IC3D classification of corneal dystrophies.

C. Rapuano, M. Belin, M. Mannis, 2011, Developments in ophthalmology.

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

N. Ehlers, M. Bojsen-Møller, A. Ridgway, 1993, Acta ophthalmologica.

Von Hippel-Lindau disease (vHL): National clinical guideline for diagnosis and surveillance in Denmark

M. Kosteljanetz, L. Ousager, L. Sunde, 2013 .

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

H. Møller, 1989, Acta ophthalmologica.

Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene

A. Ridgway, H. Møller, 2000 .

Granular corneal dystrophy Groenouw type I: Clinical aspects and treatment

H. U. Møller, H. Møller, 1990, Acta ophthalmologica.

Granular corneal dystrophy Groenouw type I

A. Ridgway, H. U. Møller, H. Møller, 1990, Acta ophthalmologica.

Immunoglobulins in granular corneal dystrophy Groenouw type I

M. Bojsen-Møller, M. E. Nelson, H. U. Møller, 1993, Acta ophthalmologica.

Granular corneal dystrophy Groenouw type I 115 Danish patients

H. Møller, 1990, Acta ophthalmologica.

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

H. Eiberg, T. Kruse, H. U. Møller, 1989, Acta ophthalmologica.

Granular corneal dystrophy Groenouw type I (Grl) and Reis‐Bücklers' corneal dystrophy (R‐B) One Entity?

H. U. Møller, H. Møller, 1989, Acta ophthalmologica.

Dystrophy: a revised definition.

M. Warburg, H. U. Møller, H. Møller, 1989, Journal of medical genetics.

Genetics of granular dystrophy.

A. Ridgway, H. U. Møller, H. Møller, 1992, Ophthalmology.

IC 3 D-Klassifikation von Hornhautdystrophien 1 The IC3D Classification of the Corneal Dystrophies

B. Seitz, T. Kivelä, C. Rapuano, 2011 .

[The IC3D classification of the corneal dystrophies].

B. Seitz, T. Kivelä, C. Rapuano, 2011, Klinische Monatsblatter fur Augenheilkunde.

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

H. Møller, J. Hansen, 2017, Neuropediatrics.

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

M. Kirchhoff, T. Bryndorf, A. Bisgaard, 2007, Clinical dysmorphology.

Excessive myopia and glaucoma.

H. U. Møller, H. Møller, 1948, Acta ophthalmologica.

[Applicability of nebacetin in ophthalmology].

B. Lawaetz, H. Møller, G. Østerberg, 1953, Ugeskrift for læger.

von Hippel-Lindau disease: Updated guideline for diagnosis and surveillance.

B. Stausbøl‐Grøn, L. Ousager, L. Sunde, 2022, European journal of medical genetics.

Von Hippel-Lindau disease (vHL)

M. Kosteljanetz, L. Ousager, L. Sunde, 2013 .

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

M. Kosteljanetz, L. Sunde, A. Gerdes, 2013, Danish medical journal.

The IC3D classification of the corneal dystrophies.

C. Rapuano, M. Belin, M. Mannis, 2008, Cornea.

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

H. Møller, 1992, Ophthalmic paediatrics and genetics.

Dot‐Map‐Fingerprint Dystrophy—Cogan's Microcystic Dystrophy—Normal reactions of The Corneal Epithelium?

N. Ehlers, H. U. Møller, H. Møller, 1987, Acta ophthalmologica. Supplement.

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

N. Ehlers, H. U. Møller, H. Møller, 1988, Acta ophthalmologica.