A. Langmann

发表

K. Laczika, C. Marosi, D. Fuchs, 2005, Annals of Hematology.

Women underrepresented on editorial boards of 60 major medical journals.

T. Pieber, A. Langmann, A. Fahrleitner-Pammer, 2011, Gender medicine.

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

M. Stratton, P. Futreal, R. Wooster, 2006, Nature Genetics.

Shawnta S. Friday-Stroud, Earnest Friday, Anna L. Green, 2005, Annals of Hematology.

Ward, A. Langmann, A. Siegle, 2008, Circulation journal : official journal of the Japanese Circulation Society.

K. Laczika, C. Marosi, D. Fuchs, 1984, Veterinary Record.

[Vitreoretinal changes in siblings of two patients with Stickler syndrome. Study of two families].

A. Langmann, G. Langmann, J. Faulborn, 1993, Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft.

Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.

Irene Gottlob, A. S. Anil Kumar, Andrea Langmann, 2008, Brain : a journal of neurology.

Polytetrafluoroethylene (Goretex) for muscle elongation in the surgical treatment of strabismus with restricted motility.

A. Langmann, S. Lindner, W. Wackernagel, 2005, Acta ophthalmologica Scandinavica.

Bestrahlungsbehandlung der endokrinen Orbitopathie – State of the Art

P. Schedlbauer, A. Langmann, A. Hackl, 2001 .

Molecular characterization of a unique de novo 15q deletion associated with Prader–Willi syndrome and central visual impairment

C. Windpassinger, A. Langmann, E. Petek, 2003, Clinical genetics.

Predictive diagnosis of the cancer prone Li–Fraumeni syndrome by accident: new challenges through whole genome array testing

M. Speicher, A. Obenauf, A. Langmann, 2009, Journal of Medical Genetics.

Systemic and Ophthalmic Manifestations in Different Types of Refractive Errors in Patients with Down Syndrome

M. Tesic, A. Langmann, G. Dimitrova, 2022, Medicina.

Zur Differenzialdiagnose des Exophthalmus

A. Langmann, S. Lindner, 2004, Der Ophthalmologe.

Ocular sequelae of multimodal therapy of hematologic malignancies in children.

I. Slavc, A. Langmann, G. Langmann, 1994, Medical and pediatric oncology.

[Endocrine orbitopathy--diagnosis].

A. Langmann, S. Lindner, 2001, Acta medica Austriaca.

Normalisation of asymmetric astigmatism after intralesional steroid injection for upper eye lid hemangioma in childhood

A. Langmann, S. Lindner, 2005, Documenta Ophthalmologica.

Ophthalmological findings in three patients with cholesterol acyltransferase deficiency syndrome before and after kidney transplantation

J. Horina, A. Langmann, G. Langmann, 1993, Graefe's Archive for Clinical and Experimental Ophthalmology.

Acute concomitant esotropia in children

A. Langmann, S. Lindner, D. Ivastinović, 2018, Acta ophthalmologica.

The Relation between Reading Skills and Eye Movement Patterns in Adolescent Readers: Evidence from a Regular Orthography

Christof Körner, Florian B. Pokorny, Andrea Langmann, 2016, PloS one.

Congenital third nerve palsy in septo-optic dysplasia

A. Langmann, S. Lindner, 2004, British Journal of Ophthalmology.

Biomechanical analysis of x-pattern exotropia.

T. Haslwanter, R. Hoerantner, T. Kaltofen, 2011, American journal of ophthalmology.

Akupunktur bei Retinitis pigmentosa

G. Litscher, B. Feigl, A. Langmann, 2000, Spektrum der Augenheilkunde.

Reduction of the dose to the lens in prophylactic cranial irradiation: a comparison of three different treatment techniques and two different beam qualities.

A. Langmann, G. Stücklschweiger, A. Hackl, 1992, International journal of radiation oncology, biology, physics.

Acute Bilateral Tonic Pupil in a Child.

A. Langmann, H. Hubmann, M. Brandner, 2017, JAMA ophthalmology.

Repeated mobility testing for later artificial visual function evaluation

M Velikay-Parel, R Hornig, G Dagnelie, 2007, Journal of neural engineering.

The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

Mervyn G. Thomas, R. Hertle, P. Tarpey, 2011, Brain : a journal of neurology.

Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

M. Stratton, P. Futreal, R. Wooster, 2011, Nature Genetics.

[Low-Vision Training For Better Usage of Magnifying Visual Aids].

A. Langmann, S. Lindner, E. Kollegger, 1994, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.

Biomechanical analysis of x-pattern exotropia.

T. Haslwanter, R. Hoerantner, T. Kaltofen, 2011, American journal of ophthalmology.

Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.

P. Tarpey, F. Proudlock, I. Gottlob, 2008, Brain : a journal of neurology.

The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

Mervyn G. Thomas, R. Hertle, P. Tarpey, 2011, Brain : a journal of neurology.

[Two patients with xerophthalmia].

U. Stelzl, A. Langmann, M. Bachernegg, 2000, Klinische Monatsblatter fur Augenheilkunde.