B. Jurklies

发表

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

E. Aller, I. Ebermann, H. Scholl, 2007, Human Genetics.

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

S. Bolz, B. Jurklies, J. Heckenlively, 2009, Proceedings of the National Academy of Sciences.

Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia.

E. Zrenner, T. Rosenberg, B. Jurklies, 2011, Human molecular genetics.

OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.

E. Zrenner, B. Jurklies, B. Wissinger, 2001, Human molecular genetics.

Monitoring retinal function in neovascular maculopathy using multifocal electroretinography – early and long-term correlation with clinical findings

E. Sutter, B. Jurklies, N. Bornfeld, 2002, Graefe's Archive for Clinical and Experimental Ophthalmology.

Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy.

E. Zrenner, B. Jurklies, D. Besch, 1997, Biochemical and biophysical research communications.

Photodynamic therapy of subfoveal choroidal neovascularization in pathologic myopia with verteporfin. 1-year results of a randomized clinical trial--VIP report no. 1.

George A. Williams, M. Blumenkranz, S. Harding, 2001, Ophthalmology.

Photodynamic Therapy Using Verteporfin for Choroidal Neovascularization Associated with Angioid Streaks – Long-Term Effects

B. Jurklies, N. Bornfeld, H. Schilling, 2006, Ophthalmic Research.

A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.

B. Lorenz, H. Stöhr, B. Jurklies, 2000, American journal of human genetics.

Mapping and genomic characterization of the gene encoding diacylglycerol kinase γ (DAGK3): assessment of its role in dominant optic atrophy (OPA1)

M. Schmid, H. Stöhr, B. Jurklies, 1999, Human Genetics.

Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration

B. Lorenz, B. Jurklies, F. Holz, 2000, European Journal of Human Genetics.

Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F‐mediated inherited retinal disorders

J. Sahel, C. Jubin, T. de Ravel, 2019, Human mutation.

Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophy

B. Jurklies, E. De Baere, B. Wissinger, 2014, Molecular genetics & genomic medicine.

Intraocular biopsy using special forceps: a new instrument and refined surgical technique

B. Jurklies, N. Bornfeld, F. Otterbach, 2010, British Journal of Ophthalmology.

[Comparison of superselective intraarterial fibrinolysis with conservative therapy. Use in patients with acute non-arteritic central retinal artery occlusion].

C. Schmoor, B. Jurklies, H. Brückmann, 2010, Der Ophthalmologe.

Angiotensin II in the rabbit retina

E. Zrenner, B. Jurklies, E. Guenther, 1997, Visual Neuroscience.

Multicenter study of the European Assessment Group for Lysis in the Eye (EAGLE) for the treatment of central retinal artery occlusion: design issues and implications. EAGLE Study report no. 1

C. Schmoor, B. Jurklies, A. Neubauer, 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome

A. V. Cideciyan, T. Aleman, A. Cideciyan, 2004, Human mutation.

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

P. Sieving, S. Jacobson, R. Salati, 2005, European Journal of Human Genetics.

CNGA3 mutations in hereditary cone photoreceptor disorders.

S. Jacobson, R. Salati, L. Sharpe, 2001, American journal of human genetics.

Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene

S. Jacobson, T. de Ravel, B. Lorenz, 2019, Human mutation.

Vascular Tumors of the Retina

C. Shields, B. Jurklies, W. Green, 2007 .

Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.

K Rohrschneider, L I van den Born, M J van Schooneveld, 2001, American journal of human genetics.

[Endoresection of large uveal melanomas after pretreatment by single-dose stereotactic convergence irradiation with the leksell gamma knife--first experience on 46 cases].

G. Horstmann, B. Jurklies, N. Bornfeld, 2006, Klinische Monatsblatter fur Augenheilkunde.

Positional cloning of the gene associated with X-linked juvenile retinoschisis

B. Lorenz, B. Jurklies, A. Marquardt, 1997, Nature Genetics.

Central retinal artery occlusion: local intra-arterial fibrinolysis versus conservative treatment, a multicenter randomized trial.

C. Schmoor, B. Jurklies, L. Solymosi, 2010, Ophthalmology.

Course of pattern-reversed visual evoked cortical potentials in 30 eyes after bony orbital decompression in dysthyroid optic neuropathy

B. Jurklies, K. Mann, J. Esser, 2010, British Journal of Ophthalmology.

Neuromodulatory effects of the renin-angiotensin system on the cat electroretinogram.

E. Zrenner, B. Jurklies, H. Osswald, 1994, Investigative ophthalmology & visual science.

Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X‐linked retinitis pigmentosa

B. Jurklies, D. Besch, C. Pusch, 2002, Human mutation.

Ophthal- Mology Ophthal- Mology Springer International Study of the Retinal Fiber Layer in Patients with Acquired Immunodeficiency Syndrome 1 Anterior Proliferative Vitreoretinopathy in Trauma and Complicated Retinal Detachment. a Histopathologic Study 15 Evaluation of Eyes Harbouring Perfluorocarbo

Springer-Verlag, Köln, F. Fankhauser, 2022 .

Photodynamic therapy for symptomatic choroidal hemangioma: visual and anatomic results.

U. Schmidt-Erfurth, B. Jurklies, S. Michels, 2002, Ophthalmology.

Bietti's crystalline dystrophy of the retina and cornea.

B. Jurklies, A. Wessing, C. Jurklies, 1999, Retina.

Cholinergic effects on cat retinain vitro: Changes in rod- and cone-drivenb-wave and optic nerve response

B. Jurklies, A. Kaelin-Lang, G. Niemeyer, 1996, Vision Research.

LONG-TERM EFFECT OF ACETAZOLAMIDE TREATMENT OF PATIENTS WITH UVEITIC CHRONIC CYSTOID MACULAR EDEMA IS LIMITED BY PERSISTING INFLAMMATION

A. Heiligenhaus, B. Jurklies, N. Bornfeld, 2005, Retina.

Cardiovascular Risk Factors in Central Retinal Artery Occlusion: Results of a Prospective and Standardized Medical Examination.

R. Wachter, C. Schmoor, B. Jurklies, 2015, Ophthalmology.

EFEMP1 is not associated with sporadic early onset drusen

B. Jurklies, G. Rudolph, U. Kellner, 2001, Ophthalmic genetics.

Ruthenium-106 plaque brachytherapy for symptomatic vasoproliferative tumours of the retina

B. Jurklies, A. Schueler, N. Bornfeld, 2006, British Journal of Ophthalmology.

The Role of Photodynamic Therapy in Retinal Vascular Disease

B. Jurklies, N. Bornfeld, 2007 .

Photodynamic therapy using verteporfin in circumscribed choroidal haemangioma

U. Schmidt-Erfurth, B. Jurklies, N. Bornfeld, 2003, The British journal of ophthalmology.

The role of photodynamic therapy in the treatment of symptomatic choroidal hemangioma

B. Jurklies, N. Bornfeld, 2005, Graefe's Archive for Clinical and Experimental Ophthalmology.

Photodynamic therapy with verteporfin in paediatric and young adult patients: long-term treatment results of choroidal neovascularisations

B. Jurklies, N. Bornfeld, A. Lipski, 2008, British Journal of Ophthalmology.

Effects of adenosinergic agents on the vascular resistance and on the optic nerve response in the perfused cat eye

B. Jurklies, A. Kaelin-Lang, G. Niemeyer, 1999, Vision Research.

[Corneoretinal dystrophy (Bietti)-- Long-term course of one patient over a period of 30 years, and interindividual variability of clinical and electrophysiological findings in two patients].

B. Jurklies, N. Bornfeld, A. Wessing, 2001, Klinische Monatsblatter fur Augenheilkunde.

MULTIFOCAL ELECTRORETINOGRAPHY IN PATIENTS WITH EXUDATIVE AMD AND INTRAVITREAL TREATMENT WITH PEGAPTANIB SODIUM

B. Jurklies, N. Bornfeld, A. Lipski, 2007, Retina.

Photodynamic therapy of subfoveal choroidal neovascularization in pathologic myopia with verteporfin - 1-year results of a randomized clinical trial - VIP report no. 1

Philip D. Harvey, M. Blumenkranz, N. Bressler, 2001 .

[Retinitis pigmentosa--clinical, genetic and pathophysiologic aspects].

E. Zrenner, B. Jurklies, A. Wessing, 1997, Klinische Monatsblatter fur Augenheilkunde.

Intraocular biopsy using special forceps: a new instrument and refined surgical technique

B. Jurklies, N. Bornfeld, F. Otterbach, 2010, British Journal of Ophthalmology.

Brachytherapy Of Juxtapapillary Uveal Melanoma Using Notched Ruthenium-106 Ophthalmic Plaques

Norbert Bornfeld, Wolfgang Sauerwein, B. Jurklies, 2008 .