PubMed

[Arthrogryposis multiplex congenita and retinitis pigmentosa.]

Stübiger N, Biester S, Deuter C, Zrenner E, Besch D.

Ophthalmologe. 2009 Jun 6. [Epub ahead of print] German. PMID: 19499227 [PubMed - as supplied by publisher]Related articles

Full macular translocation (FMT) versus photodynamic therapy (PDT) with verteporfin in the treatment of neovascular age-related macular degeneration: 2-year results of a prospective, controlled, randomised pilot trial (FMT-PDT).

Lüke M, Ziemssen F, Völker M, Altpeter E, Beutel J, Besch D, Bartz-Schmidt KU, Gelisken F.

Graefes Arch Clin Exp Ophthalmol. 2009 Jun;247(6):745-54. Epub 2009 Feb 12.PMID: 19214552 [PubMed - indexed for MEDLINE]Related articles

[Abnormal head turn in a patient with Brown's syndrome]

van Waveren M, Krzizok T, Besch D.

Klin Monbl Augenheilkd. 2008 Aug;225(8):731-4. German. PMID: 18712660 [PubMed - indexed for MEDLINE]Related articles

Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patients.

Besch D, Sachs H, Szurman P, Gülicher D, Wilke R, Reinert S, Zrenner E, Bartz-Schmidt KU, Gekeler F.

Br J Ophthalmol. 2008 Oct;92(10):1361-8. Epub 2008 Jul 28.PMID: 18662916 [PubMed - indexed for MEDLINE]Related articles

[Ocular neuromyotonia after radiation therapy]

van Waveren M, Herzau V, Besch D.

Ophthalmologe. 2009 Jan;106(1):47-51. German. PMID: 18607604 [PubMed - indexed for MEDLINE]Related articles

Visual field defects in acute optic neuritis--distribution of different types of defect pattern, assessed with threshold-related supraliminal perimetry, ensuring high spatial resolution.

Nevalainen J, Krapp E, Paetzold J, Mildenberger I, Besch D, Vonthein R, Keltner JL, Johnson CA, Schiefer U.

Graefes Arch Clin Exp Ophthalmol. 2008 Apr;246(4):599-607. Epub 2008 Feb 1.PMID: 18239928 [PubMed - indexed for MEDLINE]Related articles

Reading performance with low-vision aids and vision-related quality of life after macular translocation surgery in patients with age-related macular degeneration.

Nguyen NX, Besch D, Bartz-Schmidt K, Gelisken F, Trauzettel-Klosinski S.

Acta Ophthalmol Scand. 2007 Dec;85(8):877-82. Epub 2007 Jul 25.PMID: 17651462 [PubMed - indexed for MEDLINE]Related articles

Full macular translocation versus photodynamic therapy with verteporfin in the treatment of neovascular age-related macular degeneration: 1-year results of a prospective, controlled, randomised pilot trial (FMT-PDT).

Gelisken F, Voelker M, Schwabe R, Besch D, Aisenbrey S, Szurman P, Grisanti S, Herzau V, Bartz-Schmidt KU.

Graefes Arch Clin Exp Ophthalmol. 2007 Aug;245(8):1085-95.PMID: 17219106 [PubMed - indexed for MEDLINE]Related articles

Dose, timing and frequency of subconjunctival 5-fluorouracil injections after glaucoma filtering surgery.

Reinthal EK, Denk PO, Grüb M, Besch D, Bartz-Schmidt KU.

Graefes Arch Clin Exp Ophthalmol. 2007 Mar;245(3):369-75. Epub 2006 Oct 17.PMID: 17043809 [PubMed - indexed for MEDLINE]Related articles

[Choroidal effusion syndrome after embolization of an indirect cavernous sinus fistula via the superior ophthalmic vein]

Karim-Zade K, Mielke J, Besch D, Szurman P, Ernemann U, Herzau V.

Ophthalmologe. 2006 Jul;103(7):609-11. German. PMID: 16685540 [PubMed - indexed for MEDLINE]Related articles

[Genetic diseases of the eye]

Besch D, Rudolph G.

Klin Monbl Augenheilkd. 2005 Dec;222(12):955-71. German. PMID: 16380882 [PubMed - indexed for MEDLINE]Related articles

Delayed otogenic hydrocephalus after acute otitis media in pediatric patients: the changing presentation of a serious otologic complication.

Koitschev A, Simon C, Löwenheim H, Kumpf M, Besch D, Ernemann U.

Acta Otolaryngol. 2005 Nov;125(11):1230-5.PMID: 16353408 [PubMed - indexed for MEDLINE]Related articles

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.

Schuster A, Weisschuh N, Jägle H, Besch D, Janecke AR, Zierler H, Tippmann S, Zrenner E, Wissinger B.

Br J Ophthalmol. 2005 Oct;89(10):1258-64.PMID: 16170112 [PubMed - indexed for MEDLINE]Related articlesFree article

Progressive cone dystrophy with deutan genotype and phenotype.

Scholl HP, Kremers J, Besch D, Zrenner E, Jägle H.

Graefes Arch Clin Exp Ophthalmol. 2006 Feb;244(2):183-91. Epub 2005 Aug 5.PMID: 16082559 [PubMed - indexed for MEDLINE]Related articles

Glare sensitivity and professional drivers' safety: a case of rod-cone dystrophy with negative electroretinogram.

Jägle H, Besch D.

Acta Ophthalmol Scand. 2005 Aug;83(4):504-7.PMID: 16029280 [PubMed - indexed for MEDLINE]Related articles

Neuroprotective effects of cardiotrophin-like cytokine on retinal ganglion cells.

Schuettauf F, Zurakowski D, Quinto K, Varde MA, Besch D, Laties A, Anderson R, Wen R.

Graefes Arch Clin Exp Ophthalmol. 2005 Oct;243(10):1036-42. Epub 2005 Oct 20.PMID: 15838664 [PubMed - indexed for MEDLINE]Related articles

Abducens nerve paresis in spontaneous intracranial hypotension syndrome.

Grueb M, Besch D, Mielke J, Reinthal E, Herzau V.

Acta Ophthalmol Scand. 2005 Apr;83(2):269-70. No abstract available. PMID: 15799754 [PubMed - indexed for MEDLINE]Related articles

Uveitis in children.

Zierhut M, Michels H, Stübiger N, Besch D, Deuter C, Heiligenhaus A.

Int Ophthalmol Clin. 2005 Spring;45(2):135-56. Review. No abstract available. PMID: 15791163 [PubMed - indexed for MEDLINE]Related articles

[Spontaneous ocular pulsation]

Besch D, El-Araj I, Mielke J, Herzau V.

Ophthalmologe. 2005 Oct;102(10):1000-1, 1002. German. No abstract available. PMID: 15455254 [PubMed - indexed for MEDLINE]Related articles

Visual short-term effects of Viagra: double-blind study in healthy young subjects.

Jägle H, Jägle C, Sérey L, Yu A, Rilk A, Sadowski B, Besch D, Zrenner E, Sharpe LT.

Am J Ophthalmol. 2004 May;137(5):842-9.PMID: 15126148 [PubMed - indexed for MEDLINE]Related articles

Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects.

Besch D, Jägle H, Scholl HP, Seeliger MW, Zrenner E.

Vision Res. 2003 Dec;43(28):3095-108. Review.PMID: 14611947 [PubMed - indexed for MEDLINE]Related articles

Further support for digenic inheritance in Bardet-Biedl syndrome.

Fauser S, Munz M, Besch D.

J Med Genet. 2003 Aug;40(8):e104. No abstract available. PMID: 12920096 [PubMed - indexed for MEDLINE]Related articlesFree article

Multifocal ERG changes in patients with ocular Behçet's disease during therapy with interferon alpha 2a.

Stübiger N, Besch D, Deuter CM, Zierhut M, Kötter I.

Adv Exp Med Biol. 2003;528:529-32. No abstract available. PMID: 12918757 [PubMed - indexed for MEDLINE]Related articles

MfERG waveform characteristics in the RS1h mouse model featuring a 'negative' ERG.

Seeliger MW, Weber BH, Besch D, Zrenner E, Schrewe H, Mayser H.

Doc Ophthalmol. 2003 Jul;107(1):37-44.PMID: 12906120 [PubMed - indexed for MEDLINE]Related articles

Prevention and therapy in hereditary retinal degenerations.

Besch D, Zrenner E.

Doc Ophthalmol. 2003 Jan;106(1):31-5. Review.PMID: 12675483 [PubMed - indexed for MEDLINE]Related articles

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

Pusch CM, Broghammer M, Jurklies B, Besch D, Jacobi FK.

Hum Mutat. 2002 Nov;20(5):405.PMID: 12402343 [PubMed - indexed for MEDLINE]Related articles

Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy.

Fauser S, Leo-Kottler B, Besch D, Luberichs J.

Ophthalmic Genet. 2002 Sep;23(3):191-7.PMID: 12324878 [PubMed - indexed for MEDLINE]Related articles

Leber's hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery.

Leo-Kottler B, Luberichs J, Besch D, Christ-Adler M, Fauser S.

Graefes Arch Clin Exp Ophthalmol. 2002 Sep;240(9):758-64. Epub 2002 Aug 2.PMID: 12271374 [PubMed - indexed for MEDLINE]Related articles

Recurrent corneal ulcerations with perforation in keratosis follicularis (Darier-White disease).

Mielke J, Grüb M, Besch D, Schlote T.

Br J Ophthalmol. 2002 Oct;86(10):1192-3. No abstract available. PMID: 12234910 [PubMed - indexed for MEDLINE]Related articlesFree article

Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations.

Fauser S, Luberichs J, Besch D, Leo-Kottler B.

Biochem Biophys Res Commun. 2002 Jul 12;295(2):342-7.PMID: 12150954 [PubMed - indexed for MEDLINE]Related articles

Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.

Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E.

Vision Res. 2002 May;42(11):1475-83.PMID: 12044753 [PubMed - indexed for MEDLINE]Related articles

Visual field constriction and electrophysiological changes associated with vigabatrin.

Besch D, Kurtenbach A, Apfelstedt-Sylla E, Sadowski B, Dennig D, Asenbauer C, Zrenner E, Schiefer U.

Doc Ophthalmol. 2002 Mar;104(2):151-70.PMID: 11999623 [PubMed - indexed for MEDLINE]Related articles

A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy.

Luberichs J, Leo-Kottler B, Besch D, Fauser S.

Graefes Arch Clin Exp Ophthalmol. 2002 Feb;240(2):96-100.PMID: 11931086 [PubMed - indexed for MEDLINE]Related articles

Alterations of slow and fast rod ERG signals in patients with molecularly confirmed Stargardt disease type 1.

Scholl HP, Besch D, Vonthein R, Weber BH, Apfelstedt-Sylla E.

Invest Ophthalmol Vis Sci. 2002 Apr;43(4):1248-56.PMID: 11923272 [PubMed - indexed for MEDLINE]Related articlesFree article

[Evaluation of extensive visual field defects with computer-assisted kinetic perimetry]

Schiefer U, Schiller J, Paetzold J, Dietrich TJ, Vonthein R, Besch D.

Klin Monbl Augenheilkd. 2001 Jan;218(1):13-20. German. PMID: 11225394 [PubMed - indexed for MEDLINE]Related articles

[Carcinoma-associated retinopathy: a review with clinical examples]

Sobottka B, Schlote T, Besch D, Djelebova T, Wilhelm H, Zrenner E.

Klin Monbl Augenheilkd. 2000 Jan;216(1):17-24. Review. German. PMID: 10702938 [PubMed - indexed for MEDLINE]Related articles

[A case of Leber optic neuropathy with a new point mutation in the cytochrome b gene]

Besch D, Wissinger B, Zrenner E, Leo-Kotter B.

Ophthalmologe. 2000 Jan;97(1):22-6. German. PMID: 10663786 [PubMed - indexed for MEDLINE]Related articles

Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.

Besch D, Leo-Kottler B, Zrenner E, Wissinger B.

Graefes Arch Clin Exp Ophthalmol. 1999 Sep;237(9):745-52.PMID: 10447650 [PubMed - indexed for MEDLINE]Related articles

The role of the peripherin/RDS gene in retinal dystrophies.

Kohl S, Giddings I, Besch D, Apfelstedt-Sylla E, Zrenner E, Wissinger B.

Acta Anat (Basel). 1998;162(2-3):75-84. Review.PMID: 9831753 [PubMed - indexed for MEDLINE]Related articles

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

Wissinger B, Besch D, Baumann B, Fauser S, Christ-Adler M, Jurklies B, Zrenner E, Leo-Kottler B.

Biochem Biophys Res Commun. 1997 May 19;234(2):511-5.PMID: 9177303 [PubMed - indexed for MEDLINE]Related articles

Detection and elimination of contaminations interfering with the determination of zinc in plasma.

Reimold EW, Besch DJ.

Clin Chem. 1978 Apr;24(4):675-80.PMID: 639274 [PubMed - indexed for MEDLINE]Related articlesFree article