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    Results: 41

    1.

    [Intermittent elevation deficiency]

    van Waveren M, Jägle H.

    Ophthalmologe. 2009 Aug;106(8):746-9. German. PMID: 19593572 [PubMed - indexed for MEDLINE]Related articles

    2.

    Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.

    Kitiratschky VB, Behnen P, Kellner U, Heckenlively JR, Zrenner E, Jägle H, Kohl S, Wissinger B, Koch KW.

    Hum Mutat. 2009 Aug;30(8):E782-96.PMID: 19459154 [PubMed - indexed for MEDLINE]Related articles

    3.

    The dependence of luminous efficiency on chromatic adaptation.

    Stockman A, Jägle H, Pirzer M, Sharpe LT.

    J Vis. 2008 Dec 15;8(16):1.1-26.PMID: 19146268 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    [Fulminant process of an orbital Mucoracea infection]

    Jägle C, Papageorgiou E, Preyer S, Löwenheim H, Schiefer U, Jägle H.

    Ophthalmologe. 2009 Jun;106(6):547-50. German. PMID: 18709374 [PubMed - indexed for MEDLINE]Related articles

    5.

    Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation.

    Kitiratschky VB, Nagy D, Zabel T, Zrenner E, Wissinger B, Kohl S, Jägle H.

    Br J Ophthalmol. 2008 Aug;92(8):1086-91.PMID: 18653602 [PubMed - indexed for MEDLINE]Related articles

    6.

    Long-term follow-up of retinitis pigmentosa patients with multifocal electroretinography.

    Nagy D, Schönfisch B, Zrenner E, Jägle H.

    Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4664-71. Epub 2008 Jun 19.PMID: 18566474 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.

    Kitiratschky VB, Grau T, Bernd A, Zrenner E, Jägle H, Renner AB, Kellner U, Rudolph G, Jacobson SG, Cideciyan AV, Schaich S, Kohl S, Wissinger B.

    Eur J Hum Genet. 2008 Jul;16(7):812-9. Epub 2008 Feb 20.PMID: 18285826 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.

    Wissinger B, Dangel S, Jägle H, Hansen L, Baumann B, Rudolph G, Wolf C, Bonin M, Koeppen K, Ladewig T, Kohl S, Zrenner E, Rosenberg T.

    Invest Ophthalmol Vis Sci. 2008 Feb;49(2):751-7.PMID: 18235024 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    The multifocal pattern electroretinogram (mfPERG) and cone-isolating stimuli.

    Langrová H, Jägle H, Zrenner E, Kurtenbach A.

    Vis Neurosci. 2007 Nov-Dec;24(6):805-16.PMID: 18093368 [PubMed - indexed for MEDLINE]Related articles

    10.

    Safety profile of a taurine containing irrigation solution (AcriProTect) in pars plana vitrectomy.

    Yoeruek E, Jägle H, Lüke M, Grisanti S, Warga M, Krott R, Spitzer MS, Tatar O, Bartz-Schmidt KU, Szurman P.

    Retina. 2007 Nov-Dec;27(9):1286-91.PMID: 18046239 [PubMed - indexed for MEDLINE]Related articles

    11.

    [How to distinguish between autosomal dominant optic atrophy and Leber's hereditary optic neuropathy]

    Leo-Kottler B, Jägle H, Küpker T, Schimpf S.

    Ophthalmologe. 2007 Dec;104(12):1060-5. German. PMID: 17899121 [PubMed - indexed for MEDLINE]Related articles

    12.

    [Multifocal oscillatory potentials (mfOPs) in patients with central retinal vein occlusion]

    Stepień JA, Jagle H, Kurtenbach A, Stepień MW, Omulecki W.

    Klin Oczna. 2006;108(10-12):424-30. Polish. PMID: 17455719 [PubMed - indexed for MEDLINE]Related articles

    13.

    L:M-cone ratio estimates of the outer and inner retina and its impact on sex differences in ERG amplitudes.

    Jägle H, Heine J, Kurtenbach A.

    Doc Ophthalmol. 2006 Sep;113(2):105-13. Epub 2006 Sep 19.PMID: 17047907 [PubMed - indexed for MEDLINE]Related articles

    14.

    Hyperoxia, hyperglycemia, and photoreceptor sensitivity in normal and diabetic subjects.

    Kurtenbach A, Mayser HM, Jägle H, Fritsche A, Zrenner E.

    Vis Neurosci. 2006 May-Aug;23(3-4):651-61.PMID: 16962009 [PubMed - indexed for MEDLINE]Related articles

    15.

    Advantages and disadvantages of human dichromacy.

    Sharpe LT, de Luca E, Hansen T, Jägle H, Gegenfurtner KR.

    J Vis. 2006 Mar 7;6(3):213-23.PMID: 16643091 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    A luminous efficiency function, V*(lambda), for daylight adaptation.

    Sharpe LT, Stockman A, Jagla W, Jägle H.

    J Vis. 2005 Dec 21;5(11):948-68.PMID: 16441195 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Dose-dependency and time-course of electrophysiologic short-term effects of VIAGRA: a case study.

    Jägle H, Jägle C, Sèrey L, Sharpe LT.

    Doc Ophthalmol. 2005 Mar-May;110(2-3):247-54.PMID: 16328933 [PubMed - indexed for MEDLINE]Related articles

    18.

    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

    19.

    Visual acuity and X-linked color blindness.

    Jägle H, de Luca E, Serey L, Bach M, Sharpe LT.

    Graefes Arch Clin Exp Ophthalmol. 2006 Apr;244(4):447-53. Epub 2005 Aug 23.PMID: 16133025 [PubMed - indexed for MEDLINE]Related articles

    20.

    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

    21.

    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

    22.

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

    Kohl S, Varsanyi B, Antunes GA, Baumann B, Hoyng CB, Jägle H, Rosenberg T, Kellner U, Lorenz B, Salati R, Jurklies B, Farkas A, Andreasson S, Weleber RG, Jacobson SG, Rudolph G, Castellan C, Dollfus H, Legius E, Anastasi M, Bitoun P, Lev D, Sieving PA, Munier FL, Zrenner E, Sharpe LT, Cremers FP, Wissinger B.

    Eur J Hum Genet. 2005 Mar;13(3):302-8.PMID: 15657609 [PubMed - indexed for MEDLINE]Related articlesFree article

    23.

    Multifocal electroretinogram in trichromat and dichromat observers under cone isolating conditions.

    Kurtenbach A, Heine J, Jägle H.

    Vis Neurosci. 2004 May-Jun;21(3):249-55.PMID: 15518196 [PubMed - indexed for MEDLINE]Related articles

    24.

    [Color vision and the diagnosis of reduced visual acuity]

    Jägle H.

    Klin Monbl Augenheilkd. 2004 Sep;221(9):739-42. German. PMID: 15459839 [PubMed - indexed for MEDLINE]Related articles

    25.

    The Nagel anomaloscope: its calibration and recommendations for diagnosis and research.

    Jägle H, Pirzer M, Sharpe LT.

    Graefes Arch Clin Exp Ophthalmol. 2005 Jan;243(1):26-32. Epub 2004 Jul 31.PMID: 15290149 [PubMed - indexed for MEDLINE]Related articles

    26.

    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

    27.

    Molecular basis of an inherited form of incomplete achromatopsia.

    Tränkner D, Jägle H, Kohl S, Apfelstedt-Sylla E, Sharpe LT, Kaupp UB, Zrenner E, Seifert R, Wissinger B.

    J Neurosci. 2004 Jan 7;24(1):138-47.PMID: 14715947 [PubMed - indexed for MEDLINE]Related articlesFree article

    28.

    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

    29.

    The multifocal electroretinogram (mfERG) and cone isolating stimuli: variation in L- and M-cone driven signals across the retina.

    Albrecht J, Jägle H, Hood DC, Sharpe LT.

    J Vis. 2002;2(8):543-58.PMID: 12678638 [PubMed - indexed for MEDLINE]Related articlesFree article

    30.

    The multifocal visual evoked potential and cone-isolating stimuli: implications for L- to M-cone ratios and normalization.

    Hood DC, Yu AL, Zhang X, Albrecht J, Jägle H, Sharpe LT.

    J Vis. 2002;2(2):178-89.PMID: 12678591 [PubMed - indexed for MEDLINE]Related articlesFree article

    31.

    Detecting color vision in a malingerer.

    Jägle H, Sadowski B, Kremers J, Scholl HP, Leo-Kottler B, Sharpe LT.

    Doc Ophthalmol. 2003 Mar;106(2):121-8.PMID: 12678276 [PubMed - indexed for MEDLINE]Related articles

    32.

    Reorganization of human cortical maps caused by inherited photoreceptor abnormalities.

    Baseler HA, Brewer AA, Sharpe LT, Morland AB, Jägle H, Wandell BA.

    Nat Neurosci. 2002 Apr;5(4):364-70.PMID: 11914722 [PubMed - indexed for MEDLINE]Related articles

    33.

    The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes.

    Jagla WM, Jägle H, Hayashi T, Sharpe LT, Deeb SS.

    Hum Mol Genet. 2002 Jan 1;11(1):23-32.PMID: 11772996 [PubMed - indexed for MEDLINE]Related articlesFree article

    34.

    CNGA3 mutations in hereditary cone photoreceptor disorders.

    Wissinger B, Gamer D, Jägle H, Giorda R, Marx T, Mayer S, Tippmann S, Broghammer M, Jurklies B, Rosenberg T, Jacobson SG, Sener EC, Tatlipinar S, Hoyng CB, Castellan C, Bitoun P, Andreasson S, Rudolph G, Kellner U, Lorenz B, Wolff G, Verellen-Dumoulin C, Schwartz M, Cremers FP, Apfelstedt-Sylla E, Zrenner E, Salati R, Sharpe LT, Kohl S.

    Am J Hum Genet. 2001 Oct;69(4):722-37. Epub 2001 Aug 30.PMID: 11536077 [PubMed - indexed for MEDLINE]Related articlesFree article

    35.

    Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.

    Kohl S, Baumann B, Broghammer M, Jägle H, Sieving P, Kellner U, Spegal R, Anastasi M, Zrenner E, Sharpe LT, Wissinger B.

    Hum Mol Genet. 2000 Sep 1;9(14):2107-16.PMID: 10958649 [PubMed - indexed for MEDLINE]Related articlesFree article

    36.

    L, M and L-M hybrid cone photopigments in man: deriving lambda max from flicker photometric spectral sensitivities.

    Sharpe LT, Stockman A, Jägle H, Knau H, Nathans J.

    Vision Res. 1999 Oct;39(21):3513-25.PMID: 10746123 [PubMed - indexed for MEDLINE]Related articles

    37.

    Macular pigment densities derived from central and peripheral spectral sensitivity differences.

    Sharpe LT, Stockman A, Knau H, Jägle H.

    Vision Res. 1998 Nov;38(21):3233-9.PMID: 9893831 [PubMed - indexed for MEDLINE]Related articles

    38.

    Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivities.

    Sharpe LT, Stockman A, Jägle H, Knau H, Klausen G, Reitner A, Nathans J.

    J Neurosci. 1998 Dec 1;18(23):10053-69.PMID: 9822760 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.

    Wissinger B, Jägle H, Kohl S, Broghammer M, Baumann B, Hanna DB, Hedels C, Apfelstedt-Sylla E, Randazzo G, Jacobson SG, Zrenner E, Sharpe LT.

    Genomics. 1998 Aug 1;51(3):325-31.PMID: 9721202 [PubMed - indexed for MEDLINE]Related articles

    40.

    Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.

    Kohl S, Marx T, Giddings I, Jägle H, Jacobson SG, Apfelstedt-Sylla E, Zrenner E, Sharpe LT, Wissinger B.

    Nat Genet. 1998 Jul;19(3):257-9.PMID: 9662398 [PubMed - indexed for MEDLINE]Related articles

    41.

    [Report on dental assistants' education course in dental education center in Stuttgart]

    Jägle H.

    Quintessenz J. 1985 Dec;15(12):1091-4. German. No abstract available. PMID: 3869705 [PubMed - indexed for MEDLINE]Related articles

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