Zoekresultaten - John R. Heckenlively

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  1. 1
    Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa.

    Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa. door John R. Heckenlively

    Gepubliceerd in 1982
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  2. 2
    Frequency of Anti-Retinal Antibodies in Normal Human Serum

    Frequency of Anti-Retinal Antibodies in Normal Human Serum door Kaori Shimazaki, Guy V. Jirawuthiworavong, John R. Heckenlively, Lynn K. Gordon

    Gepubliceerd in 2008
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  3. 3
    Síndrome de Menkes: novos achados oculares

    Síndrome de Menkes: novos achados oculares door Rosane C. Ferreira, John R. Heckenlively, John H. Menkes, J. Bronwyn Bateman

    Gepubliceerd in 1997
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  4. 4
    Autoimmunity in hereditary retinal degenerations. II. Clinical studies: antiretinal antibodies and fluorescein angiogram findings.

    Autoimmunity in hereditary retinal degenerations. II. Clinical studies: antiretinal antibodies and fluorescein angiogram findings. door John R. Heckenlively, Alfred M. Solish, Susan M. Chant, Roberta H. Meyers-Elliott

    Gepubliceerd in 1985
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  5. 5
    Surgical management of retinal detachment associated with the acute retinal necrosis syndrome.

    Surgical management of retinal detachment associated with the acute retinal necrosis syndrome. door H. Richard McDonald, Hilel Lewis, Allan E. Kreiger, Yossi Sidikaro, John R. Heckenlively

    Gepubliceerd in 1991
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  6. 6
    Melanoma-Associated Retinopathy

    Melanoma-Associated Retinopathy door Ying Lu, Lin Jia, Shirley He, Mary C. Hurley, Monique Leys, Thiran Jayasundera, John R. Heckenlively

    Gepubliceerd in 2009
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  7. 7
    Mutations in the PDE6B Gene in Autosomal Recessive Retinitis Pigmentosa

    Mutations in the PDE6B Gene in Autosomal Recessive Retinitis Pigmentosa door Michael Danciger, JOHN BLANEY, Yong Gao, Danyang Zhao, John R. Heckenlively, Samuel G. Jacobson, Debora B. Farber

    Gepubliceerd in 1995
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  8. 8
    Diurnal variations of foveoschisis by optical coherence tomography in patients with <i>RS1</i> X-linked juvenile retinoschisis

    Diurnal variations of foveoschisis by optical coherence tomography in patients with <i>RS1</i> X-linked juvenile retinoschisis door Maria Fernanda Abalem, David C. Musch, David G. Birch, Mark E. Pennesi, John R. Heckenlively, Thiran Jayasundera

    Gepubliceerd in 2018
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  9. 9
    RP2 Phenotype and Pathogenetic Correlations in X-Linked Retinitis Pigmentosa

    RP2 Phenotype and Pathogenetic Correlations in X-Linked Retinitis Pigmentosa door Thiran Jayasundera, Kari Branham, Mohammad Othman, William Rhoades, Athanasios J. Karoukis, Hemant Khanna, Anand Swaroop, John R. Heckenlively

    Gepubliceerd in 2010
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  10. 10
    Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

    Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15. door John R. Heckenlively, Bo Chang, Lawrence C. Erway, Peng Chen, N. L. Hawes, Gregory S. Hageman, Thomas H. Roderick

    Gepubliceerd in 1995
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  11. 11
    Clinical and Electrophysiologic Characterization of Paraneoplastic and Autoimmune Retinopathies Associated With Antienolase Antibodies

    Clinical and Electrophysiologic Characterization of Paraneoplastic and Autoimmune Retinopathies Associated With Antienolase Antibodies door Richard G. Weleber, Robert C. Watzke, William T. Shults, Karmen M Trzupek, John R. Heckenlively, Robert A. Egan, Grazyna Adamus

    Gepubliceerd in 2005
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  12. 12
    Rescue of retinal degeneration by intravitreally injected adult bone marrow–derived lineage-negative hematopoietic stem cells

    Rescue of retinal degeneration by intravitreally injected adult bone marrow–derived lineage-negative hematopoietic stem cells door Atsushi Otani, Michael I. Dorrell, Karen Kinder, Stacey K. Moreno, Steven Nusinowitz, Eyal Banin, John R. Heckenlively, Martin Friedlander

    Gepubliceerd in 2004
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  13. 13
    Rescue of retinal degeneration by intravitreally injected adult bone marrow–derived lineage-negative hematopoietic stem cells

    Rescue of retinal degeneration by intravitreally injected adult bone marrow–derived lineage-negative hematopoietic stem cells door Atsushi Otani, Michael I. Dorrell, Karen Kinder, Stacey K. Moreno, Steven Nusinowitz, Eyal Banin, John R. Heckenlively, Martin Friedlander

    Gepubliceerd in 2004
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  14. 14
    Mutations in the<i>GUCA1A</i>gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase

    Mutations in the<i>GUCA1A</i>gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase door Veronique Kitiratschky, Petra Behnen, Ulrich Kellner, John R. Heckenlively, Eberhart Zrenner, Herbert Jägle, Susanne Kohl, Bernd Wissinger, Karl‐Wilhelm Koch

    Gepubliceerd in 2009
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  15. 15
    Double hyperautofluorescent ring on fundus autofluorescence in <i>ABCA4</i>

    Double hyperautofluorescent ring on fundus autofluorescence in <i>ABCA4</i> door Maria Fernanda Abalem, Cynthia X. Qian, Kari Branham, Dana Schlegel, Abigail T. Fahim, Naheed W. Khan, John R. Heckenlively, Thiran Jayasundera

    Gepubliceerd in 2017
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  16. 16
    Genotype–phenotype correlation in 440 patients with NPHP-related ciliopathies

    Genotype–phenotype correlation in 440 patients with NPHP-related ciliopathies door Moumita Chaki, Julia Hoefele, Susan J. Allen, Gokul Ramaswami, Sabine Janssen, Carsten Bergmann, John R. Heckenlively, Edgar A. Otto, Friedhelm Hildebrandt

    Gepubliceerd in 2011
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  17. 17
    The Need for Standardization of Antiretinal Antibody Detection and Measurement

    The Need for Standardization of Antiretinal Antibody Detection and Measurement door Farzin Forooghian, Ian M. MacDonald, John R. Heckenlively, Elise Héon, Lynn K. Gordon, John J. Hooks, Barbara Detrick, Robert B. Nussenblatt

    Gepubliceerd in 2008
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  18. 18
    Ablation of the X-Linked Retinitis Pigmentosa 2 (<i>Rp2</i>) Gene in Mice Results in Opsin Mislocalization and Photoreceptor Degeneration

    Ablation of the X-Linked Retinitis Pigmentosa 2 (<i>Rp2</i>) Gene in Mice Results in Opsin Mislocalization and Photoreceptor Degeneration door Linjing Li, Naheed W. Khan, Toby W. Hurd, Amiya K. Ghosh, Christiana L. Cheng, Robert S. Molday, John R. Heckenlively, Anand Swaroop, Hemant Khanna

    Gepubliceerd in 2013
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  19. 19
    A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene

    A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene door Melanie M. Sohocki, Lori S. Sullivan, Helen A. Mintz-Hittner, David G. Birch, John R. Heckenlively, Carol L. Freund, Roderick R. McInnes, Stephen P. Daiger

    Gepubliceerd in 1998
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  20. 20
    Mutations in the X-Linked Retinitis Pigmentosa Genes<i>RPGR</i>and<i>RP2</i>Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa

    Mutations in the X-Linked Retinitis Pigmentosa Genes<i>RPGR</i>and<i>RP2</i>Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa door Jennifer D. Churchill, Sara J. Bowne, Lori S. Sullivan, Richard A. Lewis, Dianna K. Wheaton, David G. Birch, Kari Branham, John R. Heckenlively, Stephen P. Daiger

    Gepubliceerd in 2013
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