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There are 8412495 results for: content related to: Macular lesion resembling adult-onset vitelliform macular dystrophy in Kearns–Sayre syndrome with multiple mtDNA deletions

  1. Endocrine dysfunction in Kearns-Sayre syndrome

    Clinical Endocrinology

    Volume 37, Issue 1, July 1992, Pages: 97–104, J. N. Harvey and D. Barnett

    Version of Record online : 17 MAR 2008, DOI: 10.1111/j.1365-2265.1992.tb02289.x

  2. Kearns-sayre syndrome: Biochemical studies of mitochondrial metabolism

    Annals of Neurology

    Volume 24, Issue 5, November 1988, Pages: 630–637, M. E. Martens, P. L. Peterson, Dr. C. P. Lee, M. A. Nigro, Z. Hart, M. Glasberg, J. S. Hatfield and C. H. Chang

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410240507

  3. Sinus Dysrhythmia in Kearns-Sayre Syndrome

    Pacing and Clinical Electrophysiology

    Volume 17, Issue 5, May 1994, Pages: 991–994, KARL S. ULICNY Jr., FRANK C. DETTERBECK and COLIN D. HALL

    Version of Record online : 30 JUN 2006, DOI: 10.1111/j.1540-8159.1994.tb01445.x

  4. Lumping or splitting? “ophthalmoplegia-plus” or kearns-sayre syndrome?

    Annals of Neurology

    Volume 1, Issue 1, January 1977, Pages: 37–54, R. A. Berenberg, J. M. Pellock, S. DiMauro, D. L. Schotlan, E. Bonilla, A. Eastwood, A. Hays, C. T. Vicale, M. Behrens, A. Chutorian and Dr. L. P. Rowland

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410010104

  5. You have free access to this content
    Progression of Conduction System Disease in a Paced Patient With Kearns-Sayre Syndrome

    Clinical Cardiology

    Volume 32, Issue 6, June 2009, Pages: E64–E66, Murat Yeşil, Serdar Bayata, Nursen Postaci and Erdinç Arikan

    Version of Record online : 20 MAR 2009, DOI: 10.1002/clc.20242

  6. Kearns-sayre syndrome with reduced plasma and cerebrospinal fluid folate

    Annals of Neurology

    Volume 13, Issue 6, June 1983, Pages: 679–682, Dr Richard J. Allen, Salvatore DiMauro, David L. Coulter, Alexander Papadimitriou and Sheldon P. Rothenberg

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410130620

  7. Kearns-Sayre syndrome: Unusual pattern of expression of subunits of the respiratory chain in the cerebellar system

    Annals of Neurology

    Volume 45, Issue 3, March 1999, Pages: 377–383, Kurenai Tanji, Tuan H. Vu, Eric A. Schon, Salvatore DiMauro and Eduardo Bonilla

    Version of Record online : 31 MAY 2001, DOI: 10.1002/1531-8249(199903)45:3<377::AID-ANA14>3.0.CO;2-M

  8. Progressive Sensorineural Hearing Loss in Children With Mitochondrial Encephalomyopathies

    The Laryngoscope

    Volume 111, Issue 3, March 2001, Pages: 515–521, Priv. Doz. Petra Zwirner and Ekkehard Wilichowski

    Version of Record online : 2 JAN 2009, DOI: 10.1097/00005537-200103000-00024

  9. You have free access to this content
    Inhalation anaesthesia and the Kearns-Sayre syndrome


    Volume 49, Issue 10, October 1994, Pages: 876–878, M. H. LAUWERS, C. VAN LERSBERGHE and F. CAMU

    Version of Record online : 22 FEB 2007, DOI: 10.1111/j.1365-2044.1994.tb04263.x

  10. You have free access to this content
    Multiple mtDNA deletions in Kearns-Sayre syndrome associated with macular dystrophy

    Acta Ophthalmologica


    Version of Record online : 11 AUG 2011, DOI: 10.1111/j.1755-3768.2011.268.x

  11. A case of hypopituitarism accompanying Kearns–Sayre syndrome treated with human chorionic gonadotropin: A case report and literature review


    Volume 49, Issue 8, October 2017, Y.-X. Kang, Y.-J. Wang, Q. Zhang, X.-H. Pang and W. Gu

    Version of Record online : 6 OCT 2016, DOI: 10.1111/and.12711

  12. Kearns-Sayre Syndrome with hypoparathyroidism

    Annals of Neurology

    Volume 3, Issue 6, June 1978, Pages: 513–518, Samuel J. Horwitz and Uros Roessmann

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410030611

  13. High proportions of mtDNA duplications in patients with Kearns-Sayre syndrome occur in the heart

    American Journal of Medical Genetics

    Volume 71, Issue 4, 5 September 1997, Pages: 443–452, Bernard Fromenty, Rosalba Carrozzo, Sara Shanske and Eric A. Schon

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19970905)71:4<443::AID-AJMG14>3.0.CO;2-G

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    Asymmetric septal hypertrophy in kearns-sayre syndrome

    Clinical Cardiology

    Volume 7, Issue 11, November 1984, Pages: 603–605, M. Kupari

    Version of Record online : 4 FEB 2009, DOI: 10.1002/clc.4960071109

  15. Kearns-Sayre Syndrome: A Case Report and Review of Cardiovascular Complications

    Pacing and Clinical Electrophysiology

    Volume 28, Issue 5, May 2005, Pages: 454–457, TIMOTHY J. YOUNG, AMIT K. SHAH, MUN HENG LEE and DAVID L. HAYES

    Version of Record online : 3 MAY 2005, DOI: 10.1111/j.1540-8159.2005.40049.x

  16. Kearns-Sayre syndrome and hypoparathyroidism

    Annals of Neurology

    Volume 3, Issue 5, May 1978, Pages: 455–458, J. M. Pellock, M. Behrens, L. Lewis, D. Holub, S. Cartter and L. P. Rowland

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410030519

  17. Progressive cytochrome c oxidase deficiency in a case of earns-sayre syndrome: Morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues

    Annals of Neurology

    Volume 21, Issue 6, June 1987, Pages: 564–572, Dr. Nereo Bresolin, Maurizio Moggio, Luciano Bet, Andrea Gallanti, Alessandro Prelle, Eduardo Nobile-Orazio, Laura Adobbati, Claudio Ferrante, Giulio Pellegrini and Guglielmo Scarlato

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410210607

  18. Anaesthesia and the Kearns-Sayre syndrome

    Pediatric Anesthesia

    Volume 3, Issue 5, September 1993, Pages: 307–311, R. ESTES, B. GINSBERG and E.C. BLOCH

    Version of Record online : 30 JAN 2007, DOI: 10.1111/j.1460-9592.1993.tb00094.x

  19. Demyelinating radiculopathy in the kearns-sayre syndrome: A clinicopathological study

    Annals of Neurology

    Volume 8, Issue 4, October 1980, Pages: 373–380, Dennis R. Groothuis, Sidney Schulman, Robert Wollman, James Frey and Nicholas A. Vick

    Version of Record online : 7 OCT 2004, DOI: 10.1002/ana.410080406

  20. Familial childhood onset neuropathy and cirrhosis with the 4977bp mitochondrial DNA deletion

    American Journal of Medical Genetics

    Volume 111, Issue 2, 1 August 2002, Pages: 191–194, D.G.M. McDonald, J.B. McMenamin, M.A. Farrell, O. Droogan and A.J. Green

    Version of Record online : 19 JUN 2002, DOI: 10.1002/ajmg.10522